Glossary | Science Diversity

Glossary

Hypermedia Glossary Of Genetic Terms – Birgid Schlindwein’s

Birgid Schlindwein’s

Hypermedia Glossary Of Genetic Terms

Alphabetical list of all 670 items of the glossary

A
Acentric
Acrocentric
Adaptation
Adaptive landscape
Adaptive peak
Adaptive radiation
Adaptive surface
Adaptive value
Addition line
Additive genetic variance
Adenine
Adenosine
AFLP
Alien addition line
Allele
Allele frequency
Allele specific associated primer
Allele specific oligo
Allele specific polymerase chain reaction
Alloenzyme
Allogamy
Alloploidy
Allopolyploidy
Allosome
Allosyndesis
Allotetraploidy
Allozygote
Alpha helix
Altruism
Amino acid
Amphidiploidy
Amphimixis
Amplification
Amplified fragment length polymorphism
Anagenesis
Anaphase
Aneuploidy
Anlage
Anneal
Anticodon
Antisense strand
Apogamy
Apomixis
AP-PCR
Arbitrarily primed polymerase chain reaction
Arbitrary primer
Arrayed library
ARS
ASAP
ASO
AS-PCR
Assortative mating
Autogamy
Autonomous replication sequence
Autopolyploidy
Autoradiography
Autosome
Autozygote
BAC
Back-cross
Bacterial artificial chromosome
Bacteriophage
Base pair
Base sequence
Base sequence analysis
Bioinformatics
Biotechnology
Bivalent
Blotting
bp
Breakpoint
Breed
Breeding line
Bridging cross
Bud
Budding
Bulk selection
Bulked segregant analysis
C
CAPS
Carboxyl terminus
CCAAT box
cDNA
cDNA library
Cell cycle
Cell division
Centimorgan
Central dogma
Centromere
Centromere interference
Character
Chiasma
Chiasma interference
Chimera
Chloroplast
Chloroplast DNA
Chromatid
Chromatin
Chromomere
Chromoneme
Chromosomal address
Chromosome
Chromosome jumping
Chromosome walking
Cis
Cistron
Clade
Cladogenesis
Class
Cleaved amplified polymorphic sequence
Clone
Clone bank
Cloning
Cloning vector
cM
Code
Codominance
Codon
Coefficient of coancestry
Coefficient of inbreeding
Coefficient of parentage
Coefficient of relationship
Comparative mapping
Complementary DNA
Complementary RNA
Complementary sequence
Complementation
Complementation test
Complete linkage
Compound heterozygote
Conjugation
Consanguinity
Consensus sequence
Conserved sequence
Contig
Contig map
Contiguous gene syndrome
Convergence
Convergent evolution
Conversion
COP
Co-segregation
Cosmid
Coupling
cpDNA
CpG island
Cre-loxP system
cRNA
Cross breeding
Crossing
Crossing over
Cultivar
Cytogenetics
Cytology
Cytoplasm
Cytosine
DAF
DAMD
Darwinian fitness
Deficiency
Deletion
Deme
Denature
Denaturing gradient gel electrophoresis
Denaturing high-performance liquid chromatography
Deoxyribonucleic acid
Deoxyribonucleotide
DGGE
DHPLC
Diakinesis
Dicentric
Dichogamy
Dihybrid cross
Dioecious
Diploid
Diplotene
Directed amplification of minisatellite region DNA
Disassortative mating
DNA
DNA amplification fingerprinting
DNA clone
DNA fingerprinting
DNA polymerase
DNA probes
DNA replication
DNA sequence
DNA typing
Domain
Dominance variance
Dominant
Double helix
Downstream
Duplication
Dysgenic
Ectopic
Electrophoresis
Electroporation
Endonuclease
Endosperm
Enhancer
Environment
Environmental variance
Enzyme
Epigenesis
Epigenetic
Episome
Epistasis
Epistatic
Escherichia coli
EST
Euchromatin
Eugenics
Eukaryote
Euploidy
Evolution
Evolutionarily conserved
Exogenous DNA
Exon
Exonuclease
Expressed gene
Expressed sequence tag
Expressivity
F1
F2
Family
Family selection
Fecundity
Fecundity selection
Fertilization
Filial generation
FISH
Fitness
Fixed allele
Flanking region
Flow cytometry
Flow karyotyping
Fluorescence in situ hybridization
Founder effect
Frameshift
Frameshift mutation
G
Gamete
Gametic selection
GBA
G-banding
Geitonogamy
Gene
Gene cluster
Gene dose
Gene expression
Gene family
Gene flow
Gene interaction
Gene library
Gene map
Gene mapping
Gene pool
Gene product
Gene targeting
Gene transfer
Genetic bit analysis
Genetic code
Genetic distance
Genetic diversity
Genetic drift
Genetic engineering
Genetic engineering technologies
Genetic fine structure
Genetic interference
Genetic map
Genetic material
Genetic variance
Genetics
Genome
Genome project
Genomic DNA
Genomic in situ hybridization
Genomic library
Genoplasm
Genotype
Genus
Germ line
Germ line mosaicism
Germplasm
Giemsa banding
Giemsa stain
GISH
Guanine
Haploid
Haploinsufficiency
Haplotype
Hardy-Weinberg equilibrium
Hemizygous
Hereditary
Heredity
Heritability
Herkogamy
Hermaphrodite
Heterochromatin
Heterochromosome
Heteroduplex analysis
Heteroduplex DNA
Heterokaryon
Heteroplasmy
Heterosome
Heterostyly
Heterozygosity
Heterozygote
Histone
Homeobox
Homoduplex DNA
Homokaryon
Homologous chromosome
Homologous recombination
Homology
Homoplasy
Homozygosity
Homozygote
Human gene therapy
Human Genome Initiative
Hybrid
Hybridization
Hydrogen bond
Hypostasis
Hypostatic
Identity
Imprinting
in silico
In situ hybridization
In vitro
In vivo
Inbreeding
Inbreeding coefficient
Inbreeding depression
Incomplete dominance
Informatics
Inheritance
Insert
Insertion
Insertion sequence
Interchange
Interference
Intergenic
Intergenic DNA
Intergenic region
Interkinesis
Interphase
Inter-simple sequence repeat
Intragenic
Intron
Intron boundary skidding
Inverse polymerase chain reaction
Inversion
Inverted repeat
IPCR
IS element
Isoenzyme
Isozyme
ISSR
Karyotype
kb
Kilobase
Kinetochore
Large single copy
Leptotene
Lethal gene
Library
Ligation
Lineage
Linkage
Linkage disequilibrium
Linkage equilibrium
Linkage group
Linkage map
Localize
Loci
Locus
LOD score
m.u.
MAAL
MAAP
Macroevolution
Macrorestriction map
Map Unit
Mapping
Marker
Maternal inheritance
Mating
Mating frequency
Mating system
Mating type
Matroclinous inheritance
Mb
Megabase
Meiosis
Meme
Mendel
Mendel’s first law
Mendel’s second law
Messenger RNA
Metacentric
Metaphase
Methylation
Microsatellite
Migration
Minisatellite
Mispairing
Mitochondria
mitochondrial DNA
Mitosis
Monoclonal
Monoecious
Monogenic
Monohybrid cross
Monosom
Mosaicism
Motif
mRNA
mtDNA
Multifactorial disorder
Multigenic disorder
Multiple allelism
Multiple arbitrary amplicon profiling
Multiplexing
Mutation
Mutator mutation
Natural selection
Negative interference
Neo-darwinism
Nick translation
Nitrogenous base
Nondisjunction
Non-linkage
Nonsense mutation
Northern blotting
Nuclease
Nucleic acid
Nucleolus
Nucleoside
Nucleosome
Nucleotide
Nucleus
Offspring
Oligonucleotide
Oncogene
Ontogeny
Open reading frame
Operator
Operon
Order
ORF
Origin
Orthology
Outbreeding
Overlapping clones
Ovum
P1-derived artificial chromosome
PAC
Pachytene
packaging RNA
Paired box
Panmixia
Parallel evolution
Parallelism
Paralogy
Parthenogenesis
Partial linkage
PCR
PCR-RFLP
Pedigree
Penetrance
Peptide
Permutation
Phage
Phenotype
Phenotypic variance
Phylogenesis
Phylon
Physical map
Plasmid
Plastid
Pleiotropy
Point mutation
Pollination
Poly A RNA
Polyamine
Polygenic
Polygenic disorders
Polymerase chain reaction
Polymorphism
Polypeptide
Polyploid
Polytene
Population
Positional cloning
Positive interference
Postmeiotic Segregation
Preformation
Pribnow box
Primer
Primordium
pRNA
Probability
Probe
Progeny
Prokaryote
Promoter
Prophase
Protein
Proteome
Proteomics
Pseudogene
Pure-breeding
Purine
Pyrimidine
QTL
Quantitative trait
Quantitative trait loci
Random mating
Randomly amplified polymorphic DNA
RAPD
Rare-cutter enzyme
Reading frame
Recessive
Reciprocal cross
Recombinant clone
Recombinant DNA molecule
Recombinant DNA techniques
Recombinase
Recombination
Recombination frequency
Regulatory region
Regulatory sequence
repetitive DNA
Replication
Replicon
Reproduction
Repulsion
Resolution
Restriction enzyme
Restriction enzyme cutting site
Restriction fragment
Restriction fragment length polymorphism
Restriction landmark genomic scanning
Restriction map
Restriction site
Retrotransposon
Retrovirus
Reversal
Reverse transcriptase
Reverse transcription
RFLP
Ribonucleic acid
Ribonucleotides
Ribosomal RNA
Ribosome
RLGS
RNA
RNA polymerase
RNA splicing
rRNA
Satellite DNA
SCAR
SDS-PAGE
Segregation
Segregation distortion
Selection
Self-incompatibility
Selfing
Self-pollination
Self-sterility
Semi-conservative
Sequence
Sequence characterised amplified region
Sequence tagged microsatellite
Sequence tagged site
Sequencing
Sex chromosome
Shotgun method
Similarity
Simple sequence repeat
Single nucleotide polymorphism
Single primer amplification reaction
Single stranded conformational polymorphism
Single-gene disorder
Site
Small single copy
SNP
Somaclonal variation
Somatic cell
Somatic hybrid
Southern blotting
SPAR
Speciation
Species
Sperm
Spireme
Spore
SSCP
SSR
Stasigenesis
STMS
Stop codon
Strain
Strand
Structural change
Strucutural gene
STS
Survival
Synapsis
Synapton
Synaptonemal complex
Syndesis
Synteny
T
Tandem repeat sequence
TATA box
Taxon
Technology transfer
Telomerase
Telomere
Telophase
Template
Termination codon
Terminator
Test-cross
Tetrad
TGGE
Thermal gel gradient electrophoresis
Thymine
Trait
Trans
Transcript
Transcription
Transcription start site
Transduction
Transfection
Transfer RNA
Transformation
Transgenic
Transition
Translation
Translocation
Transposable element
Transposase
Transposition
Transposon
Transversion
Trisomy
tRNA
True-breeding
U
Undermethylation
Upstream
Uracil
Variable-number tandem-repeat
Variation
Variety
Vector
Viability
Virus
VNTR
Western blotting
Wild-type
Xenogamy
YAC
Yeast artificial chromosome
Zygote
Zygotene

Web source : http://hal.weihenstephan.de/genglos/asp/genreq.asp?list=1

Abortive transduction
An event where the fragment of DNA introduced by transduction fails to be recombined into the recipient chromosome and because the DNA fragment lacks an origin of replication it is only inherited by one of the daughter cells at each cell division.

Acrylamide
Used to make polyacrylamide gels for separation of macromolecules by electrophoresis. Polyacrylamide gels are produced by polymerization of acrylamide into linear chains and cross-linking the acrylamide chains with bis-acrylamide (N,N’-methylene-bis-acrylamide). Polymerization is initiated by adding ammonium persulfate and the reaction is accelerated by TEMED (N,N,N’,N’-tetramethylethylenediamine) which catalyzes the formation of free radicals from ammonium persulfate. Acrylamide gels are generally poured between glass plates because oxygen inhibits the polymerization because oxygen radicals formed can interact with acrylamide and terminate chain elongation.

Activator
A gene product (usually protein) that positively regulates transcription. Activators may either increase binding of RNA polymerase to the promoter (closed complex formation) or stimulate RNA polymerase to begin transcription (open complex formation).

Active site
The region of an enzyme responsible for catalysis.

Adaption
The ability to physiologically adjust to a new environment while exposed to that particular environment. Typically cells de-adapt when transferred to different growth conditions.

Adenosine triphosphate (ATP)
A compound with high energy phosphate bonds that provide the energy for many cellular processes.

Aerobic
The presence of oxygen. Often used to describe an organism that requires oxygen for growth or growth conditions with oxygen.

Affinity
The strength of an interaction between two molecules, such as the binding of an antigen to an antibody.

Agarose
An uncharged polysaccharide purified from agar. Agarose melts when heated to 100 C and resolidifies when cooled below about 50°C. When it solidifies agarose forms a matrix. The size of the pores in the gel matrix can be varied by using different concentrations of agarose: the higher the concentration of agarose, the smaller the pore size.

Alkylating agent
An organic compound able to transfer an alkyl group to nucleotides.

Alleles
Alternative forms of a gene. For example, the mutants putA601 and putA736 each have a different mutation in the putA gene.

Allele specific suppressor
A second-site mutation that repairs the mutant phenotype but only in strains with certain, specific mutations at the first-site.

Allosteric
The stereospecific modification of a protein by an effector to influence the activity of another site of the protein.

Alpha-complementation
The ability of a short N-terminal fragment of beta-galactosidase to interact with the C-terminal portion of beta-galactosidase to form a functional enzyme.

Amber codon
The UAG nonsense codon. This is one of the three normal chain termination or stop codons that does not code for any amino add in the universal code.

Amber mutation
A mutation that creats an amber codon (UAG) from a different codon.

Amber suppressor
A mutant tRNA gene that recognizes the UAG codon but is aminoacylated and inserts the amino acid at the corresponding position in the growing polypeptide.

Ames test
A genetic test for the identification of carcinogens based upon their mutagenic activity initially developed by Bruce Ames. The test relies upon the ability of a chemical or physical agent to promote the reversion of different classes of mutations that cause histidine auxotrophy.

Amino acid analog
See analog.

Ampicillin (Amp)
An antibiotic that inhibits crosslinking of peptidoglycan chains in the cell wall of eubacteria. Cells growing in the presence of ampicillin synthesize weak cell walls, causing them to burst due to the high internal osmotic pressure. Amp resistance encoded by most transposons and plasmids is due to a periplasmic Beta-lactamase that breaks the Beta-lactam ring of ampicillin. Ampicillin is a derivative of penicillin.

Anaerobic
The absence of oxygen. Often used to describe an organism that is sensitive to oxygen or growth conditions without oxygen.

Analog (or the British spelling Analogue)
A chemical that is similar, but not identical, to another chemical. For example, thioproline is an analog of the amino acid proline, and azaguanine is an analog of the nucleotide guanine. Certain analogs are toxic and can be used to select for mutants that affect the synthesis or metabolism of the corresponding compound.

Angstrom
A unit of measurement that was widely used until recently to describe molecular dimensions, but the unit nanometer (nm) is now more commonly used. One angstrom equals 10 nm.

Antigenic drift
The accumulation of mutations that modify a molecule on the cell surface of a pathogen and thereby alters recognition by the host immune system. These changes prevent preexisting antibodies from recognizing the invading pathogen. This process is most often used to describe viruses. (See Antigenic variation below)

Antigenic variation
A change in the types or amounts of a molecule on the cell surface of a pathogen that alters recognition by the host immune system. Antigenic variation can occur by altering a variety of surface molecules including proteins and carbohydrates. There are many molecular mechanisms for antigenic variation, including inversion, recombination between multiple casettes, and hypermutation. Antigenic variation occurs in eukaryotic microbes (e.g. Trypanosomes), bacteria (e.g. Neisseria gonorrhoeae, and Salmonella enterica), and viruses. The change in surface antigens due to mutation, recombination, or chromosome reassortment in viruses is called antigenic drift.

Annealing
Pairing of a single-stranded nucleic acid with the complementary strand to form a duplex.

Antibiotic
A substance that interfers with a particular step of cellular metabolism, causing either bactericidal or bacteriostatic inhibition; sometimes restricted to those having a natural biological origin.

Antibody
A protein complex that specifically interacts with an antigen.

Anticodon
The three bases in a tRNA that are complementary to those in the codon of the mRNA.

Antigen
A substance that interacts with an antibody.

Antimutator
A mutation that decreases the overall mutation rate, often by modifying DNA polymerase.

Antisense RNA
An RNA molecule that can hybridize to an mRNA molecule. Hybridization of an antisense RNA molecule to the translation start sites on an mRNA prevents the initiation of translation. For example, an antisense RNA is involved in the regulation of transposase expression from Tn10.

Anti-terminator
A protein that allows RNA polymerase to continue transcription through a transcription termination site.

