a.b.c.d.e.f.g.h.i.j.k.l.m.n.o.p.q.r.s.t.u.v.w.x.y.z
P (peptidyl) site
The site on the ribosome occupied by the peptidyl-tRNA just before peptide bond formation.
P element
A Drosophila transposable element that has been used as a tool for insertion mutagenesis and for germline transformation.
P1
Parental generation.
pachynema (pachytene stage)
The stage of prophase 1 of meiosis in which chromatids are first distinctly visible.
palindrome
A sequence of letters, words, phrases, or nucleotides that reads the same regardless of direction, for instance what Adam said to Eve "Madam I'm Adam". The DNA sequence of type II restriction endonuclease recognition sites (eg EcoRI 5'GAATTC3') and the binding sites of many other DNA binding proteins (eg. catabolite activator protein (CAP) binding site 5'GTGAGTTAGCTCAC3') are not true palindromes but in double stranded form are similar and have two-fold rotational symetry.
panmictic
Referring to unstructured (random-mating) populations.
paracentric inversion
An inversion not involving the centromere. A chromosomal inversion that does not include the centromere.
paralogous genes
Two genes or clusters of genes at different chromosomal locations in the same organism that have structural similarities indicating that they derived from a common ancestral gene.
paramecin
A toxin liberated by a killer Paramecium.
parameters
Measurements of attributes of a population.
parapatric speciation
speciation in which the evolution of reproductive isolating mechanisms occurs when a population enters a new niche or habitat within the range of the parent species.
parental ditype (PD)
A tetrad type containing two different genotypes, both of which are parental. A spore arrangement in Ascomycetes that contains only the two non-recombinant-type ascospores.
parthenogenesis
The production of offspring by a female with no genetic contribution from a male. The development of an individual from an unfertilized egg that did not arise by meiotic chromosome reduction .
partial digest
A restriction digest that has not been allowed to go to completion and thus contains pieces of DNA with some restriction endonuclease sites that have not yet been cleaved.
particulate inheritance
The model proposing that genetic information is transmitted from one generation to the next in discrete units (particles) so that the character of the offspring is not a smooth blend of essences from the parents (See blending inheritance).
Pascal's triangle
A triangular array of numbers made up of the coefficients of the binomial expansion.
path diagram
A modified pedigree showing only the direct line of descent from common ancestors.
pathogen
An organism that causes disease in another organism.
patroclinous inheritance
Inheritance in which all offspring have the nucleus-based phenotype of the father.
pattern formation
The developmental processes by which the complex shape and structure of higher organisms occurs.
pedigree
A family tree drawn with standard genetic symbols, showing inheritance patterns for specific phenotypic characters. A representation of the ancestry of an individual or family; a family tree.
penetrance
The proportion of individuals with a specific genotype who manifest that genotype at the phenotype level.
peptide bond
A bond joining two amino acids.
peptidyl transferase
The enzymatic centre in the ribosome responsible for peptide bond formation during translation.
pericentric inversion
An inversion that involves the centromere. A chromosomal inversion that includes the centromere.
permissive condition
Environmental condition under which a conditional mutation shows the wild-type phenotype.
permissive temperature
A temperature at which temperature-sensitive mutants are normal.
PEST hypothesis
The short life-time of a protein is signaled by a region rich in the amino acids proline (P); glutamic acid (E); serine (S); or threonine (T).
petite
A yeast mutation producing small colonies and altered mitochondrial functions. In cytoplasmic (neutral and suppressive) petites the mutation is a deletion in mitochondrial DNA, while in segregational petites the mutation occurs in nuclear DNA.
petite mutation
A mutation of yeast that produces small (petite) anaerobic-like colonies.
Phe
Phenylalanine (an amino acid).
phenocopy
A phenotype that is not genetically controlled but looks like a genetically controlled phenotype. An environmentally induced phenotype that resembles the phenotype produced by a mutation.
phenotype
(1) The form taken by some character (or group of characters) in a specific individual.
(2) The detectable outward manifestations of a specific genotype.
(3) The observable attributes of an organism.
phenotypic sex determination
Sex determination by non-genetic means.
phenotypic variance
Variance of phenotype due to genotypic and environmental factors combined.
phenylketonuria(pku)
A human metabolic disease caused by a mutation in a gene coding for a phenylalanine processing enzyme (phenylalanine hydroxylase), which leads to accumulation of phenylalanine and mental retardation if not treated; inherited as an autosomal recessive phenotype.
pheromone
A chemical signal, analogous to a hormone, that passes information between individuals.
Philadelphia chromosome
A translocation between the long arms of chromosomes 9 and 22, often found in the white blood cells of patients with chronic myeloid leukemia.
phosphodiester bond
A bond between a two sugar groups and a phosphate group; such bonds form the sugar-phosphate-sugar backbone of DNA and RNA. A diester bond (between phosphoric acid and two sugar molecules) linking two nucleotides together to form the nucleotide polymers DNA and RNA.
photoreactivation
The process whereby dimerized pyrimidines (usually thymines) in DNA are restored by an enzyme (deoxyribodipyrimidine photolyase) that requires light energy.
phyletic gradualism
The process of gradual evolutionary change over time.
phylogenetic tree
A diagram showing evolutionary lineages of organisms.
piebald
A mammalian phenotype in which patches of skin are unpigmented because of lack of melanocytes; generally inherited as an autosomal dominant.
pilus (plural pili)
A conjugation tube; a hollow hair-like appendage of a donor Escherichia coli cell that acts as a bridge for transmission of donor DNA to the recipient cell during conjugation.
plant breeding
The application of genetic analysis to development of plant lines better suited for human purposes.
plaque
A clear area on a bacterial lawn, left by lysis of the bacteria through progressive infections by a phage and its descendants. Clear area on a bacterial lawn caused by cell lysis due to viral attack.
plasmid
Autonomously replicating extrachromosomal DNA molecule. An autonomous self-replicating genetic particle usually of circular double-stranded DNA.
plastid
A chloroplast prior to the development of chlorophyll.
plate
(1) A flat dish used to culture microbes.