AP endonuclease
An endonuclease which recognizes an AP site and cuts the defective strand on the 5′ side of the missing base.

AP site
A molecule of single-stranded or double-stranded DNA missing a purine or pyrimidine base.

Aporepressor
A protein that requires binding of a small molecule co-repressor to negatively regulate gene expression.

Apurinic or apyrimidinic (AP) site
A molecule of single-stranded or double-stranded DNA missing a purine or pyrimidine base.

Apoptosis
Cell death due to a intracellular developmental program or induced by other cells.

A priori
Deduced from first principles; without prior knowledge.

Archae
One of the three domains of living organisms: Archae, Bacteria, and Eukarya. Although they share a basic morphology with bacteria and they are also prokaryotes (i.e. they lack a nuclear membrane), in many molecular details they resemble eukaryotes more than bacteria. Previously called Archaebacteria. First described by Carl Woese at the University of Illinois.

A site
The binding site for the aminoacyl-tRNA on the ribosome.

Atoll
A region of DNA that is absent on the chromosome of an organism but absent from closely related organisms (i.e., the opposite of a genetic island). The loss of such genetic material may confer a distinctive phenotype. For example, absence of certain genes from E. coli enhances virulence.

Attachment site (att)
The specific sequences on phage (attP) and bacterial (attB) chromosomes between which site-specific recombination occurs in order to integrate the phage genome into the bacterial chromosome.

Attenuation
A mechanism of regulating the level of transcription by interfering with mRNA elongation. Slowed translation through a regulatory region allows formation of a RNA secondary structure that promotes transcription termination. Requires coupled transcription and translation and thus is restricted to prokaryotes. Two examples of genes regulated by attenuation include the trp and his operons in E. coli.

Attenuator
A region of leader mRNA that can form alternative secondary structures that determine whether transcription is terminated or proceeds into downstream genes. See Attenuation.

Att site
See attachment site.

Autogenous regulation (autoregulation)
The gene product that controls its own expression. See autogenous repressor.

Autogenous repressor
The product of a regulator gene which binds to its own operator and prevents transcription of the associated structural genes.

Autoradiography
A photographic image produced exposing photographic film to a radiolabeled molecule (e.g. DNA, RNA, or protein). The emissions from the radioactive label expose the photographic film.

Autoregulation
See autogenous regulation.

Autotroph
An organism which does not require any organic carbon for its energy source or for its growth.

Auxotroph
A mutant that will only grow when a particular nutritional requirement (e.g. amino acid, nucleotide, or vitamin) is provided.

Auxotrophic requirement
A nutritional supplement required for growth of an auxotrophic strain.

Avidin
A protein that binds biotin with a very high affinity. Used for the detection of biotinylated probes.
ß-galactosidase
An enzyme that catalyzes the cleavage of lactose into glucose + galactose. In E. coli this enzyme is encoded by the lacZ gene. Often used as a reporter for assaying gene expression (see X-gal).

ß-lactam antibiotics
Antibiotics taht contain a ß-lactam ring and act by inhibiting peptidoglycan synthesis. For example, penicillins, cephalosporins, and related antibiotics.

ß-lactamase
An enzyme that cleaves the ß-lactam ring of ß-lactam antibiotics, thus inactivating the antibiotics. The ampicillin resistance encoded by many common plasmids is due to a secreted ß-lactamase.

BAC
An acronym for Bacterial Artifical Chromosome. Low copy number plasmid vectors that allow stable cloning very large DNA fragments (often 100 Kb or more).

Backcross
A genetic cross between an offspring and one of its parents or an organism genetically identical to one of its parents.

Back mutation
A reversion event which restores the original DNA sequence.

Bacteriophage (or simply Phage)
A virus that infects a bacterium.

Bacteriostatic
A condition which prevents the growth of bacteria without killing them.

Baculovirus
A virus that has been used as a cloning vector for the production of recombinant protein in insect cells.

Base analog
A purine or pyrimidine base that differs slightly in structure from the normal bases found in DNA or RNA. Some analogs may be incorporated into nucleic acids in place of the normal base, often resulting in a base substitution mutation. Some examples include aminopurine, azaguanine, azauracil, and 5-bromodeoxyuridine.

Base pair
A complementary purine and pyrimidine that are hydrogen-bonded to form double-stranded DNA or RNA.

Base substitution mutation
A mutation resulting in the replacement of one base for a different base.

Batch culture
Growth of bacteria in a fixed volume of liquid medium in a closed vessel, with no additions or removals made during the period of incubation.

Bidirectional replication
Two replication forks proceed in opposite directions from the same origin of replication. Sometimes called omega-replication.

Bioinformatics
The management and analysis of data (especially DNA sequence data) using advanced computing techniques. Bioinformatics is an important field of genomics research, because of the complexity of searching and comparing the large number of DNA sequences generated.

Biolistics
A means of introducing DNA into cells that involves bombardment with high-velocity microprojectiles coated with DNA.

Biological containment
One of the precautionary measures taken to prevent the replication of recombinant DNA molecules in microorganisms in the natural environment. Biological containment involves the use of vectors and host organisms that have been modified so that they will not survive outside of the laboratory.

Biotechnology
The use of living organisms (often microbes) in industrial processes.

Biotin
A molecule that can be incorporated into dUTP and used as a non-radioactive label for a DNA probe.

Blunt (flush) end
The end of a DNA molecule at which both strands terminate at the same nucleotide position with no single-stranded extension.

Branch migration
A “zipper-like” pairing of two homologous DNA strands during genetic recombination.

Broad host range
The ability to infect and reproduce in a wide variety of different organisms. For example, a phage or plasmid that can grow in many different bacterial species, or a bacterium that can produce disease in many different eukaryotic hosts.

Broth culture
Microorganisms grown in a liquid medium.

Buoyant density
The density possessed by a molecule or particle when suspended in an aqueous salt or sugar solution.

Burst size
The average number of phage released from a single infected bacterium during lytic growth. The burst size depends upon both the phage itself and the growth conditions of the bacteria. The burst size for characterized phage varies from only a few progeny phage per bacterium to over a hundred progeny phage per bacterium.

Bypass suppressor
A second site mutation that activates a new pathway that eliminates the need for the original mutant pathway. For an example of bypass suppression, see the argE suppression of proline biosynthesis mutants.
CAP (Catabolite activator protein)
See CRP.

Capsduction
A DNA transfer system in Rhodobacter capsulatus where the donor DNA is carried in a phage-like structure known as a gene transfer agent (GTA). The donor DNA derived from the GTA-producing cells can enter a recipient cell and recombine with th e recipient genome.

Capsid
The protein layer that encloses the nucleic acid of a phage or virus and protects it from the environment.

Carbon source
A nutrient which provides the carbon required for cellular biosynthesis.

Carcinogen
A physical or chemical agent that causes cancer.

Cascade
A series of events that result in transmission and usually amplification of a weak signal.

Cassette
A gene fragment that can be cloned into a site to confer some property. For example, cassettes encoding antibiotic resistance are often used to disrupt a cloned gene.

Catabolite repression
A global regulatory system resulting in decreased expression of many genes due to the addition of an efficient carbon source such as glucose. Characteristically mediated by a complex between the CRP protein and cAMP in enteric bacteria.

Catenane
A circular DNA molecule with two or more interlinked rings.

CCC
An abbreviation for “circular, covalently closed” DNA molecules.

cDNA Cloning
A technique involving reverse transcription of purified mRNA into the corresponding complementary DNA prior to insertion into a vector.

Cell extract
A preparation consisting of a large number of broken cells and their released contents.

Cell-free translation system
A cell extract containing all the components required for protem synthesis (i.e. ribosomal subunits, tRNAs, amino acids, enzymes and cofactors) and able to translate added mRNA molecules.

Centromere
The region of a eukaryotic chromosome responsible for attachment to the mitotic or meiotic spindle leading to controlled partitioning of chromosomes during nuclear division.

Chain-termination (“nonsense” or “stop”) codon
A codon signalling the termination of polypeptide synthesis. The three standard stop codons are UAG (amber), UAA (ochre), and UGA (opal).

Chaperone
A protein that facilitates the folding of other proteins or assembly of multi-protein complexes.

Chelator
A substance that binds particular ions, removing them from solution. Some chelators are relatively nonspecific, binding to a variety of ions with similar charge, and other chelators bind much more strongly to specific ions. A few examples include the divalent ion chelators citrate and EDTA, the calcium chelator EGTA, and the iron chelator desferrioxamine. For more about chelators, see: http://www.sigmaaldrich.com/Brands/Fluka___Riedel_Home/Bioscience/BioChemika_Ultra/Chelators.html.

Chemotaxis
A behavorial response of cells resulting in movement toward or away from to a chemical stimulus.

Chi site
An 8-nucleotide DNA sequence (5′ GCTGGTGG 3′) which is a hot-spot for homologous recombination. When the RecBCD exonuclease encounters a chi site the RecD subunit is released and the RecBC complex then functions as a helicase, unwinding the DNA and providing single stranded which can invade a homologous region of double-stranded DNA. Chi sites typically occur about once every 5 kb on the chromosomes of enteric bacteria and most are oriented in the same direction as DNA replication.

Chiasma
A cross-over between strands of two non-sister chromatids during recombination. The junction where two homologous chromosomes appear to exchange genetic material during recombination. (Chi is the greek letter c which resembles a genetic cross-over.)

Chimeric plasmid
A plasmid used in gene cloning and constructed from two or more different plasmids.

Chloramphenicol (Cam)
An antibiotic that inhibits protein synthesis by binding to the 50s ribosomal subunit and blocking the peptidyltransferase reaction. Chloramphenicol resistance encoded by many plasmids (e.g. pBR328) is due to a cytoplasmic chloramphenicol acyltransferase which inactivates chloramphenicol by covalently acetylating it.

Chromatid
One of the two identical strands of a newly replicated chromosome.

Chromogenic substrate
A substrate that changes color when modified by a specific enzyme.

Chromosome
A self-replicating DNA molecule that carries essential genetic information for growth and replication of a cell or virus. The DNA organized into a tightly packaged structure by associated histone-like proteins in bacteria and histones in eukaryotes. (The chromosomes of some viruses contain RNA instead of DNA.)

Chromosome walking
A technique used to identify a series of overlapping restriction fragments, often to determine the relative positions of genes on large chromosomes.

Circularly permuted DNA
A population of linear DNA molecules produced as if by breaking open circular molecules at different points.

cis
Two genes located are on the same molecule of DNA (commonly refers to genes that are located very close to each other on the same DNA molecule).

Cis-trans test
A genetic test to determine whether two mutations are in the same or in different genes.

Cis-dominance
A mutation that prevents the expression of downstream genes. Polar mutations in an operon are typically cis-dominant.

Cistron
An obsolete term for a gene. Often used to refer to the number of genes encoded by a single transcript; monocistronic refers to a transcript that encodes one gene, and polycistronic refers to a transcript that encodes multiple genes.

Cleared lysate
A cell extract that has been centrifuged to remove cell debris, subcellular particles, and much of the chromosomal DNA.

Clonal
A population of cells derived from a single cell and thus expected to be genetically identical. Genetic differences in a “clonal” population may arise from random spontaneous mutations during growth of the cells.

Clone
Cells derived from a single cell and thus expected to be genetically identical.

Cloning
The production of multiple, genetically identical molecules of DNA, cells, or organisms.

Cloning vector
A DNA molecule that is capable of replication in a suitable host cell, that has suitable site(s) for the insertion of DNA fragments by recombinant DNA techniques, and that has genetic markers that allow selection for the vector in a host cell.

Coding region
A sequence of DNA that encodes a polypeptide.

Codominance
The observation of a phenotype caused by independent expression of both alleles of a gene in a diploid.

Codon
The three consecutive nucleotides (triplets) in DNA or RNA that encode a particular amino acid or signal the termination of polypeptide synthesis.

Cohesive ends
Single-stranded complementary sequences at two ends of a DNA molecule (examples include the ends of the linear phage lambda chromosome, and the ends resulting from digestion of DNA with many restriction endonucleases).

Coinheritance frequency
The ratio of recombinants that acquire both the selected and unselected marker vs the total number of recombinants.

Cointegrate
A circular molecule of DNA formed during replicative transposition by joining two separate circular replicons. The resulting structure has two copies of the transposon, one at each junction point, orientated in direct repeats.

Colinearity
The linear correspondance between the nucleotide sequence and the order of amino acids in a polypeptide chain.

Cold sensitive mutant
A mutation that results in a gene product that is active at a high temperature (e.g. 42°C) but inactive at low temperatures (e.g. 30°C). Cold sensitive mutations often affect hydrophobic interactions between protein complexes or between proteins and membrane componants.

Cold spot
Sites within a gene (or genome)Êat which mutations occur with much lower frequency than at other sites.

Colicin
A polypeptide secreted by bacteria which inhibit or prevent the growth of related bacteria which lack the corresponding colicin immunity proteins. Colicins are encoded by a group of naturally occurring plasmids first found in E. coli (e.g., the Col E1 plasmid). Colicins kill other bacteria by a variety of mechanisms depending on the type of colicin — some colicins block protein synthesis, some colicins induce the degradation of chromosomal DNA, some colicins form transmembrane holes in the cytoplasmic membrane, etc.

Colinear
Markers that occur in a sequential order in a DNA or protein sequence.

Coliphage
A phage that infects Escherichia coli.

Colony
A visible group of cells arising from a single cell plated on solid medium.

Colony blots
See Colony hybridization.

Colony hybridization
Use of in situ hybridization with a labeled nucleotide probe to identify bacterial colonies that contain DNA sequences homologous to a probe.

Colony PCR
Use of a bacterial colony for direct polymerase chain reaction to amplify a specific nucleotide sequence.

Coorperativity
For DNA binding proteins, cooperativity generally refers to the increased binding of a protein to a DNA site due to the prior binding of another protein nearby. (Note that more rigorous definations of cooperativity are sometimes used in biochemistry to refer to binding of small molecules, that can result in positive cooperativity (enhanced binding) and negative cooperativity (poorer binding) of a second molecule following binding of a first molecule.)

Coordinate gene expression
Transcription of a group of genes at the same time due to a common regulatory mechanism.

Compatibility
The ability of two different types of plasmid to coexist in the same cell.

Competence
The transient physiological state required for a bacterial cell to take up transforming DNA.

Complementary
Two polynucleotide chains that can base-pair to form a double-stranded molecule.

Complementation
The ability of a gene to produce a functional gene product which compensates for the mutant phenotype caused by a mutation in another gene. Typically, the complementing gene produces a gene product (e.g. a repressor protein or an enzyme for synthesis of a metabolite) that is diffusible and thus functions in trans.

Complex
Containing multiple macromolecules in an organized structure. For example, the RecBCD proteins form a complex that functions as an exonuclease and this activity requires all three of the proteins to function together.

Composite transposon
A transposible element flanked by two copies of an IS element.

Concatamer
An end-to-end (tandem) array of identical DNA rnolecules; a repeated polymer of DNA.

Conditional lethal mutant
A mutant that can grow under one set (permissive) of environmental conditions but dies under different (restrictive or nonpermissive) conditions.

Conditional mutant
A mutant that can grow under one set (permissive) of environmental conditions but cannot grow under different (restrictive or nonpermissive) conditions. Some conditional mutants survive under the nonpermissive conditions but others (conditional lethal mutants) die under the nonpermissive conditions.

Congenic
Strains that are identical except for a small region of the chromosome.

Congression
The uptake of more than one transforming DNA fragment by a single competent cell (occurs most often when a high concentration of transforming DNA is available).

Conjugation
The establishment of a bridge between a donor and a recipient cell and the transfer of DNA from one cell to the other. Conjugation is mediated by certain plasmids and transposons. Conjugation requires direct contact between the donor and recipient cells.

Conjugative plasmid
A bacterial plasmid that encodes functions required for conjugation.

Conjugative transposon
A transposon that encodes functions required for conjugation.

Consensus sequence
A idealized nucleotide sequence that represents a sequence that serves some particular function (e.g. a promoter) at multiple places in a genome. Each position of the consensus sequence represents the nucleotide most often found at that position in the real sequences. The precise sequence will vary from site to site, but they all are similar to the consensus sequence.

Conservative (nonreplicative) transposition
A transposition event where the transposable element is lost from its original location and inserted at a new location.

Conserved sequence
A nucleotide or protein sequence which is shared between different regions or organisms, typically because the sequence fulfills an important function (e.g. a DNA-binding site or protein motif) and thus is retained during evolution.

Constitutive gene expression
A gene or operon which is expressed at all times independant of the environmental conditions.

Contig
A set of DNA fragments that overlap to yield a continuous sequence without gaps.

Continuous culture
The culture of microorganisms in liquid medium under controlled conditions, with regular additions of depleted nutrients and removal of excreted metabolites from the medium over a lengthy period of time.

Copy number
The number of molecules of a particular plasmid present in a bacterium.

Co-repressor
A small molecule that binds to an aporepressor protein, producing a conformational change that causes it to function as a transcriptional repressor.

Cos site
The sequence that is cut to produce the cohesive, single-stranded extensions located at the ends of the linear DNA molecules of certain phages (e.g. lambda).

Cosanguine
Related by a common ancestor.

Cosmid
A cloning vector consisting of the phage lambda cos site inserted into a plasmid. Such vectors can be packaged into lambda phage or maintained as plasmids. Cosmids are often used to clone large DNA fragments (up to about 40 kilobases).

Cotransduction
Homologous recombination of two closely linked genes or two mutations within the same gene and brought into a cell on the same fragment of transducing DNA.

Cotransformation
The simultaneous uptake of two genetic markers via transformation. Cotransformation of two markers occurs at a frequency greater than 50 percent indicates that the two markers are genetically linked.

Counterselection
A condition that prevents growth of the donor in a genetic cross.

Covalently closed-circular (CCC)
A completely double-stranded circular DNA molecule, with no nicks or discontinuities, usually with a supercoiled conformation.

CRM
Cross reacting material. A molecule that reacts with an antibody. A common test for the presence of an inactive protein in cells.

Cross-feeding
Growth of a mutant stimulated by metabolites released by another cell.

Cross-over
The site where two homologous DNA strands originating from homologous chromosomes are resealed to form the recombinant chromosome. The reciprocal exchange of genetic material to produce genetic recombinants. Sometimes abbreviated as X-over.

Cross reacting material
See CRM.

CRP
Catabolite receptor protein, also called CAP or catabolite activator protein. The interaction of CRP with cAMP modulates many aspects of catabolite repression in enteric bacteria.

Cryptic
A function that is silent. For example, a cryptic gene may have an intact coding sequence but lack an active promoter. Cryptic functions can be turned on by an appropriate mutation.

C-terminus
The end of a polypeptide chain that has a free carboxylic acid (-COOH) group.

Curing
A treatment that promotes the loss of a resident prophage or plasmid from a cell. For example, acridine orange is sometimes used to cure bacteria of a plasmid.

Cut and paste
Jargon for the excision of a DNA fragment from one molecule and insertion into another DNA molecule. Commonly used to describe cloning a DNA fragment by cleavage with a restriction enzyme and ligation into a vector. Also used to describe transposition mechanisms where the transposon is excised from one DNA molecule and inserted into a second DNA molecule without replication of the transposon.

Cyclic AMP (cAMP)
An adenosine monophosphate molecule with the phosphate covalently attached to both the 3′ and 5′ carbons of the ribose.
D-loop (displacement loop)
A structure formed when one strand of a duplex DNA molecule is displaced by a single-strand of homologous invading DNA. This reaction is catalyzed by the RecA protein in bacteria.

Defective phage
A phage that lacks one or more functions that are required for reproduction.

Defined medium
A bacterial growth medium in which all the components are known. Typically only includes the minimal growth requirements.

Deletion
The loss of one or more bases or base pairs from a molecule of DNA.

Deletion mapping
The use of deletion mutations to determine the position of overlapping point mutations for fine structure mapping of a genetic locus.

Denaturation of proteins
The unfolding of a protein molecule, usually by high temperatures or ionic detergents such as sodium dodecyl sulfate (SDS).

Denaturation of DNA or RNA
Separation of the two strands of a double-stranded DNA or RNA molecule by disrupting the hydrogen bonds that join the complementary bases from the two opposite strands, usually by heat or alkali. (Often called “melting”.)

Density shift labeling
The addition of either a heavy or a light isotope to the growth medium which changes the density of the newly synthesized nucleic acids. For example, N14 is the natural isotope of nitrogen, so incorporation of N15 into DNA incr eases the density of the DNA.

Density-gradient centrifugation
Separation of molecules and particles on the basis of buoyant density, by centrifugation in a concentrated sucrose or caesium chloride solution.

Deoxyribonucleic acid
See DNA.

Derepression
The release of a gene or operon from repression so that it is expressed (or turned on).

Diauxic growth
A biphasic growth curve, typically resulting from the sequential use of multiple nutrients (e.g. glucose utilization followed by lactose utilization).

Dideoxynucleotide
A modified nucleotide that lacks the 3′ hydroxyl group, preventing further chain elongation when incorporated into a growing polynucleotide.

Diploid
An organism which contains pairs of each chromosome.

Direct repeats
Two identical (or nearly identical) nucleotide sequences sometimes separated by a sequence of non-repeated DNA. For example, 3' TAGT . . . TAGT 5'
5' ATCA . . . ATCA 3'

Directed evolution
This term is used in two ways. (i) A laboratory process using mechanisms of natural selection to produce mutants adaptated to defined environmental challenges. This approach can be used to produce adaptions in single molecules, such as a RNA molecule or an enzyme. Since chemical reaction can occur very fast, multiple “generations” of molecules can be produced quickly. Microorganisms such as bacteria can also reproduce quickly, allowing multiple generations of selection in a short period of time. This approach has been used to produce novel enzymes with industrial and biomedical applications, and to produce bacteria with potential bioremediation applications. (i) The concept that under certain stressful conditions, there is a selection for those mutational changes that favor survival. This controversial concept, also called adaptive evolution, is essentially a molecular version of Lamarkian evolution.

Double-strand break (DSB)
A cut through both strands of the DNA backbone, resulting in two exposed double-stranded ends.

DNA (deoxyribonucleic acid)
A macromolecule usually made up of two antiparallel polynucleotide strands held together by weak hydrogen bonds and with deoxyribose as the component sugar.

DNA gyrase
A topoisomerase that removes supercoils from DNA by first producing double-strand breaks and then sealing them.

DNA ligase
The enzyme that joins the 5′ and 3′ ends of polynucleotide chains by the formation of a phosphodiester bond between them.

D-loop (displacement loop)
The structure formed when ssDNA pairs with a dsDNA molecule, disrupting the pairing of the original duplex DNA to form a hybrid between the ssDNA and one of the strands of the duplex DNA, and displacing the other strand from the duplex.

DNA polymerases
Enzymes that polymerize deoxyribonucleotides onto an existing polynucleotide chain using the complementary strand of DNA as a template.

DNA primase
The enzyme that normally synthesizes the RNA primers required for initiating DNA synthesis.

DNA Repair
A variety of different mechanisms that remove or modify damaged DNA.

DNase
An enzyme that degrades DNA.

dNTP
Deoxynucleotide triphosphates used in the synthesis of DNA — deoxy-ATP, deoxy-TTP, deoxy-GTP, or deoxy-CTP.

Domain
A discrete, independantly folded region of a protein. Different functions of a multifunctional protein are usually localized in separate domains.

Dominant
The phenotype that is observed when two alleles of a gene are present in a cell. The gene whose phenotype is expressed is the dominant allele and the allele whose phenotype is masked is the recessive allele. If the phenotype of the diploid is inte rmediate between that of the two haploid genes, then the alleles are co-dominant.

Donor
The source of DNA in a genetic cross. For example, the transducing phage brought into a bacterial cell.

Downstream
A sequence located after a particular site relative to the direction of transcription and translation (i.e. located to the 3′ side of a particular site). For example, the lacZ structural gene is located downstream of the lac promoter.

Double digestion
Cleavage of a DNA molecule with two different restriction endonucleases, either concurrently or consecutively.

Duplex DNA
A double-stranded DNA molecule.

Duplication
A region of DNA that is present in two copies. The DNA is present as an adjacent, direct repeat in tandem duplications. It is also possible for the duplicated DNA to be present at distant sites on a chromosome.

dUTPase
An enzyme which degrades dUTP to prevent the incorpation of dU into DNA.
Eclipse period
The period of time after infection with a virus during which new virions are formed, but not released (contrast with latent period).

Electrophoresis
Separation of molecules on the basis of their net electric charge.

Electrophoresis of DNA
DNA fragments have a constant charge/length ratio due to the net negative charge of the phosphate backbone. Therefore, DNA migrates toward the (+) electrode. The rate of migration of linear DNA mainly depends on the pore size of the gel and length of the DNA. During electrophoresis DNA molecules seem to “snake” through the pores in the gel “head first”. As the pore size decreases (i.e. the agarose or acrylamide concentration increases) it is harder for longer DNA molecules to orient properly to snake through the pores: smaller DNA fragments snake through the pores easier and hence migrate faster. Thus, the rate of migration of linear double stranded DNA is inversely proportional to the log of its molecular weight. By using gels with different concentrations of agarose or acrylamide, a wide range of DNA fragment sizes can be separated. The shape of the DNA molecule also affects its ability to snake through the pores in the gel. In general features that make the DNA less flexible or less compact slow the migration in a gel. The rate of migration of different forms of plasmid DNA is usually: supercoiled > linear > nicked circles. In addition, secondary structure and bends in linear DNA may affect the rate of migration.

Electroporation
A method for transferring DNA (or other small molecules) into cells by exposure to a rapid pulse of high voltage, which causes the transient formation of small pores in the cell membrane.

Elongation factor
A protein that facilitates protein synthesis.

Endonuclease
An enzyme that makes breaks in a molecule of DNA by hydrolyzing internal phosphodiester bonds. An endonuclease may be specific for either single or double stranded DNA or RNA.

Endospore
A metabolically inactive, nonreplicating form of certain bacteria, including the genera Bacillus and Clostridium. Endospores tend to be highly resistant to physical and chemical damage.

Enhancer
A cis-acting regulatory sequence that can increase transcription from an adjacent promoter.

Enrichment
A condition which increases the proportion of a particular organism or mutant strain from a mixed population. For example, a penicillin enrichment kills growing cells and allows mutants unable to grow under a particular condition to survive; however, for each round of penicillin enrichment typically only 1% of the growing cells are killed, thus each round of enrichment increases the mutant ratio about 100-fold. Compare with “selection”.

Epigenetic
The inheritance of a particular trait that is not encoded in the nucleotide sequence. For example, methylation of certain DNA sequences can influence gene expression, and the methylation pattern may be maintained following DNA synthesis by preferential methylation of hemimethylated sequences.

Episome
A genetic element that can exist either as an autonomous replicating plasmid or can insert into the bacterial chromosome. This is an old term that is rarely used anymore. Such elements are simply called plasmids (for example, F-prime plasmid).

Epistasis
A condition where one gene masks the expression of another gene. For example, if there are two mutations that affect a single metabolic pathway, a mutation that disrupts the gene product which acts at an earlier step in the pathway will usually obscure the mutation that affects a later step in the pathway.

Epitope
A portion of an antigen recognized by an antibody binding site. For protein antigens the epitope is typically 5-8 amino acids. Gene fusions to epitopes can be used as a tag to recognize specific proteins.

Error prone repair
A mechanism for repair of DNA damage that often results in mutations (e.g. SOS repair).

Ethanol precipitation
Precipitation of nucleic acid molecules by ethanol plus salt. Commonly used to concentrate DNA from aqueous solutions.

Ethidium bromide
A fluorescent chemical that intercalates between base pairs in a doublestranded DNA molecule. Commonly used to detect DNA following gel electrophoresis. Ethidium bromide intercalates between the stacked bases of DNA and RNA. When excited by UV light between 254 nm (short wave) and 366 nm (long wave) it emits fluorescent light at 590 nm. Due to the decreased rotation possible when it is intercalated, the DNA-ethidium bromide complex produces about 50 times more fluorescence than free ethidium bromide. When ethidium bromide stained gels are photographed on a UV transilluminator a UV filter is required to screen out the background UV from the transilluminator. Ethidium bromide is a known carcinogen.

Eucaryote
An organism with a nuclear membrane and membrane bound organelles (e.g. mitochondria), and a mitotic spindle. This group of organisms is more correctly called Eucarya.

Excision repair
A repair system that removes nucleotides from a damaged strand of DNA and then replaces them with a new tract of DNA synthesised using the undamaged complementary strand as a template.

Exon
The sequence in a spliced gene that is retained after removal of the introns to provide the mature mRNA that is translated by the ribosome.

Exonuclease
An enzyme that digests a molecule of nucleic acid by removing successive nucleotides from the 5′ or 3′ end. Exonucleases may be specific for single or double stranded DNA or RNA, and may be specific for either 3′ or 5′ ends.

Expression vector
A cloning vector designed so that a foreign gene inserted into the vector will be expressed in the host organism. The inserted DNA is often placed under the control of a strong, regulatable promoter (e.g. the lacZ or araBAD promoter) so that expression of the gene product will only occur when desired.

Extragenic
An affect due to a second gene. For example, an extragenic suppressor is a mutation in a second gene that repairs the mutant phenotype.
Facultative
Organisms that can grow under different conditions. Commonly used to describe bacteria that can grow oxidatively under aerobic or fermentatively under anaerobic conditions.

F-factor
An E. coli plasmid that encodes conjugative transfer (“fertility”) functions. The F-plasmid may exist as an autonomous plasmid in the cytoplasm or may integrate into specific sites in the chromosome, producing an Hfr cell.

F+ cell
A cell that carries a F-factor as an autonomous plasmid, which enables the cell acting as a donor (male) to transfer the F-factor to a recipient (female) cell.

F- cell
A cell which does not contain the F-factor, and hence able to act as a recipient (female) in a conjugative DNA transfer in matings with F+ or Hfr strains.

Fimbriae
Thin, proteinaceous filaments that extend from the cell surface of microbial cells and facilate adhesion to solid surfaces or other cells.

Fingerprinting
A common term for methods that allow the rapid identification of particular types of bacteria (also known as “typing”). For example, plasmid fingerprinting involves determining the number and types of plasmids in a particular strain of bacteria.

F-pilus
A filamentous appendage encoded by the F-plasmid. The pilus promotes adhesion of F+ and F- cells and provides adsorption sites for male-specific phages.

F-prime (F’)
An extrachromosomal F-plasmid that carries a fragment of chromosomal DNA.

Filamentous phage
A group of phage with the nucleic acid surrounded by a long, tubular protein coat. Examples of filaments phage include M13 and Ff.

Filter mating
A method where conjugation between donor and recipient bacteria is done on a millipore filter. Conjugation is often much more efficient on a solid surface, probably because the donor and recipient bacteria are fixed in close proximity facilitating stable mating bridge formation.

Flagella
Long, flexible, helical protein structures that extend from the surface of the cell. Rotation of flagella in one direction results in motility, and rotation of flagella in the opposite direction results in tumbling.

Flanking sequence or flanking region
The DNA sequence located on either side of a specific genetic locus.

Fluctuation Test
An experimental approach designed by Luria and Delbruck to determine whether mutations are random or directed, and to measure mutation rates (see http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/mutations/fluctuation.html).

Footprinting
A method for identification of a protein-binding site on a DNA molecule. For example, DNase I footprinting identifies those phosphodiester bonds which are covered by a specific DNA-binding protein and thus protected from cleavage by DNase I.

Frameshift
A mutation which adds or deletes one or two base pairs (or any non-multiple of 3) from a coding sequence in a molecule of DNA, so that the genetic code is read out-of-phase. All codons translated downstream of a frameshift mutation will be misread, and frequently an out-of-frame stop codon will prematurely terminate translation.
Functional domain
A region of a polypeptide chain or RNA that performs a particular function. Functional domains are often folded into independant structures, separated from the rest of the polymer by a flexible hinge region.
Gel electrophoresis
The process of separating charged species by subjecting them to a voltage gradient. A gel (made of agarose or polyacrylamide) provides mechanical support and prevents mixing of the molecules being separated. Electrophoresis performed in a gel matrix so that molecules of similar electric charge can be separated on the basis of size.

Gel retardation
A technique that identifies a DNA fragment that has a bound protein by virtue of its decreased mobility during gel electrophoresis.

Gel shift assay
Also known as gel retardation assay or gel mobility shift assay. See the definition under Gel retardation.

GFP
See Green Flourescent Protein.

Geminivirus
One of the two groups of DNA viruses that infect plants, the members of which have potential as cloning vectors for some species of higher plants.

Gene
The genetic unit of function. A gene may encode a polypeptide or a molecule of non-translated RNA (e.g. ribosomal RNA, transfer RNA, or a regulatory RNA).

Gene amplification
Multiple copies of a single gene within a cell.

Gene conversion
An genetic event that produces abnormal segregations by non-reciprocal recombination. Gene conversion has been extensively studied in ascomycetes, where it occurs following meiosis as the result of the formation of a mismatched base pair and subseque nt repair by the mismatch repair system.

Gene expression
The process by which a a gene product is produced. For genes that encode proteins, the gene must be transcribed into mRNA and then translated into protein. For genes that encode structural RNAs (rRNA, tRNA, etc), the gene must transcribed into RNA.

Gene fusion
A construct that joins the coding region of two open reading frames such that expression of the product results in a chimeric protein. For a more detailed description, see Operon and Gene fusions. Sometimes called a translational fusion or protein fusion.

Gene library
A random collection of DNA fragments (typically representing the entire genome of an organism) that have been inserted into a cloning vector.

Gene mapping
Determination of the relative positions of different genes on a DNA molecule.

Gene transfer agent
A phage-like agent from Rhodobacter capsulates species which can transfer DNA from the donor host to recipient cells.

Gene probe
A labelled sequence of single-stranded nucleic acid (DNA or RNA) which can be used to detect the complementary nucleic acid sequence by a hybridization techniques.

General (homologous) recombination
The common cellular mechanism for genetic recombination between DNA molecules with identical or near identical (homologous) nucleotide sequences. In enteric bacteria, homologous recombination requires the RecA protein.

Generalized transduction
The transfer of any region of the host chromosome into a recipient cell packaged in phage particles. Each phage particle only carries one region of the host chromosome, but within the population of phage every region of the host chromosome is represe nted. Generalized transduction usually results from an error resulting in packaging of host DNA into a phage particle. Typically such transducing particles only carry chromosomal DNA without any phage DNA.

Generation time
The amount of time required under specific exponential growth conditions for one cell to divide, forming two daughter cells.

Genetic code
The assignment of each of the triplet codons of mRNA to amino adds and translation stop signals. See Codon table.

Genetic engineering
The use of molecular techniques to produce DNA molecules containing new genes or new combinations of genes.

Genetic map
The relative position and distance between genes determined from recombination frequencies.

Genetic marker
A locus that has a useful phenotype which can be used for genetic selections or screens.

Genetic polymorphism
The existence of two or more genetically different classes within a population.

Genetic recombination
The process by which a fragment of DNA from one molecule (chromosome, plasmid, phage genome) is exchanged with or integrated into another molecule to produce a recombinant molecule(s).

Genome
The complete genetic content of a cell or organism, including chromosomes, plasmids, and prophages. The total genetic information of an organism. [The Oxford English Dictionary attributes the term genome to Hans Winkler who wrote in 1920 "I propose the expression Genom for the haploid chromosome set, which, together with the pertinent protoplasm, specifies the material foundations of the species ...." Source: J. Lederberg and A. McCray (2001) The Scientist 15:8]

Genomic library
A collection of clones that includes essentially all the genes of a particular organism.

Genomics
The comparative analysis of genomic DNA sequences from different organisms. Genomic analysis can provide information about the evolution of genes and can make predictions about the metabolism of an organism.

Genotype
A specific description of the genetic constitution of an organism. The genotype is defined by the allelic form of each gene in an organism, but for simplicity usually only differences from the wild-type are described.

Gentamicin
A type of aminoglycoside antibiotic. Often used to study bacterial entry into eukaryotic cells because gentamicin cannot cross the eukaryotic cell membrane, thus intracellular bacteria are resistant to gentamicin but extracellular bacteria are usually sensitive to gentamicin.

GMO
An abbreviation for “genetically modified organism”. Commonly used to refer to organisms that have been developed using recombinant DNA approaches, particularly if some foreign DNA remains in the strain.

Gradient of transfer
In an Hfr mating, the decrease in the inheritance of donor markers the farther they are from the origin of transfer.

Gram-negative bacteria
A group of bacteria with a cell wall composed of an outer membrane surrounding a thin peptidoglycan layer. When stained with crystal violet then treated with organic solvents, the dye is readily removed by the organic solvent.

Gram-positive bacteria
A group of bacteria with a cell wall composed of thick peptidoglycan layer and no outer membrane. When stained with crystal violet then treated with organic solvents, the dye is retained and thus the cells appear purple colored.

Green Flourescent Protein (GFP)
An intrinsically fluorescent protein from the jellyfish Aequorea victoria. Gene fusions with GFP are commonly used for determining protein localization by fluorescence microscopy.

Growth rate
The rate of increase of cellular density per unit time.
GUS
An abbreviation for Beta-glucuronidase (encoded by the uidA gene). Commonly used for constructing operon or gene fusions in organisms with high endogenous Beta-galactosidase activity. A variety of analogs exist that make it easy to detect GUS expression on solid medium and to assay the activity of the enzyme in cells.

Gyrase
See DNA gyrase.

Hairpin
A region of single-stranded DNA or RNA that can form base pairs between complementary sequences. For example the sequence 5′…GACGTGNNNNNCTGCAC…3′ could form a short double-stranded region between the sequences shown while any noncomplementary intervening sequences (shown as N to indicate any nucleotides) would form a single-stranded loop. Also called a “stem and loop” structure or a cruciform structure.

Half-site
The DNA sequence recognized by a dimeric protein is composed of two half-sites, with each half-site bound by a monomer. Half-sites are often inverted repeats, and more rarely direct repeats.

Hand-cuffing
A process that leads to replication inhibition in plasmids containing iterons. When a sufficiently high copy number of plasmid molecules accumulate, the replication initiator protein binds to the iteron sequences on two plasmids simultaneously, thereby inactivating both initiation of DNA replication of both plasmids.

Haploid
Only one copy of each chromosome per cell. (Prokaryotes are haploid, although more than one copy of a chromosome may be transiently present in the cell, depending on the rate of DNA replication and the growth rate.)

Headful packaging
The packaging (filling) of a viral capsid with viral nucleic acid until the capsid is full. Headful packaging is based upon the size of nucleic acid stuffed into the capsid rather than the recognition of specific sites on the viral genome. For an example, see the link on P22 packaging.

Heat shock response
A global regulatory response resulting in increased or decreased expression of a number of genes in response to injury by heat, osmotic change and certain other forms of stress.

Helper phage
A phage that is introduced into a host cell in to provide functions needed for replication, morphogenesis, or packaging of a mutant (defective) phage.

Helicases
Proteins that unwind the DNA double helix.

Hemimethylation
Double stranded DNA in which only one strand is methylated at a particular site. For example, at GATC sites in E. coli the A residues on both strands are methylated by DAM methylase but, because DAM methylase lags behind DNA polymerase, immediately after DNA replication only the parental strand is methylated.

Heteroduplex DNA
A double-stranded DNA molecule formed by annealing complementary (or partially complementary) single-stranded DNA from two different sources.

Heteroimmune phage
A phage that is not sensitive to the repression of lytic development by another prophage in the infected cell.

Heterokaryosis
The process whereby cells fuse to form a multinucleate cell containing nuclei from different parents. Nuclear fusion does not take place.

Heterologous
(i) DNA regions coding for the same function but with differences in their nucleotide sequences; (ii) DNAs which originate from different species.

Heterologous probe
The use of a labelled nucleic acid molecule to identify related molecules by hybridization probing.

Heterotrophic
The ability of an organism to use an organic molecule as carbon source.

Heterozygote
A diploid or partially diploid organism with different alleles of one or more particular genes.

Hfr (high frequency of recombination)
A cell in which the F-factor has integrated into a specific location in the chromosome, causing it to act as a highfrequency donor of chromosomal genes in crosses with F- cells.

HFT lysate
A lysate from a lysogenic phage that includes a substantial proportion of transducing fragments. For example, induction of a dilysogen that carries an insertion of both wild-type phage and a defective, specialized transducing phage will often yield about 50% transducing particles.

Histone
A basic protein from eukaryotes (or Archae) which binds to DNA, forming nucleosomes, and packaging the DNA into chromatin.

Histone-like proteins
Proteins from bacteria which bind to DNA, and compact the DNA.

Holin
A phage encoded lysis protein that forms pores (“holes”) in the cytoplasmic membrane and allows release of an enzyme that degrades peptidoglycan (e.g. lysozyme), facilitating lysis of the host cell.

Holliday junction
The cruciform structure formed as an intermediate in homologous genetic recombination.

Holoenzyme
A complex containing all of the subunits required for a functional enzyme. Used to describe enzymes composed of many different protein subunits. For example, RNA polymerase holoenzyme is composed of six subunits: 2 alpha subunits, beta, beta’, omega, and sigma.

Homoduplex
A molecule of double-stranded nucleic acid where the two strands have exactly complementary base sequences.

Homoimmune
Expression of a repressor by a lysogenic phage that prevents successful infection by another phage with the same repressor-operator recognition. For example, lambda lysogens are resistant to superinfection by another lambda phage because upon entering the lysogen, cI produced by the prophage turns off gene expression from PL and PR on the incoming phage.

Homologous
Nucleic acid molecules with the same base sequence except for minor differences in alleles; (ii) nucleic acid molecules originating from strains of the same species, thus having at least long stretches of identical DNA base sequences; (iii) gene or protein families having a recognizable common evolutionary origin.

Homologous recombination
The physical exchange of DNA between two homologous DNA molecules. Requires the RecA protein in enteric bacteria. Also called general recombination.

Homology
(i) Sequence identity between two nucleotide sequences. (ii) Genetic relatedness between two sequences of common ancestry. Commonly confused with sequence similarity. For example, 85% similarity means that 85 nucleotide positions out of 100 are identical in the two polynucleotides.

Homopolymer tailing
Attachment of a sequence of identical nucleotides (e.g. TTTTT) to the end of a nucleic acid molecule. Typically single-stranded homopolymer extensions are added to the ends of a double-stranded DNA molecule.

Homothallism
A process occurring in some yeasts and other fungal strains where haploid spores formed during meiosis undergo self-diploidization due to the switching of mating type by some of the progeny of the spore.

Homozygous
A cell or organism where the same allele is carried by each member of a pair of homologous chromosomes.

Horseradish peroxidase
An enzyme that can be complexed to DNA for use in some non-radioactive DNA labeling procedures.

Hostcontrolled restriction
A mechanism by which some bacteria degrade unmodified foreign DNA by a restriction endonuclease that recognizes a specific nucleotide sequence.

Host-range
The strain or species specificity of a bacteriophage, plasmid, or pathogen.

Hot spot
A region that is especially susceptible to mutations. Mutations occur at such sites at a much higher frequency than most other positions in the genome.

Hybridization probe
A labelled nucleic acid molecule that can be used to identify complementary or homologous molecules through the formation of stable base-paired hybrids.

Hybridization
A technique where a denatured (single-stranded) nucleotide chain (DNA or RNA) is allowed to pair with another single-stranded nucleotide chain. Hybridization will only occur if the two sequences are sufficiently related for a substantial number of hydrogen bonds to form between their complementary bases.

Hydroxylamine
NH2OH

– A mutagen that reacts with C residues, producing a modified base (N4-hydroxyC) that pairs with A instead of G, and hence resulting in GC to AT transition mutations.

Hydroxymethyl cytosine
A modification of cystine residues. This modification is typical of some phage DNA. The modified DNA is resistant to certain restriction endonucleases.

Hyphae
Multicellular filaments formed during the vegetative reproduction of fungi or actinomycetes.
Icosahedron
A regular geometric polyhedron with 20 equilateral trangular faces and 12 corners. This is a particularly stable structure. The capsid of many phages and viruses are icosahedral.

Illegitimate recombination
An aberrant recombination event between non-homologous sequences that occurs in the absence of a known site-specific recombination system.

Immunity
(i) The resistance of a lysogen to superinfection by a phage with a similar regulatory mechanism (also called homoimmunity). For example, expression of the cI repressor by a lambda prophage prevents expression of genes in a secondary infection if the cI protein can bind to the regulatory region of the superinfecting phage.
(ii) An adaptive antibody or cellular response against specific microbial infections.

Immunity region
The region of a lysogenic phage that encodes the major regulator of lysogeny and the cognate DNa binding sites (e.g. lambda cI protein and the leftward and rightward operator sites).

Immunological screening
The use of an antibody to detect a polypeptide encoded by a cloned gene.

Immunoassay
An immunological test to quantitate a particular protein using a antibody that binds specifically to the protein.

Incompatibility
The inability of two plasmids to stably coexist in the same cell.

Incompatibility group
A number of different types of plasmid, often related to each other, that are unable to stably coexist in the same cell.

Indel
A region of DNA that is present on the chromosome of an organism (Insertion) but absent from closely related organisms (Deletion).

Inducer
A chemical or physical agent that turns on gene expression. Usually refers to an agent that alters repressor-operator interactions, often by decreasing DNA-binding.

Inducible
A regulatory system where the genes are only expressed under appropriate conditions (e.g. when the substrate is present or in specific environmental conditions).

Induction
(i)The switching on of transcription in a repressed system due to the interaction between the inducer and a regulatory protein. For example, the lac operon is induced by adding lactose or IPTG.
(ii) Also used to describe a condition that causes a lysogen to begin lytic growth, as occurs when the cI repressor of phage lambda is inactivated following DNA damage.

Initiation factors
Proteins that promote the binding of ribosomes and the initiator tRNA to mRNA to begin the process of translation.

Inoculum
The initial sample of a microorganism added to a medium used to start a new culture.

Informational suppressor
A second mutation that restores function of a primary mutatioin by altering the way the gene is expressed. Examples of this class of suppressors include mutations that alter a tRNA allowing it to misread a nonsense (stop) codon or a frameshift mutation, or mutations in ribosomal genes that affect the fidelity of translation.

Insert
A fragment of DNA integrated into a cloning vector.

Insertion element (IS)
A transposable nucleotide sequence that only encodes the functions required for its own transposition. Insertion elements are typically less than 5 kb. Synonymous with “insertion sequence”.

Insertion sequence (IS)
A transposable nucleotide sequence that only encodes the functions required for its own transposition. Insertion sequences are typically less than 5 kb. Synonymous with “insertion element”.

Insertional inactivation
A cloning strategy where insertion of a piece of DNA into a vector inactivates a gene carried by the vector. Vector molecules with an insert can be identified by testing for the phenotype of this gene.

In situ
A Latin phrase meaning “in the original place”. Commonly used to describe a process that visualizes the position of a biological molecule in a cell.

In situ hybridization
A technique for gene mapping involving hybridization of a labelled sample of a cloned gene to a large DNA molecule (usually a chromosome), often within a cell.

Integron
DNA fragments that serve as sites for insertion of a variety of other DNA fragments (especially antibiotic resistance genes) and facilitate their transfer into other cells.

Intein
Selfish DNA elements located within coding regions that are translated with the interrupted protein, but then catalyze their own excision and the formation of a peptide bond between the flanking protein regions.

Interaction suppressor
A mutation at a second site that restores an interaction that was disrupted by a primary mutation. Interaction suppression can occur due to intragenic suppressor mutations (within the same gene that restore interactions of between domains of the protein) or intergenic suppressor mutations (mutations in two different genes that restore protein-protein interactions).

Intercalating agent
A planer molecule that can insert between two adjacent base pairs in a molecule of double-stranded DNA, distorting the architecture of the double helix. Intercalating agents often cause frameshift mutations. Examples include acridine orange and ICR191.

Intercalating dye
A dye which can insert between the bases of nucleic acids (e.g. ethidium bromide and acridine dyes. Intercalating dyes may be used to stain DNA or to induce frameshift mutation.

Intercalation
The insertion of flat polycyclic molecules between nucleotides in a DNA duplex. See Intercalating agent.

Intragenic complementation
The ability of two mutant forms of a gene, neither of which produce an active gene product, to produce a functional or partially functional gene product. Intragenic complementation is rare, typically only observed for specific missense alleles of a multimeric protein.

Intragenic suppressor
Restoration of partial or complete wild-type phenotype by second mutation in the same gene as a primary mutation which resulted in a negative phenotype. For example, a +1 frameshift mutation located a short distance downstream from a -1 frameshift mutation can restore the reading frame of a protein and thereby allow production of a functional product. Intragenic suppression can also occur via two missense mutations in a single reading frame.

Intramolecular
Within the same molecule. For example, intramolecular transposition is the movement of a transposon from one site on a DNA molecule to a different site on the same DNA molecule.

Intergenic suppressor
Restoration of partial or complete wild-type phenotype by second mutation in a different gene than a primary mutation which resulted in a negative phenotype. Intergenic suppression can occur in many ways, for example: A nonsense mutation that inactivates a gene may be suppressed by a second mutation that produces a nonsense suppressor tRNA. A mutation in a gene encoding a protein which must interact with a second protein may disrupt the interaction resulting in a negative phenotype; a compensating mutation in the gene encoding the second protein may restore the protein-protein interactions. Alternatively, the primary mutation may make a protein very sensitive to proteolysis, so there is a not sufficient amount of the protein available to fulfill its function; a mutation that inactivates a specific protease may allow accumulation of the first function, restorying the phenotype.

Intron
A sequence of a gene which is transcribed but which is excised by a splicing reaction before the mature mRNA is translated. Found in Eukarya, Archae, Bacteria, eukaryotic viruses, and phage. Introns are common in eukaryotes, but rarer in prokaryotes.

Inversion
A DNA rearrangement where a sequence of nucleotides is in the reverse orientation relative to the rest of the molecule.

Inverted repeats
A DNA or RNA sequence where the sequence of nucleotides along one a strand of DNA is repeated in the opposite physical direction along the other strand; inverted repeats are commonly separated by a tract of non-repeated DNA. For example:
3′ CTAG . . . GTAC 5′
5′ GATC . . . CATG 3′

In vitro
Reactions that take place outside of the cell; in a test tube.

In vitro mutagenesis
A method for mutating DNA outside of a host cell. Examples include, hydroxylamine mutagenesis of DNA packaged into phage particles or site-directed mutagenesis of plasmid DNA.

In vitro packaging
Synthesis of infective phage particles from a preparation of phage capsid proteins and a concatamer of phage DNA molecules. Commonly used to package DNA cloned onto a lambda vector (separated by cos sites) into infectious lambda particles.

In vivo
Reactions that take place inside the cell.

IPTG
An abbreviation for isopropyl-ß-D-thiogalactoside. A gratuitous inducer of the lac operon. That is, it can induce expression of the lac operon but it is not a substrate for the lac gene products.

IS element
An insertion sequence. A transposable element that only carries the genes required for its own replication. IS elements are usually less than 5 Kb. Also called an IS sequence.

Island
A large region of DNA that is present on the chromosome of an organism but absent from closely related organisms.

Islet
A smaller genetic island that only encodes one or a few gene products.

Isogenic
Two strains that are genetically identical except for a single mutation.

Iteron
Repetitive sequences in the origin region of some plasmids that are involved in the control of replication .
Join point.
The site where two DNA molecules are connected. Commonly used to describe the junction at the site of a DNA rearrangement such as an inversion mutation.

Junction fragments
DNA fragments adjacent to a particular region of DNA. For example, DNA sequences adjacent to a transposon insertion or DNA sequences adjacent to a DNA fragment that can be detected with a specific probe.

Junk DNA
Regions of DNA that do not encode functional proteins or RNAs and do not function as regulatory sites. Most eukaryotic genomes that have been characterized contain substantial amounts of junk DNA but most prokaryotic genomes that have been characterized contain less than 15% junk DNA. (However, there are exceptions — for example, the bacterium Mycobacterium leprae has substantial amounts of junk DNA.
Kanamycin (Kan)
An antibiotic that inhibits protein synthesis by binding to the 30s ribosomal subunit and preventing translocation. KanR is usually due to a cytoplasmic aminoglycoside phosphotransferase that inactivates kanamycin by covalently phosphorylating it. Because kanamycin rapidly inhibits protein synthesis, when cells acquire the kanR gene phenotypic expression is required before the cells become kanamycin resistant.

Kilobase (Kb or Kbp)
1000 nucleotides of DNA or RNA.

Kinase
An enzyme that transfers phosphate from ATP to another molecule.

Klenow fragment
A proteolytic fragment of DNA polymerase I that contains the DNA polymerase activity and the 3′ to 5′ proofreading activity but lacks the 5′ to 3′ exonuclease activity. This enzyme is widely used for DNA sequencing.
Labeling
The incorporation of a radioactive nucleotide into a nucleic acid molecule.

Lagging strand
The strand of newly replicated DNA that is synthesised discontinuously in the opposite direction from the replication fork. DNA synthesis proceeds in the 5′ to 3′ direction.

Lambda
A temperate phage that infects E. coli. Derivatives of phage lambda are widely used as cloning vectors.

Lambdoid
A group of phage that are related to the E. coli phage Lambda. Lambdoid phage share a similar gene organization and regulate the lysis-lysogeny decision in a similar way. Examples of lambdoid phage are the E. coli phage 434 and the Salmonella phage P22.

Latent period
The time between the initial infection of a cell with a virus and the production and release of new virions via lysis of the bacterial cell (contrast with eclipse period).

Leading strand
The strand of newly replicated DNA that is synthesised continuously in the same direction as the replication fork. DNA synthesis proceeds in the 5′ to 3′ direction.

Leaky mutation
A nucleotide substitution that changes the amino acid sequence of a protein that results in partial loss of its activity.

Ligase (DNA ligase)
An enzyme that repairs single-stranded discontinuities in double-stranded DNA molecules in the cell. Ligase joins a 3′-OH residue of a deoxyribonucleotide to the 5′-phosphate residue of an adjacent deoxyribonucleotide. Purified DNA ligase is used in gene cloning to join DNA molecules together.

Ligation
The formation of a phosphodiester bond between two adjacent bases separated by a single-strand break. Catalyzed by DNA ligase.

Linkage
The tendency of genes located close together on the same DNA molecule to be coinherited. Typically expressed as percent coinheritance of two genetic markers.

Linkage disruption
A genetic rearrangement or insertion that alters the coinheritance of otherwise linked genes.

Linkage map
A genetic map assembled from recombination data that shows the order of mutant sites and genes along a nucleic acid molecule.

Linked
Two genes located close together on the same DNA molecule that are coinherited at detectable frequency during recombination. See Linkage.

Linker
A synthetic, double-stranded oligonucleotide used to attach sticky ends to a blunt-ended molecule.

Locus (loci)
The position on a chromosome where a particular genetic trait resides. Sometimes used to describe multiple genes that affect the same function.

LPS
Lipopolysaccharide. A major componant of the outer layer of the outer membrane of Gram-negative bacteria.

Lysate
A solution containing progeny phage resulting from the lysis of a population of bacterial cells by infecting phage.

Lysis
Disruption of cells with release of the contents.

Lysogen
A bacterial cell carrying a phage genome as a repressed prophage.

Lysogenic cycle
The pattern of phage infection that involves integration of the phage DNA into the host chromosome.

Lysogenic conversion
Expression of particular genes by a prophage that confer a novel phenotype on the host (e.g. expression of a phage encoded toxin).

Lysogeny
The ability of a temperate bacteriophage to maintain itself as a quiescent prophage until induced into the lytic cycle.

Lysozyme
An enzyme that hydrolyzes the peptidoglycan within the cell walls of bacteria.

Lytic cycle
The development of a bacteriophage, either after infection of a host bacterium or after induction of a prophage, resulting in production and release of free progeny phage particles, and lysis of the host cell.

Lytic growth or lytic cycle
A phage infection where the phage replicates, matures, and ultimately lyses the bacterial cell, releasing free phage.

Lytic phage
A phage that can only enter the lytic cycle when it infects a sensitive bacterial cell.
M13
A filamentous, single-stranded DNA phage that infects E. coli. The M13 DNA replicates as a circular double-stranded intermediate (called a replicative form) then single-stranded DNA produced by rolling circle replication is packaged into phage particles. Derivatives of M13 are used as cloning vectors.

MacConkey plates
MacConkey medium contains pH indicators that can be used to differentiate colonies that can ferment a sugar from colonies unable to ferment a sugar. For example, on MacConkey-Lactose plates Lac+ colonies ferment lactose and the acid turns the pH indicator red colored, but Lac- colonies cannot ferment lactose so they remain white colored.

Male-specific phage
Phages that only adsorb to receptor sites on the F-pilus.

Map unit
An arbitrary unit representing the distance between genes, usually derived from the percentage of recombination, but also defined by the time at which the gene is transferred during conjugation.

Marker
A genetic trait of which one allelic form is selected or screened for following recombination.

Marker exchange
Use of recombination to switch allelic forms of a gene with a detectable phenotype. For example, to move a mutation from a plasmid or phage to the chromosome.

Marker rescue
Repair of a mutational defect by recombination. For example, when a cell is co-infected with a mutant phage that is unable to replicate and a wild-type phage, recombination between the two phage can repair the replication defect and allow the recombinant derivative of the mutant phage to reproduce.

Mating
See Conjugation.

Meiosis
The process of nuclear division associated with the formation of gametes or of haploid cells from a diploid.

Merodiploid
A partially diploid bacterium, carrying both its own chromosome and a chromosome fragment introduced by conjugation, transformation or transduction.

Messenger RNA (mRNA)
The transcript of a segment of chromosomal DNA which is a template for protein synthesis.

Methyl transferase
Enzymes that catalyze the transfer of methyl groups from one molecule to another.

Microarrays
Ordered sets of DNA fragments fixed to solid surfaces. The DNA fragments may represent all the open reading frames in a genome, a particular gene family, or any other subset of genes. Microarrays can be probed with RNA or cDNA derived from an organism to determine which transcripts are expressed under certain conditions. Microarrays are sometimes called gene chips.

Microinjection
A method of introducing new DNA into a cell by injecting it directly into the nucleus.

Minimal essential pairing sequence (MEPS)
The shortest length of DNA homology required for the initiation of homologous recombination.

Minimal medium
A defined medium that provides only the minimum number of different nutrients needed for growth of a particular bacterium.

Mismatch
A defect in the pairing of two complementary DNA sequences where a base in one strand is different from that expected according to complementarity with the other.

Mismatch repair
A mechanism that corrects mismatched base pairs that have escaped correction by the proofreading activities of the DNA polymerases.

Mispairing
Improper alignment of two nucleic acid strands.

Missense mutation
A mutation that changes a codon for one amino acid to a codon for a different amino acid, resulting in an amino acid substitution in the protein product.

Mitosis
The normal process of nuclear division in a eukaryote, whereby nuclear division occurs on a spindle structure without reduction in the chromosome number in the daughter nuclei.

Mobile element
A sequence of DNA that is able to promote its own transposition. An insertion sequence or a transposon.

Mobilizable plasmid
A plasmid that is not self-transmissible byt can be co-transferred with a self-transmissible plasmid, either independantly or as a cointegrate.

Modification (of DNA)
The specific addition of secondary residues (methyl, hydroxymethyl, glucosyl) to deoxyribonucleotides by an organism to differentiate its own DNA from other DNA or for regulatory purposes.

Monocistronic
An mRNA that only encodes a single gene product.

Mosaic
The substitution of portions of a gene with sequences acquired from another site or another organism via genetic recombination. Comparative sequence analysis indicates that many genes are composed of a “patchwork” of sequences derived from multiple recombination events.

Motif
A small portion of a protein (typically less than 20 amino acids) that is homologous to regions in other proteins that perform a similar function.

MOI
See Multipilicity Of Infection.

Moron
A short region of DNA that is inserted between a pair of genes in one phage genome but the genes of this same pair are adjacent in a related phage genome. The term (coined by Roger Hendrix) refers to the observation that one phage contains “more” DNA than the other phage at this particular spot. Many virulence factors of pathogenic bacteria are encoded in morons of integrated prophages.

mRNA
An RNA molecule that includes the coding region(s) and the translation signals for a gene or operon. An intermediate that specifies the amino acid sequence of the encoded polypeptide(s) during translation.

Mu
A bacteriophage that reproduces by transposition. Mu infects a variety of enteric bacteria.

Mud
A defective derivative of phage Mu. Mud insertions are commonly used to construct operon and gene fusions in enteric bacteria.

Multicopy plasmid
A plasmid with a high copy number.

Multifactorial
A phenotype caused by two or more genes.

Multigene family
A number of identical or related genes present in the same organism, usually coding for a family of related polypeptides.

Multiplicity of infection (MOI)
The ratio of pathogen to host cells during an infection. For example, the ratio of phage P22 to Salmonella cells, or the ratio of Salmonella to cultured macrophages.

Mutagen
A chemical or physical agent that increases the frequency of mutation, usually by directly damaging the DNA.

Mutagenesis
The formation of mutations.

Mutant
An organism with an altered base sequence in one or several genes. Usually refers to an organism with a mutation that causes a phenotypic difference from the wild-type.

Mutation
Any heritable alteration in the base sequence of the genetic material. See Types of mutations

Mutation rate
The number of mutations per cell division. The mutation rate can be determined from a Luria-Dulbruck fluctuation analysis. Sometimes the mutant frequency is described instead of mutation rate. The mutant frequency is simply the ratio of mutants / total cells in the population. The mutant frequency is much easier to measure but may show large fluctuations depending upon when the first mutation appeared in the population.

Mutator gene
A mutant gene which increases the frequency of mutation in other genes. Mutations in genes responsible for DNA repair typically have a mutator phenotype. For example, mutations in the genes responsible for methyl-directed mismatch repair, designated mutS, mutL, and mutH, increase the spontaneous mutation frequency about 1000-fold. See Mutator strains.
Nalidixic acid
An antibiotic that inhibits DNA gyrase.

Negative dominance
A gene product that inhibits the function of another gene product.

Negative regulation
A mechanism of genetic regulation in which a protein or RNA molecule inhibits gene expression, e.g. by preventing the transcription of a gene or translation of the mRNA. A negative regulator that inhibits transcription of a gene is commonly called a repressor.

N-glycosylases
Repair enzymes that are able to excise certain incorrectly paired or damaged nucleotides.

Nick
A single-strand break, involving the absence of one or more nucleotides, in a double-stranded DNA molecule. A break in the phosphodiester bond between adjacent nucleotides in one strand of a DNA duplex.

Nick translation
A method which uses DNA polymerase I to first produce a nick in a DNA duplex, then degrade stretch of single-stranded DNA using its 5′-exonuclease while synthesizing a new strand in its place. By including a labeled dNTP in the reaction, the newly synthesized DNA will be labeled.

Non-composite transposon
A transposible element that is NO
O-antigen
The arrangement of polysaccharide side chains on the LPS of Gram-negative bacteria. Serves as the receptor for some types of phage.

Ochre codon
The UAA stop codon.

Ochre mutation
A change in a codon to create the nonsense codon UAA (the ochre codon).

Okasaki fragments
Short DNA fragments of about 1000-2000 nucleotides long formed during DNA replication of the lagging strand by discontinuous replication of DNA. Okasaki fragments are later joined together by ligation.

Oligonucleotide
A short sequence of polynucleotide. Oligonucleotides with a defined sequence can synthesized in vitro for use for a variety of techniques, including PCR, DNA sequence analysis, hybridization, and site-directed mutagenesis. The length of an oligonucleotide is described as a #-mer — for example, an oligonucleotide with 20 nucleotides would be called a 20-mer).

Oligonucleotide-directed mutagenesis
An in vitro mutagenesis technique that involves the use of a synthetic oligonucleotide to introduce the predetermined nucleotide alteration into the gene to be mutated.

-ome
This suffix indicates the complete collection of the subunits described in the word stem. For example, genome indicates the entire haploid complement of genetic material in an organism, pproteome indicates the entire set of proteins expressed by an organism, etc. [Source: J. Lederberg and A. McCray (2001) The Scientist 15:8]

One-step growth curve
A plot of the production of lytic growth of a virus vs time. An excess of bacteria is infected with virus. There is an initial drop in the number of plaque forming units (PFU) of virus due to entry of the virus into cells and release of the viral nucleic acid. This is followed by a period of time called the eclipse phase where viral proteins and nucleic acid are reproduced but no viable virus is produced. After this period mature viruses are assembled and released from the cell. The “burst size” is the number of virus particles released from the cell divided by the number of virus particles initially added. The one-step growth curve is terminated after the first round of infection.

Opal codon
The UGA stop codon.

Opal mutation
A change in a codon to create the nonsense codon UGA (the opal codon).

Open reading frame (ORF)
A stretch of DNA which potentially codes for protein. A length of DNA not interrupted by stop codons. A sequence of in frame codons preceded by a translational initiation codon and terminated by a chain termination triplet.

Open-circular
The non-supercoiled conformation taken up by a circular double-stranded DNA molecule when one or both polynucleotides carry nicks.

Operator
The DNA sequence where a repressor protein reversibly binds to regulate the activity of one or more closely linked structural genes.

Operon
A sequence of adjacent genes read as a single, polycistronic mRNA. Changes in the level of transcription thus affects all of the genes in an operon, so such genes are often coordinately regulated. Includes both the structural genes, and the operator and promoter sequences that control them.

Operon fusion
A construct that places the coding region of a gene downstream of the promoter for another gene, such that transcription of the downstream gene initiates from this new promoter but translation of the downstream gene occurs from its own translation start site. For a more detailed description, see Operon and Gene fusions. Sometimes called a transcriptional fusion or fusion.

Origin of replication (ori)
The nucleotide sequence where DNA replication is initiated. Determines the specific position on a DNA molecule where DNA replication begins.

Orthogonal field alternating gel electrophoresis (OFAGE)
A gel electrophoresis technique that employs a pulsed electric field to achieve separation of very large molecules of DNA.

Orthologous
A gene present in multiple species that descended from a unique ancestral gene, when the relative divergence in different species is comparable to the overall difference between the species. Such genes provide useful tools for constructing phylogenetic trees (for examples, see http://www.ncbi.nlm.nih.gov/COG/).

Outer membrane
The lipopolysaccharide (LPS) containing layer, containing some proteins, which surrounds the cytoplasmic membrane and forms the outermost layer of most Gram-negative bacteria. The outer membrane usually confers resistance to many detergents and contains the receptor sites for certain phage.

Overlapping genes
Two genes whose nucleotide sequences partially overlap. The two genes may be translated in different reading frames with the 3′ end of one structural gene overlaping with the 5′ end of another structural gene, the two genes may be translated in different reading frames with one structural gene located entirely within the other, or the two genes may be translated in the same reading frame with one structural gene located entirely within the other.

Overproduction suppression
Suppression of a mutant phenotype by expression of a protein at high levels due to a regulatory mutation or expression from a multicopy plasmid. Typically overexpression suppression is used to describe the partial or full restoration of the wild-type phenotype by high levels of a protein with weak activity, either the corresponding leaky mutant protein or another gene product with weak activity.
PAGE
Polyacrylamide gel electrophoresis. Separation of molecules through a polyacrylamide gel matrix in an electric field. Separation may depend upon size and charge of the molecules.

Palindrome
A sequence of DNA that reads the same in the 5′ to 3′ direction on the complementary strands. For example -
5′ GATC 3′
3′ CTAG 5′

Often described as inverted repeats or sequences with dyad symmetry. Many DNA-binding proteins recognize palindromic sequences. Note that the grammatical usage of this term is differnet than the way it is used in genetics and molecular biology – in gramme r it is used to describe a word string that reads the same if read from right to left as if read from left to right.

Papillae
Small colonies that appear within or at the edge of a colony. For example, blue Lac+ papillae may occur in a white Lac- colony on X-gal plates. (For an excellent example of a papillation assay, see Nghiem et al. 1988. Proc. Natl. Acad. Sci. USA 85: 2709-2713.)

Paralogous
Genes that descended from an original copy of the gene that duplicated within an ancestral genome, and thus each copy of the gene could diverge independently. Because paralogous genes can vary within a species as much as between species, such genes are useful tools for studying protein evolution but not for constructing phylogenetic trees.

Partial digestion
Treatment of a DNA molecule with a restriction endonuclease under such conditions that only a fraction of all the recognition sites are cleaved. Commonly used to produce a random collection of DNA fragments for construction of gene libraries.

Partitioning
Separation of chromosomes or plasmids into daughter cells following DNA replication and cell division.

Pathogenecity island (PAI)
A region of a bacterial chromosome that seems to have been acquired via horizontal gene transfer and includes a group of genes encoding virulence factors. Evidence of horizontal gene transfer may be comparison with genomes from related nonpathogenic bacteria, or by flanking genes that suggest transfer via phage, conjugation, or transpositiion. The GC content and codon usage of PAI is often different from the rest of the chromosome.

PCR
Polymerase chain reaction. A method for amplifying a particular region of DNA by a sequence of denaturation, annealing of specific primers, and synthesis. Use of a thermostable DNA polymerase (such as Taq polymerase) allows the reactions to be perfo rmed in a thermocycler that automatically adjusts the temperature to the optimal for each reaction through many cycles. The concentration of the amplified DNA fragment increases exponentially with each cycle.

Penicillin (Pen)
An antibiotic that inhibits crosslinking of peptidoglycan chains in the cell wall of bacteria. Cells growing in the presence of penicillin synthesize weak cell walls, causing them to burst due to the high internal osmotic pressure. PenR usually results from expression of periplasmic ß-lactamase that breaks the Beta-lactam ring of the antibiotic. A large variety of penicillin derivatives are available. Ampicillin is a commonly used derivative of penicillin.

Peptidoglycan
The structural component of most bacterial cell walls.

Permease
An enzyme system concerned with the transport of specific substances, usually nutrients, through the cytoplasm membrane.

Permissive conditions
A particular environmental condition which allows the growth of an organism with a conditional mutation. For example, for temperature sensitive mutations 30 C is typically a permissive temperature and 42 C is the nonpermissive condition.

PFGE
See Pulsed field gel electrophoresis.

PFU
Abbreviation for plaque forming unit.

Phage (also called Bacteriophage)
A bacterial virus.

Phage head
The capsid which contains the phage nucleic acid. Often used to describe icosahedral capsid. The pressure inside an icosahedral head from a typical dsDNA phage is about 60 ATM.

Phagemid
A plasmid that contains a portion of a phage genome. Upon co-infection of the host with a Helper phage, the plasmid can be packaged into phage particles. A commonly used type of phagemid is packaged as ssDNA into phage M13 particles.

Phage induction
A treatment which stimulates prophage to enter; the lytic cycle; eventually the host cell lyses and releases free phage.

Phage tail
Proteins that extend from a phage head and mediate adsorption to receptors on the host cell.

Phase variation
A mechanism which results in variable expression of surface antigens. An example is the switch between H1 and H2 flagellar antigens by an invertable switch in Salmonella.

Phenocopy
An environmental condition that results in a phenotype different that that usually observed for a certain mutant. For example, the surfact properties of F+ bacteria can be altered to mimic F- bacteria when grown to stationary phase in medium with glucose as a carbon source.

Phenol extraction
A method commonly used to remove proteins from aqueous DNA samples. Phenol denatures proteins. The denatured proteins partition into the organic phase or remain at the interphase but the DNA remains in the aqueous phase.

Phenotype
The appearance or other observable characteristics of an organism. The phenotype expressed by an organism depends upon the particular forms of its genes (e.g. its wild-type or mutant alleles) and the environmental conditions.

phoA
The gene encoding alkaline phosphatase. Alkaline phosphatase is inactive unless it is exported outside of the cytoplasm where it becomes oxidized. Thus, gene fusions to phoA are commonly used to identify protein domains that are translocated outside of the cytoplasm (including cytoplasmic membrane protein domains exposed to the periplasm, periplasmic proteins, outer membrane proteins, or excreted proteins).

Phosphodiester bond
The covalent bond joining the 3′ hydroxyl of the sugar moiety of one (deoxy)ribonucleotide to the 5′ hydroxyl of the adjacent sugar.

Photoreactivation
The repair of ultraviolet irradiated DNA by the cleavage of pyrimidine dimers. Catalyzed by the photoreactivating enzyme, an enzyme that requires post-irradiation exposure to visible light.

Phylogeny
The classification of organisms according to evolutionary criteria.

Physical map
The linear order of genes and distance between them (usually expressed in base pairs or kilobases). Physical maps are constructed from in vitro characterization of the DNA (e.g. by restriction mapping or DNA sequencing).

Physiological suppression
A second mutation that affects an aspect of cell physiology and thereby restores the function of a primary mutation. For example, a mutation in a protease may allow accumulation of a partially active mutant protein, thereby restoring sufficient function to repair the mutant phenotype; a second mutation that increases accumulation of a limiting substrate may restore function of a primary mutant that has poorer substrate binding; a mutation that increases proline accumulation may suppress a primary mutant with a protein folding defect; etc.

Pilus
A filamentous protein polymer protruding from the cell surface. Usually involved in attachment to other cells or surfaces. For example, the F-pilus expressed in E. coli cells that carry the F-plasmid is involved in attachment to F- cells prior to conjugation. The plural of pilus is pili.

Plaque
A clear area in a lawn of bacterial cells caused by the lysis of infected cells by a phage.

Plaque forming unit
A virus particle capable of forming a plaque, indicating that it is able to infect, reproduce, and kill host cells.

Plasmid
A molecule of extrachromosomal DNA existing as an autonomous replicon in the cytoplasm. Most plasmids are covalently closed circular (CCC) DNA, although examples of linear plasmids are known.

Pleiotropic
A single mutation that simultaneously changes several apparently unrelated phenotypes.

Point mutation
A mutation involving the substitution, addition, or deletion of a single base pair .

Poisson distribution
A statistical test developed by Simeon Poisson . The Poisson equation describes the probability distribution of random events — for example, the probability that random mutations in a cell will affect a particular gene, or the average number of viruses to infect a single cell at a particular multiplicity of infection.

Polar mutation
A mutation which affects not only the gene in which it is located but other genes located immediately downstream on the DNA molecule. See Rho dependent polarity .

Polyacrylamide gel electrophoresis
See PAGE.

Polycistronic
An mRNA that encodes several discrete gene products.

Polylinker
A short, synthetic DNA sequence containing several restriction enzyme recognition sites. Polylinkers facilitate cloning into plasmid or phage vectors.

Polymerase chain reaction
See PCR.

Polysome
An mRNA molecule that is in the process of being translated by multiple ribosomes simultaneously.

Polytopic
Commonly used to describe membrane proteins that span the membrane multiple times, such that different regions of the protein are exposed on opposite sides of the membrane. (“Topic” refers to the topology of the protein in the membrane.)

Positive supercoiling
Additional coiling of the circular duplex DNA molecule in the same direction as the winding of the double helix.

Post-meiotic segregation
The type of segregation produced when a recombinant DNA molecule contains an uncorrected mismatched base pair; at the next replication, normal base pairing occurs producing one mutant progeny and one wild-type progeny.

Post-replication repair
A DNA repair process which occurs after DNA replication.

Post-replication repair
A DNA repair process which occurs after DNA replication.

Post-transcriptional regulation
Regulation of gene expression after the gene has been transcribed into mRNA. For example, by regulation of translation, regulation of protein activity, or regulation of protein turnover.

Post-translational modification
The modification of proteins after the protein has been synthesized. Proteins may be modified in a wide variety of ways, including phosphorylation (addition or a phosphate group), adenylation (addition of an adenine group), glycosylation (addition of a sugar group), acylation (addition of a lipid group), proteolysis (removal of the initiator methionine, cleavage of a signal sequence, or cleavage of a pro-peptide), etc. are subject to a multitude of modification steps. These modifications can have profound, sometimes reversible effects on protein structure and function.

Post-translational regulation
Regulation of gene expression after the gene has been transcribed into mRNA and translated into protein. For example, by regulation of protein activity by covalent modification or proteolysis.

Primase
An enzyme that synthesizes ribonucleotide primers for lagging strand DNA synthesis of Okazaki fragments. Polymerizes ribonucleotide triphosphates in the 5′ to 3′ direction.

Primer
A short oligonucleotide complementary to a strand of DNA or RNA that is used to initiate synthesis of the complementary DNA strand. The primer provides a 3′OH end which is required by DNA polymerases to initiate synthesis of the complementary DNA.

Primosome
A complex of primase and helicase that initiates synthesis of RNA primers on the lagging DNA strand during DNA replication.

Probe
A fragment of DNA labeled with radioactivity or chemiluminescence and used to hybridize to another DNA molecule to identify complementary base sequences.

Procaryote
An organism lacking a nuclear membrane and certain organelles such as mitochondria. Refers to both Bacteria and Archae. This term was used synonymously with bacteria before the differences between Bacteria and Archae were understood. Although prokaryotes share some common features because of the lack of membrane bound organelles (e.g., coupled transcription and translation are possible in prokaryotes but not in eukaryotes), overall the Archae are more similar to the Eukarya than they are to Bacteria.

Processivity
The ability of an enzyme to continue to act on a polynucleotide for a long distance without dissociating.

Promiscuous plasmid
A plasmid with a broad host-range.

Promoter
A sequence on DNA that functions as the RNA polymerase binding site, thus defining the transcription start site. Promoter recognition is largely determined by the sigma factor associated with RNA polymerase and the interaction of RNA polymerase with positive regulatory proteins. The consensus sequence for a promoter depends upon the sigma factor associated with RNA polymerase.

Prophage
A temperate phage genome whose lytic functions are repressed and which replicates in synchrony with the bacterial chromosome. A prophage may be integrated into the host chromosome (as with phage lambda) or exist as an autonomously replicating plasmid (as with phage P1).

Proflavin
An intercalating agent used as a frameshift mutagen.

Proofreading
Removal of mismatched base pairs during DNA replication by the 3′ to 5′ exonuclease activity of DNA polymerase, followed by resynthesis.

Protease
An enzyme that degrades proteins to peptides or amino acids.

Proteolysis
The degradation of proteins to peptides or amino acids catalyzed by proteases.

Proteomics
The large-scale study of proteins, using biochemical or physical methods. Approaches include two-dimensional electrophoresis of proteins expressed under particular conditions or in particular cell compartments, Mass spectometry of proteins, use of hybrid approaches to identify protein-protein interactions, large scale crystallography of cellular proteins, etc. This approach complements the analysis of genome sequences (genomics) because it identifies the protein gene products that perform the cellular functions encoded by genes; The analysis of all (or most) of the proteins encoded by a genome. Some of the techniques used to characterize the proteins on this scale include bioinformatics, 2-dimensional gel electrophoresis, mass spectrometry, and protein microarrays.

Prototroph
A microorganism that is able to grow on minimal medium containing only a carbon source and inorganic salts.

Pseudogene
An inactive gene derived from an ancestral active gene. Pseudogenes are often recognized by nonsense or frameshift mutations that disrupt an open reading frame that encodes a functional protein in a related genome.

Pseudoreversion
Reversion of a mutant phenotype caused by a second mutation at a different site that partially or fully restores the wild-type phenotype. See suppression.

Pseudorevertant
A revertant that retains the original mutation but has a second mutation at a different site that partially or fully restores the wild-type phenotype. See suppressor.

Pulsed field gel electrophoresis
A gel electrophoresis technique that employs an electric field that alternates between two different vectors to achieve separation of very large molecules of DNA.

Puromycin
An antibiotic that inhibits protein synthesis. Puromycin is an analog of charged tRNA that binds to the ribosome, and is transferred to the growing peptide chain. The polypeptide is released from the ribosome resulting in premature translation termination. Puromycin inhibits protein synthesis in Bacteria, Eukarya, and Archae.

Pyrimidine dimers
Covalent bonds formed between two adjacent pyrimidines on the same strand of DNA induced by Ultraviolet irradiation.
Quarternary structure
The folded structure of a protein including all of the polypeptides required for the intact, fuctional protein.

Quiescent
Silent or inactive.

Quinolones
A group of antibiotics that inhibit DNA gyrase. For example, nalidixic acid.
Radioactive suicide
The death of cells due to incorporation of a radioactive substrate with high specific activity. Radioactive suicide can be used as a technique to select for mutants that are unable to incorporate a particular substrate.

Random primers
A set of short oligonucleotides with variable sequences. Within a population of random oligonucleotides, some will anneal to complementary sequences in a DNA or RNA template. Use of random primers to initiate DNA synthesis in the presence of a radiol abeled (or chemiluminescent) dexoynucleotide (dNTP) will yield probes representing the sequences found in the template DNA. The labeled probes can then be used to identify other sequences homologous to this DNA (e.g. by Southern blotting).

Read-through
Failure to stop transcription at a normal termination signal.

Reading frame
The sequence of nucleotides which is read as consecutive triplets during translation of mRNA into protein. A sequence of codons that continues without encountering a stop codon is called an open reading frame (ORF). For a sequence of double-stranded DNA there are six possible reading frames; three in the forward direction, and three in the reverse direction. A sequence of DNA will often have one ORF, but in some cases a sequence of DNA will include overlapping ORFs that encode distinct polypeptides.

Reciprocal crosses
Pairs of genetic crosses which in one case DNA from strain #1 is transferred into strain #2 and in the second case the strain #2 is used as a donor to transfer the same region into strain #1. For example

Cross A = donor (pro::Tn10) x recipient (pro+)

Cross B = donor (pro+) x recipient (pro::Tn10)

Reciprocal recombination
A precise exchange of genetic information like that expected for a simple cut, exchange, and rejoin mechanism. That is, a region of DNA simply moves from the donor molecule to the recipient molecule in exchange for the identical region from the recipient molecule.

RecA protein
The protein encoded by the recA gene which is essential for homologous recombination. The RecA protein is also involved in the induction of the SOS response and the induction of lambda prophage in response to DNA damaging agents.

Recessive
A genetic trait that is not expressed in a heterozygous or partially heterozygous cell.

Recombinant DNA
A molecule of DNA in which a DNA fragment from a different source has been inserted.

Recombinase
An enzyme that catalyzes genetic recombination.

Recombination
Genetic exchange resulting from a cross-over between two different DNA molecules or different regions of a DNA molecule. See General recombination, Illegitimate recombination and Sitespecific recombination.

Recombination frequency
The number of recombinants divided by the total number of progeny. The recombination frequency is proportional to the physical distance between two genetic markers, and thus recombination frequencies can be used to draw genetic maps showing the relat ive distance between genetic markers. Note that often the coinheritance frequency — the probablity that recombination did NOT occur between two markers is used instead of the recombination frequency.

Recombineering (“Recombination-mediated genetic engineering”)
A term coined by Don Court to describe a method for vector construction based on homologous recombination in E. coli using lambda phage recombination proteins exo, bet, and gam. This process allows homologous recombination between much shorter DNA sequences than the E. coli homologous recombination system. See http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/in-vitro-genetics/red-swap.html.

Redundant genes
Multiple copies of a gene or different genes with the same function.

Regulon
A group of genes or operons located at different positions on the chromosome but respond to a common regulatory protein.

Release factors (RF)
Proteins that facilitate the termination of translation. Translation termination occurs when a ribosome encounters one of the three stop codons (UAA, UAG, or UGA). These codons are not recognized by a tRNA but by protein release factors. RF-1 recognizes UAA and UAG, RF-2 recognizes UAA and UGA. RF-3 stimulates the activity of RF-1 and RF-2. Interaction of the RF with a stop codon causes the peptidyl transferase activity of the ribosome to catalyze the hydrolysis of the ester bond between the tRNA and the polypeptide chain, releasing the polypeptide chain and resulting in dissociation of the ribosome.

Replica plating
A technique for transferring an identical pattern of bacterial colonies from one petrie plate (the master plate) to a series of other plates containing different media. A plate containing bacterial colonies is pressed against a cylindrical block covered with velveteen, resulting in the transfer of many of the bacteria from each colony onto the corresponding position on the velveteen. Then a series of sterile plates are sequentially pressed against the velveteen to transfer cells from the velveteen to the corresponding position on each petrie plate. After incubation, if the cells can grow on the particular medium in a plate colonies will appear at identical positions on each plate. Typically about 10 replica plates can be made from each master plate with about 200 isolated colonies on the master plate. Thus, it is possible to quickly screen a large number of colonies for a variety of phenotypic characteristics.

Replication
The process of duplicating a DNA molecule.

Replication fork
The region on a replicating doublestranded DNA molecule where synthesis of new DNA is taking place. The replicating fork produces a Yshaped region in the DNA molecule where the two strands have separated and replication is taking place.

Replication restart
An event that occurs when replication forks that collapse or disintegrate spontaneously do not progress to the completion of the chromosome; the replication fork is reasembled at the site of its collapse.

Replicative transposition
The insertion of a transposable element at a new location without loss from the original location.

Replicon
A DNA molecule that is able to initiate its own replication. A replicon must have an origin of replication and usually also has the necessary regulatory information required for the proper initiation of DNA replication.

Replicon fusion
The integration of one replicon into another to form a single replicon. May occur by recombination between homologous regions of two replicons or by formation of a cointegrate during transposition of a transposable element located on one of the repli cons.

Reporter gene
A gene which can be placed downstream of a promoter and expression of the gene followed by a relatively easy assay (often a colorimetric assay). See operon and gene fusions.

Repression
Switching off the expression of a gene or a group of genes in response to a chemical or other stimulus.

Repressor
A gene product that negatively regulates gene expression. Usually refers to a DNA-binding protein that inhibits transcription under certain conditions. Transcriptional repressors typically decrease the transcription of certain other genes by specifically binding to operator sites — one or more short DNA sequences located upstream of the structural gene. Regulation of repression is usually modulated by a ligand which binds to the repressor protein and alters its DNA-binding properties. DNA-binding may be increased by association with a co-repressor or DNA-binding may be decreased by association with an inducer.

Resistance transfer factor (RTF)
The component of an R-plasmid that encodes the ability to conjugate and to transfer DNA.

Resolvase
An enzyme which resolves a co-integrate molecule into its two component replicons.

Response regulator
A regulatory protein that responds to sensor protein of a “two-component” regulatory system. Interaction with the transmitter domain of the sensor protein, leads to the phosphorylation or dephosphorylation of an aspartate residue on the response regulator. The modified protein regulates gene expression in response to the changes in the environment.

Restriction
The cleavage of double-stranded DNA by an endonuclease (restriction enzyme). The restriction enzyme distinguishes between self and foreign DNA based upon the modification of its DNA-binding site (for example, by methylation).

Restriction analysis
Determination of the number and sizes of the DNA fragments produced when a particular DNA molecule is cut with a particular restriction endonuclease.

Restriction endonuclease
An endonuclease cuts doublestranded DNA by binding to specific sites, in many cases arranged in palindromes. Several different classes of restriction endonucleases can be differentiated based upon their binding and cleavage sites and their required cofactors. Although restriction endonucleases have specific recognition sites, cleavage may occur at specific or random sites depending on the class of the endonuclease. Also called restriction enzymes.

Restriction fragment length polymorphism (RFLP)
A mutation that results in a detectable change in the pattern of fragments obtained when a DNA molecule is cut with a restriction endonuclease.

Restriction map
A map showing the positions of different restriction sites in a DNA molecule.

Restriction-modification
The modification of host DNA to prevent cutting by a restriction endonuclease (see restriction endonuclease). The modification is often via methylation of a specific restriction site sequence.

Restriction site
A DNA sequence recognized and cleaved by a restriction endonuclease. Restriction sites are often 4 to 6 bp, but some sites are 8 bp or longer. The presence or absence of specific nucleotide modifications (e.g. methylation) determines whether the restriction endonuclease cleaves at its cognate restriction site.

Restrictive conditions
The particular environmental conditions which do not allow growth of a conditional lethal mutant but result in the expression of the mutant phenotype.

Retroregulation
The effect of a downstream RNA sequence upon the expression of an upstream sequence. First used to describe the regulation of the phage lambda xis gene (see http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/phage/int-xis.html)

Retrotransposon
A genetic element that transposes to a new location in DNA by first making an RNA copy of itself, then making a DNA copy of this RNA with a reverse transcriptase, and then inserting the DNA copy into the target DNA.

Reverse genetics
An approach where a cloned gene with an unknown function is used to disrupt the corresponding chromosomal gene to examine the resulting phenotype.

Reverse transcriptase
An enzyme produced by retroviruses that can synthesize a strand of DNA complimentary to an RNA template. (Reverse transcriptase can also synthesize DNA from a DNA template.) Used to make cDNA clones from mRNA.

Reversion
Any mutation that restores the wild-type phenotype of a mutant.

R-factor
A transmissible plasmid that carries genes coding for resistance to several different antibiotics. Also called R-plasmid.

RFLP
See Restriction fragment length polymorphism.

Rho factor
A protein which catalyzes transcription termination at certain sites or when an extended stretch on nontranslated, unstructured RNA is present. See Rho dependent polarity .

Ribosomal (rRNA)
An RNA molecule that forms part of the structure of a ribosome.

Ribosome
An RNA-protein complex responsible for the correct positioning of mRNA and charged tRNAs allowing proper alignment of amino acids during protein synthesis.

Ribosome binding site
A short nucleotide sequence upstream of a gene which forms the site on the mRNA molecule where the ribosome binds. (Also called a Shine-Delgarno sequence.)

Rich medium
A growth medium in which not all the components have been identified. Most “rich” media have a variety of complex, undefined componants.

rII locus
A region from phage T4 that determines whether this phage can grow on E. coli K or B strains. Fine structure genetic mapping of the rII locus by Sydney Benzer first unveiled a variety of important facets of gene structure and function.

RNA phage
A phage that carries RNA as its genetic material. Some examples include phage MS2 and Qß.

RNA polymerase (RNAP)
An enzyme complex that polymerizes RNA from ribonucleotides (NTPs), using one strand of DNA as template (hence called “DNA-dependent RNA polymerase). The core RNAP from E. coli is composed of five subunits: 2 alpha subunits, beta, beta’, and omega. Upon binding another subunit called sigma, RNAP is called a holoenzyme. The sigma subunit (or sigma factor) reduces the nonspecific affinity of RNAP for DNA and increases the specific binding to certain promoter sequences. A variety of different sigma subunits exist, each promoting RNAP binding to different promoters under specific physiological conditions.

Rolling circle (sigma) replication
A type of DNA replication where a replication fork moves around a circular DNA molecule, producing a single-stranded concatamer (much like the way toilet paper peels off the roll). The resulting single-stranded DNA may become double-stranded by the synthesis of a complementary strand.

RNase
An enzyme that hydrolyses RNA molecules.

RPM
Revolutions per minute. Often used to describe the velocity of a centrifuge.
Same-sense mutation
A mutation which changes the nucleotide sequence of a codon but does not change the amino acid encoded due to the degeneracy of the genetic code. For example, both CCC and CCA encode proline.

Sanger sequencing
A method used to determine a DNA sequence based upon the incorporation of dideoxynucleotides.

Scaffolding proteins
Proteins which facilitate the assembly of a cell structure but are not included in the final structure. For example, phage encoded proteins that are required for procapsid assembly but are removed after the procapsid is constructed.

Score
To determine the presence or absence of a phenotype by testing for growth under different conditions (e.g., plus and minus an auxotrophic supplement or permissive and nonpermissive conditions). Usually done by replica plating or patching colonies onto each type of plate. Synonymous with “screen”.

Screen
To determine the presence or absence of a phenotype by testing for growth under different conditions (e.g., plus and minus an auxotrophic supplement or permissive and nonpermissive conditions). Usually done by replica plating or patching colonies onto each type of plate. Synonymous with “score”.

Secreted protein
A protein that is exported through the cytoplasmic membrane. Most secreted proteins have specific signal sequences that promote interaction with the export apparatus in the membrane.

Segregrate
See segregration below.

Segregration
The loss of one allele during cell division. For example, one allele maybe lost from because it fails to replicate or partition into one of the daughter cells.

Selectable marker
A mutation that confers a phenotype on a cell such that when grown on a certain medium only those cells with the mutation will grow. For example, the mutation rpsL1 makes cells resistant to the antibiotic streptomycin — when grown on medium with streptomycin rpsL1 mutants will grow but rpsL+ cells will die.

Selected marker
An allele that allows growth under a particular selective condition.

Selective media
Growth media that only allow growth of mutant or recombinant cells with a particular phenotype grow. For example, media containing tetracycline would select for tetracycline resistant bacteria, preventing growth of parental tetracycline sensitive bacteria.

Selection
Conditions where only mutant or recombinant cells with a particular phenotype grow and divide.

SELEX
A method for isolation of high-affinity RNA- or DNA-protein interactions through successive rounds of selection for increased nucleic acid binding.

Selfish DNA
A DNA sequence that does not contribute to the fitness of an organism but is maintained in the genome because it promotes its own replication.

Serovars
Different strains of the same species of bacterium that can be distinguished by different reactions to certain antibodies (anti-sera). The name derives from the terms SEROlogical VARiety.

Sense strand
The strand of DNA that has the same nucleotide sequence as the mRNA (except the DNA has T where the RNA has U residues). Check out the supplemental resources for a diagram. Note that “sense strand” is sometimes used in different ways in the scientific literature, so it is critical to explicitly indicate what you mean when using this term.

Septum
The growth of the cell membrane and wall between opposite ends of a growing cell, ultimately separating the cell into two daughter cells.

Sexual PCR
PCR amplification in which similar, but not identical, DNA sequences are reassembled to obtain novel combinations of related, but variable sequences. When different combinations of a gene sequence are constructed, some of the resulting genes may possess improved characteristics. By repeating many rounds of PCR amplification and selection, an enormous amount of sequence variation can be obtained.

Shine-Delgarno sequence
A sequence in the mRNA which can pair with the ribosome facilitating the initiation of protein synthesis. (Named after the researchers who first described this sequence.)

Shotgun cloning
A cloning strategy that involves the insertion of random fragments of a large DNA molecule into a vector, resulting in a large number of different recombinant DNA molecules.

Shuttle vector
A vector that can replicate in the cells of more than one organism (e.g. in both E. coli and in yeast).

Sibs
An abbreviation for siblings.

Siblings
Two cells that arose by the division of a parent cell.

Sigma factor
A protein that functions as a subunit of bacterial RNA polymerases and is responsible for specificity of recognition of promoters. Different sigma factors allow recognition of different promoter sequences.

Signal transduction
Conditions that alter the conformation of a protein which regulates expression of other genes. Initially signal transduction was used to refer to extracellular conditions that alter the conformation of a membrane protein and cause it to relay the regulatory signal inside the cell, but more recently the term has been broadly applied to a variety of regulatory cascades.

Silent mutation
A mutation which changes the nucleotide sequence but does not cause a detectable change in the phenotype.

Similarity
Sequence identity between two nucleotide sequences. For example, 85% similarity means that 85 nucleotide positions out of 100 are identical in the two nucleotide sequences. Sequence similarity does not necessarily indicate that two sequences have common ancestry.

Single-strand DNA binding protein (ssb)
The small basic protein that has a high affinity for single-stranded DNA. Ssb protein protects single-stranded DNA from nuclease attack and inhibits it from reannealing into double-stranded DNA.

Site-directed mutagenesis
A method for introducing specific mutations at a defined site in a nucleotide sequence.

Site-specific recombination
Genetic exchange that occurs between particular, short DNA sequences. Site-specific recombination systems do not require RecA. Instead, each site-specific recombination system requires unique enzymes that catalyze the genetic exchange. Unlike RecA mediated recombination, site-specific recombination requires little sequence homology between the two DNA molecules. The best understood example is the integration of lambda into the E. coli chromosome by recombination between attP and attB catalyzed by the lambda integrase protein.

SNP
Defined regions of the genome where there are two or more nucleotide variations, each with 1% or greater prevalence in the population. SNPs can be used as genetic or physical markers.

SOS box
The operator sequence recognised by the LexA repressor protein.

SOS response
The coordinate induction of many genes in response to certain types of DNA damage. Many of the induced gene products facilitate repair of the damaged DNA, but the repair processes result in a high frequency of mistakes in the repaired DNA, a process often called error-prone repair. The SOS response in enteric bacteria is initiated by RecA protein, which becomes activated by DNA damage, and stimulates the autoproteolysis of several other proteins, including the LexA protein and the lambda cI repressor protein. The LexA protein is a global repressor that normally turns off expression of many other genes in the SOS regulon.

Southern blots
A method for detecting specific DNA fragments seperated on an agarose gel. DNA fragments are first seperated by electrophoresis through an agarose gel. After electrophoresis, the DNA in the gel is denatured by soaking the gel in an alkaline solution. Then a nitrocellulose or nylon membrane is layed on top of the agarose gel and absorbant paper is layered on top of the membrane. The aqueous solution passes from the agarose gel through the membrane into the absorbant paper by capillary action. The DNA moves with the aqueous solution but becomes trapped on the membrane. The DNA is then detected by annealing a labelled singlestranded DNA probe to the fragments of denatured DNA on the membrane, hybridization detected by autoradiography.

Specialized transduction
A method of gene transfer between bacteria in which a specific region of the bacterial donor DNA is carried by a phage. The host DNA carried by a specialized transducing phage arises by abbarent excision of a prophage. Thus, only regions of DNA adjacent to an integrated phage can be transferred by this method.

Spheroplast
Partial removal of the cell wall resulting in osmotically sensitive cells.

Spontaneous mutation
A mutation that occurs without known exposure to a mutagen.

Spore
A highly resistant, resting state of an organism. Under the proper condiditons s spore will germinate to form a viable, reproducing organism. Bacterial spores are often very resistant to heat and dessication.

Start (initiation) codon
The codon on mRNA where polypeptide synthesis is initiated. The most common start codon is AUG but sometimes GUG or rarely UUG can be used as a start codon.

Sticky (cohesive) ends
The two complementary single-stranded ends of a DNA duplex. For example, resulting from digestion with a Class II restriction endonuclease.

Stochastic
A random process; a process determined by a random distribution of probabilities.

Stop (nonsense) codon
A UAG, UAA. or UGA codons which is not representing any cognate aminoacyl tRNA in most organisms. When the ribosome encounters a stop codon in the mRNA, a termination factor interacts with the ribosome causing polypeptide synthesis to stop and the ribosome to dissociate from the mRNA.

Strain
An organism that is different from other organisms of the same species due to genetic differences. Strain is commonly used in two ways: (i) organisms of the same species that when initially isolated are found to have certain different properties (due to unknown mutations) are called different strains; (ii) derivatives of an organism that have distinct genotypes due to known mutations are called different strains.
Strand slippage
The denaturation and aberrant mispairing of a template strand during DNA replication. Results in frameshift mutations (see http://www.sci.sdsu.edu/~smaloy/MicrobialGenetics/topics/mutations/frame-shift.html).
Streptomycin
An antibiotic that inhibits protein synthesis in bacteria by binding to the S12 protein of the 30s ribosomal subunit and inhibiting translation. A high level of StrR can result from chromosomal mutations in the gene for the S12 protein (rpsL) which prevent streptomycin from binding to the ribosome. Only mutant ribosomes are StrR, so resistance to streptomycin is recessive to streptomycin sensitivity. Because streptomycin rapidly inhibits protein synthesis, when cells acquire the rpsL gene phenotypic expression is required before the cells become streptomycin resistant.

Stringency
Conditions affecting the hybridization of nucleotide sequences. Higher stringency conditions require more base pairing between the two sequences. Higher stringency conditions can be obtained by higher temperatures, highter salt concentrations, or addition of formamide.

Stringent response
The ability of a bacterium to limit the synthesis of tRNA and rRNA during amino acid starvation. The alarmones ppGpp and pppGpp are at least partially responsible for the stringent response. The concentrations of these alarmones are controlled by the relA and spoT gene products in E. coli.

Strong promoter
An efficient promoter that can direct synthesis of RNA transcripts at a relatively fast rate.

Structural gene
The portion of a gene encoding a functional polypeptide or RNA molecule.

DT>Structural protein
A protein which fulfill a purely structural role (i.e. not enzymatic). This includes phage capsid proteins, some ribosomal proteins, “histone-like” proteins, etc.

Stuffer fragment
The part of a lambda replacement vector that is removed during insertion of new DNA.

Substrate
A chemical recognized by an enzyme.

Substution mutation
A mutation that replaces one nucleotide in a DNA sequence with another nucleotide.

Subtraction library
A cDNA library that only contains those cDNAs that are expressed in a particular type of cell or tissue or under particular growth conditions. The cDNA common to all conditions is removed by hybridization with excess RNA from other cells (i.e. subtraction), leaving only the unique RNA behind.

Suicide plasmid
A plasmid that cannot replicate in a given host, used to force the; integration into host replicons of genetic determinants carried by the plasmid or phage. It is usually necessary to have a direct selection for the desired recombinants. See Allele exchange.

Supercoiled DNA
Double-stranded circular DNA in which either overwinding or underwinding of the duplex makes the circle twist. The conformation of a covalently closed-circular DNA molecule, which is coiled by torsional strain into the shape taken by a woundup elastic band.

Superinfection
The secondary infection by a phage in a cell already harbouring the same phage.

Superinfection exclusion
A process whereby the presence of one phage in a cell prevents the secondary infection by other. There are many different mechanisms of superinfection exclusion, including changes in cell surface receptors or the expression of a restriction system.

Suppression
The restoration (or partial restoration) of a wild-type phenotype by a second mutation. There are many different mechanisms of suppression (see the supplemental resources

Suppressor gene
A mutated gene which produces a product which reverses the effect of a previous specific mutation without actually correcting the original mutation in the DNA can be either intergenic or intragenic.

Suppressor mutation
A mutation that restores, partially or completely, the loss of function caused by another mutation. Many suppressor mutations are in genes encoding a transfer RNA species; the altered tRNA can recognise the original mutant codon and, during translation, insert an acceptable substitute amino acid into the polypeptide.

Suppressor tRNA
A mutant tRNA that recognizes a stop codon instead of the codon for the cognate amino acid. This property is sometimes, but not always, due to a base substitution in the anticodon.

Synapsis
The pairing of homologous chromosomes or of homologous chromosomal regions.

Synteny
Genes which occur in the same order on the chromosome of different species.

Sythetic lethal mutations
Two mutations are synthetically lethal if cells with either of the single mutations are viable but cells with both mutations are inviable. As with suppressor analysis, synthetic lethal mutations often indicate that the two mutations affect a single function or pathway.

Sythetic phenotype
A distinct phenotype that requires the presence of two mutations, and either of the mutations alone does not exhibit the same phenotype. Also note the defination of Synthetic lethal mutations.
Tandem duplication
A DNA sequence that is repeated in direct orientation.

3′-terminus
The end of a polynucleotide which carries the hydroxyl group attached to the 3′ position of the sugar.

5′-terminus
The end of a polynucleotide which carries the phosphate group attached to the 5′ position of the sugar.

T-DNA
The portion of the Ti plasmid transferred from Agrobacterium to the plant DNA.

Tandem duplication
Two adjacent copies of a DNA sequence.

Tandem repeats
Multiple adjacent copies of the same sequence.

Tautomeric shift
A reversible change in the position of a hydrogen atom in a molecule which results in the conversion of the molecule between different isomers. A shift between the keto group and a enoyl group in nucleotides can result in altered base-pairing.

Taxonomy
The classification of organisms.

Telomere
The terminal part of a linear chromosome. Replication of the ends of linear DNA molecules requires specialized enzymes or structures. Often the telomers have a DNA sequence with a single-stranded end that can fold into a hairpin structure.

Temperate phage
A phage that is capable of becoming a prophage in the bacterial host (i.e. maintain itself in a relatively quiescent state). Improperly but frequently called a lysogenic phage.

Temperature-sensitive mutation
A mutation that results in a gene product that is functional within a certain temperature range (e.g. at less than 30°C), but nonfunctional at different temperatures (e.g. at 42°C).

Template
A single-stranded polynucleotide (or region of a polynuceotide) that can be copied to produce a complementary polynucleotide.

Terminal redundancy
The presence of identical DNA sequences repeated at the two ends of DNA molecule (e.g. phage particles).

Terminator
A DNA sequence that results in termination of transcription. See Transcription terminator.

Terminus
The region of DNA sequences where DNA replication terminates.

Tetracycline (Tet)
An antibiotic that inhibits protein synthesis by preventing aminoacyl tRNA from binding to ribosomes. There are several possible mechanisms of Tetracycline resistance. TetR encoded by Tn10 and pBR plasmids is due to a membrane protein that actively transports tetracycline out of the cell.

Tetrad analysis
A method for establishing linkage relationships in fungi by analysing the four products from individual meiotic divisions.

Tetrad
The four products of a single meiosis.

Theta-replication
Replication of a circular molecule of double-stranded DNA by initiation at a unique origin and proceeding in one or both directions around the molecule. The resulting intermediate looks like the greek letter theta.

Three-factor cross
A method for determining the genetic map position of three linked loci based upon relative frequency of coinheritance of each locus during a cross between two strains with different allelic forms in each gene.

Thymine dimer
See pyrimidine dimer.

Ti plasmid
The large plasmid found in those Agrobacterium tumefaciens cells able to direct crown gall formation on certain species of plants.

Topoisomerase
An enzyme which introduces or removes overwinding or underwinding of the DNA circular duplex by causing a nick, rotating the strands, and then ligating them.

trans
Genes located on different DNA molecules present in the same cell (the opposite of cis). For example, one copy of a particular gene may reside on the chromosome and the second copy may reside on a plasmid.

Trans acting factor
A molecule that can diffuse through the cell to act at a distance from where it is made. Often used to distinguish gene products (protein or RNA) that regulate gene expression in trans vs the DNA site where the gene products binds.

Transcript
A strand of RNA copied from a DNA template.

Transcription bubble
A region where the double-stranded DNA is separated while RNA polymerase is actively transcribing RNA. A short region of RNA-DNA duplex is formed between the newly synthesized RNA and the template DNA in this region.

Trans-dimer synthesis
A process which permits nucleotides to be inserted opposite a pyrimidine dimer. Because this process is not based upon complementary base pairing, the wrong base pairs may be inserted, resulting in a mutation.

Transcription
The synthesis of RNA from a DNA template. Catalyzed by RNA polymerase.

Transcription terminator
A nucleotide sequence that acts as a signal for termination of transcription. There are two common types of transcription terminators: Rho-independant terminators (usually a stem-loop structure in the transcribed RNA followed by a run of U residues) are typically located at the end of operons, and Rho-dependant terminators (typically an unstructured region of RNA that, when untranslated, is recognized by Rho factor) are typically responsible for translational polarity.

Transcription unit
A region of DNA (a gene or an operon) transcribed as a single RNA.

Transcriptome
The complete set of RNA transcripts made by a cell under a particular condition. Typically determined by microarray analysis.

Transductant
A genetic recombinant formed by transduction.

Transduction
A method of gene transfer between bacteria in which the bacterial donor DNA is carried by a phage. There are two types of transduction: generalized transduction and specialized transduction. Generalized transduction can transfer of any region of the chromosome from the bacterial host into a recipient cell. Specialized transduction can only transfer regions of DNA adjacent to an integrated phage (prophage).

Transfection
The introduction of purified phage DNA into a bacterial cell by transformation or electroporation.

Transfer RNA (tRNA)
Adaptor molecules which translate the triplet code from the mRNA sequence into the corresponding chain of amino acids. tRNAs are short (about 74-95 bases), single-stranded RNA molecules that contain a high proportion of modified nucleosides. When drawn in two-dimensions, tRNAs can be folded into a characteristic cloverleaf structure with three stem-loop structures. The anticodon at the base of the second loop region. A specific amino acid is are added to the 3′ end of each tRNA by a specific aminoacyl tRNA synthetase. The aminoacylated tRNA binds to the ribosome-mRNA complex via interactions with the ribosome and, if the anticodon in the tRNA is properly paired with the complementary bases in the codon at that position, the amino acyl group is transferred to the growing polypeptide chain.

Transformation
Transfer of naked donor DNA into a cell.

Transformation frequency
The relative proportion of cells in a population that are transformed in a single experiment.

Transition mutation
A base substitution mutation where a purine is replaced by a different purine, or a pyrimidine is replaced by a different pyrimidine.

Translation
The assembly of amino acids into polypeptides using the genetic information encoded in the molecules of mRNA.

Translesion synthesis
A mechanism that resumes stalled replication due to a damage on the template strand. The stalled replicative polymerase is replaced by translesion polymerase(s) that synthesises a short stretch of DNA across the lesion. Once this occurs, the replicative polymerase resumes DNA synthesis.

Transposable element
A transposon or insertion sequence. An element that can insert in a variety of DNA sequences.

Transposase
An enzyme (or enzyme complex) required for the transposition of a particular transposable element. A transposase must recognize specific sites on the ends of a transposon, cut the transposon out of the original site, and insert the transposon into a new site.

Transposition
The movement of a discrete segment of DNA from one location in the genome to another.

Transposon
A genetic element which, in addition to encoding the proteins required for its own transposition, confers one or more new observable phenotypes (often resistance to one or more specific drugs) on the host cell.

Transposon tag
Use of a transposon insertion in a gene to follow the inheritance of the gene. Because transposons often express phenotypes that are simple to select and screen for (e.g. antibiotic resistance), it is often much easier to follow inheritance of the transposon insertion than the unmarked gene.

Transversion
A base substitution mutation where a pyrimidine replaces a purine, or a purine replaces a pyrimidine.

Triplet
A sequence of three nucleotides. Typically refers to the codons and the corresponding genetic code.

Truncation
To shorten. For example, a truncated protein results if a premature stop codon interrupts the gene.

Two-componant system
A regulatory mechanism that includes at least two functional activities defined as a sensor and a response regulator. Phosphorylation of the sensor domain is modulated in response to specific physiological stimulus. Phosophotransfer between a histidine residue on the sensor domain and an aspartate residue inÊthe response regulator domain determines the phosphorylation state of the response regulator. The phosphorylation state of the response regulator determines its physiological role (DNA binding, repression, activation, protein-protein interactions, or enzymatic activity). In many cases the two componants are present on separate proteins, but in some cases both componants are present in a single protein, and in other cases there are more than two proteins involved in the phosphotransfer reactions.

Two µm circle
A plasmid found in the yeast Saccharomyces cerevisiae and used as the basis for a series of cloning vectors.
uidA
The gene encoding Beta-glucuronidase (abbreviated GUS). Commonly used for constructing operon or gene fusions in organisms with high endogenous Beta-galactosidase activity. A variety of analogs exist that make it easy to detect GUS expression on solid medium and to assay the activity of the enzyme in cells.

Ultraviolet (UV) radiation
The part of the invivible electromagnetic spectrum (just below violet) with wavelengths between about 100-400 nm.

Undefined medium
A growth medium in which not all the components have been identified. Most “rich” media have a variety of complex, undefined componants.

Unequal cross-over
A recombination event that occurs between DNA molecules that are not fully aligned. For example, a crossover may occur between repeated DNA sequences resulting in the deletion or duplication the intervening DNA sequence.

Umber
The codon UGA. An less commonly used term for an opal codon.

Unidirectional replication
DNA replication that proceeds in only one direction along the DNA template.

Unselected marker
A genetic marker that may be co-inherited with an adjacent, selected marker but inheritance of the unselected marker is not demanded. For example, in a genetic cross you may select for one gene and screen for inheritance of an adjacent, unselected gene.

Up promoter mutation
A mutation that increasses expression from a promoter.

Upstream
A sequence located in front of a particular site relative to the direction of transcription and translation (i.e. located in the 5′ direction relative to a particular site). For example, the lac promoter is located upstream of the lacZ structural gene.

Upstream activator sequence (UAS)
A DNA sequence some distance in front of a gene that increases transcription of the gene. Such sequences often stimulate binding of RNA polymerase to the promoter.

Uracil-N-glycosylase
A repair enzyme that removes uracil from DNA by cleaving the bond between the base and the sugar backbone. This enzyme ensures that DNA contains T instead of U residues.

UV absorbance spectroscopy
A method for measuring the concentration of a compound by determining the amount of ultraviolet radiation absorbed by a sample.

UV reactivation
A phenomenon in which survival of an ultraviolet-irradiated phage is greater upon infecting a host that has also been irradiated with UV than upon infecting a host that has not been irradiated with UV. The increased survival in the UV irradiated host is due to the induction of the SOS-repair system in the host.

UvrABC
An enzyme complex that functions as an endonuclease, cutting the DNA on both sides of DNA lesions that distort the double-helix (for example, T-T dimers). The DNA fragment is subsequently excised allowing resynthesis and repairing the DNA damage.
Vector
A replicon that is useful for cloning DNA fragments so that they can be amplified or transferred to other cells. Common cloning vectors are derivatives of natural plasmids, phages, or viruses.

Viable
The ability of an organism to grow and divide.

Virion
An infectious virus particle.

Virulence
The relative ability of an organism to cause disease.

Virulence factor
Any gene product which enhances the ability of an organism to cause disease.

Virulence gene
Slang for a gene encoding a virulence factor.

Virulent phage
A bacteriophage which always grows lytically.

Virus
A small, infectious, obligate intracellular parasite. The virus genome is composed of either DNA or RNA. Within an appropriate host cell, the viral genome is replicated and uses cellular systems to direct the synthesis of other viral components. Progeny viruses are formed by de novo assembly from the newly synthesized components within the host cell. Transmission of the progeny viruses occurs by release from the host cell, and infection of new host cells.

Vitamin
An organic compound that is required in relatively small amounts for growth of an organism. Vitamins often function as coenzymes.

VSP repair
“Very short patch” DNA repair. A DNA repair mechanism that corrects G-T mismatches arising from deamination of 5-methyl cytosine in enteric bacteria. A short DNA fragment including the mismatch is excised and resynthesized.
Watson-Crick rules
The normal base pairing rules for DNA and RNA: A pairs with T or U, and G pairs with C.

Weigle reactivation
The increased survival of phage after UV irradiation if they infect cells that have previously been exposed to a lose dose of UV. Due to induction of UV repair systems in the infected cells.

Western blot
Transfer of proteins from an acrylamide gel onto a membrane filter for the detection with specific antibodies.

Wild-type
A strain used as a standard reference to compare any mutant derivatives. A wild-type strain may have certain nutritional requirements depending upon the species. Often a wild-type strain is simply one of the most convient strains of a particular species obtained from nature.

Wobble
A hypothesis proposed by Francis Crick to explain how one tRNA may recognize two different codons that differ in the third position. The three bases in the anticodon of each tRNA are antiparallel to the three bases of the codon in the mRNA. Normal Watson-Crick base pairing occurs between the first two bases of the codon with the complementary bases of the anticodon. However, the first (5′) base of the anticodon can pair with the third (3′) base of the codon in different ways: in this position of the anticodon G can pair with either C or U in the mRNA, U can pair with either A or G in the mRNA, and I can pair with A, C, or U in the mRNA.
X-gal
A common abbreviation for 5-bromo-4-chloro-3-indolyl-ß-D-galactoside. A sensitive, color indicator for ß-galactosidase. X-gal is a colorless compound but upon hydrolysis by beta-galactosidase releases an indolyl moiety. This product is not colored, but dimerizes after oxidation to form an insoluble and highly colored indigo dye. The oxidation is promoted by atmospheric oxygen, hence the color does not form anaerobically. (X-gal is also sometimes written as Xgal, without the hyphen.)

X-glu
A common abbreviation for 5-bromo-4-chloro-3-indolyl-glucuronide. A color indicator for beta-Glucuronidase (GUS). X-glu (AKA X-gluc) is a colorless compound but upon hydrolysis by GUS the indolyl moiety is oxidized to form a blue colored product. GUS is often used as a reporter gene in organisms that have high background levels of beta-galactosidase, often due to multiple genes encoding lacZ homologues. (See X-gal)

X-over
An abbreviation for cross-over.

X-P
A common abbreviation for 5-bromo-4-chloro-3-indolyl phosphate. A sensitive, color indicator for alkaline phosphatase activity. X-P is a colorless compound but upon hydrolysis by a phosphatase the indolyl moiety is released, and upon oxidization it forms a blue colored product. (See X-gal)
Yeast
A unicellular form of fungi. Some fungi (for example Saccharomyces cerevisiae) are only known to reproduce as yeast while other fungi (for example, Candida albicans) are dimorphic, reproducing as yeast under certain conditions and as filamentous mycelia under other growth conditions. Because it is so widely used in studies of Eukaryotic genetics, the term yeast often refers to S. cerevisiae when a specific genus is not indicated.

Yeast artificial chromosome (YAC)
A cloning vector which contains sequences from a yeast chromosome required for DNA replication and segregration. Often used for cloning very large fragments of DNA.

Yeast episomal plasmid (YEp)
A yeast vector carrying the 2 µm circle origin of replication.

Yeast extract
A water soluble preparation extracted from common yeast. Yeast extract is rich in amino acids, peptides, B vitamins, and trace elements. Commonly used in rich media.

Yeast integrative plasmid (YIp)
A yeast vector that relies on integration into the host chromosome for replication.

Yeast replicative plasmid (YRp)
A yeast vector that carries a chromosomal origin of replication.

Yeast two-hybrid system
An approach developed by Stan Fields and colleagues in 1989 to identify protein-protein interactions in vivo. Proteins (aka “prey”) that interact with other, known proteins (aka “bait”) are identified by using a reporter system that relies upon interaction between the two proteins. A variety of versions of this system are available, but the basic format involves the construction of two distinct hybrid proteins fused to different reporter genes: in the first the “bait” protein is fused to a transcription factor, and in the second the “prey” protein is fused to a related transcription factor. If the bait and prey proteins interact the two reporter genes fused to the proteins are brought into proximity with each other, producing a specific signal.

Be the first to comment - What do you think?  Posted by admin - April 27, 2010 at 12:24 am

Categories: Genetic, Glossary   Tags: , , , ,

Powered by WordPress Lab