(2) To spread cells over the surface of solid medium in a plate.
pleiotropic mutation
A mutation that has effects on several different characters.
pleiotropy
The phenomenon whereby a single mutation affects several apparently unrelated aspects of the phenotype.
point mutation
A mutation that can be mapped to one specific site within a locus. A small mutation that consists of the replacement (transition or transversion); addition; or deletion (frameshift) of one or a few bases.
Poisson distribution
A mathematical expression giving the probability of observing various numbers of a particular event in a sample when the mean probability of that event on any one trial is very small.
poky mutation
A mutation of Neurospora that produces a petite-like phenotype.
polar body
A small cell (which eventually disintegrates) that is the by-product of meiosis in female animals. One functional ovum and potentially three polar bodies result from meiosis of each primary oocyte.
polar gene conversion
A gradient of conversion frequency along the length of a gene.
polar granules
Cytoplasmic granules localized at the posterior end of a Drosophila oocyte and early embryo. These granules are associated with determinants of the germ-line and posterior structures.
polar mutation
A mutation that affects the transcription or translation of part of the gene or operon downstream of the mutant site. For example, nonsense mutations, frameshift mutations, and insertion sequence(IS)-induced mutations.
polarity
Meaning directionality and referring either to an effect seen in only one direction from a point of origin or to the fact that linear entities (such as a single strand of DNA or RNA or a protein) have ends (5' and 3'; N and C) that differ from each other.
polarity gene
A mitochondrial gene with alleles that are preferentially found in daughter mitochondria after a recombinational event between mitochondria.
Pollen grain
The male gametophyte in higher plants.
poly(A) tail
A string of adenine nucleotides added to the 3' end of eukaryotic mRNA after transcription.
poly-dA/poly-dT technique
A method of inserting DNA into a vector by adding poly-dA to the linearised vector and poly-dT to the DNA of interest. Also feasible with poly-dG and poly-dC.
polyacrylamide
A material used to make gels for separation of mixtures of macromolecules by electrophoresis.
polycistronic
Referring to prokaryotic messenger RNAs that contain several cistrons within the same mRNA transcript.
polycistronic mRNA
An mRNA that codes for more than one protein.
polydactyly
More than five fingers and/or toes. Inherited as an autosomal dominant phenotype.
polymerase chain reaction (PCR)
A powerful method for amplifying specific DNA segments which exploits certain features of DNA replication. For instance replication requires a primer and specificity is determined by the sequence and size of the primer. The method amplifies specific DNA segments by cycles of template denaturation; primer addition; primer annealing and replication using thermostable DNA polymerase. The degree of amplification achieved is set at a theoretical maximum of 2^N, where N is the number of cycles, eg 20 cycles gives a theoretical 1048576 fold amplification.
polymerize
To form a complex compound (polymer) by linking together many smaller elements (residues).
polymorphism
The occurrence in a population (or among populations) of several phenotypic forms associated with alleles of one gene or homologs of one chromosome. See genetic polymorphism.
polynucleotide phosphorylase
An enzyme that can polymerize nucleotide diphosphates without the need for a primer. The function of this enzyme in vivo is probably in its reverse role as an RNA exonuclease.
polypeptide
A chain of linked amino acids; a protein.
polyploid
A cell or an organism having three or more chromosome sets.
polysaccharide
A biological polymer composed of sugar subunits for example, starch or cellulose.
polysome
The configuration of several ribosomes simultaneously translating the same mRNA. Shortened form of the term polyribosome.
polytene chromosome
A giant chromosome produced by an endomitotic process in which, following synapsis of the two homologues, multiple rounds of replication produce chromatids that remain synapsed together in a haploid number of chromosomes. Large chromosome consisting of many chromatids formed by rounds of endomitosis following synapsis of the two homologues.
population
A group of organisms of the same species relatively isolated from other groups of the same species. See deme.
position effect
Used to describe a situation in which the phenotype expressed by a gene is altered by changes in the position of the gene within the genome. For instance genes translocated to regions of heterochromatin are often not expressed.
position-effect variegation
Variegation caused by the inactivation of a gene in some cells through its abnormal juxtaposition with heterochromatin.
positive assortative mating
A situation in which like phenotypes mate more commonly than expected by chance.
positive control
Regulation mediated by a protein that is required for the activation of a transcription unit.
positive interference
When the occurrence of one crossover reduces the probability that a second will occur in the same region .
postreplicative repair
A DNA repair process initiated when DNA polymerase bypasses a damaged area. enzymes in the rec system are used.
post-transcriptional modification
Changes in eukaryotic mRNA, tRNA or other RNAs made after transcription has been completed. The changes to mRNA include addition of a 5'cap and 3' polyA tail and removal of introns, and to tRNA include modification of bases and removal of introns.
preemptor stem
A configuration of leader transcript mRNA that allows transcription in attenuator-controlled amino acid operons.
pre-mRNA
The first (primary) transcript from a protein coding gene is often called a pre-mRNA and contains both introns and exons. Pre-mRNA requires splicing (removal) of introns to produce the final mRNA molecule containing only exons.
Pribnow box
Relatively invariant sequence of six nucleotides (concensus TATAAT) in prokaryotic promoters centred at the position minus 10 (10 base pairs upstream from the transcription start site).
primary oocyte
A cell that undergoes meiosis in female animals.
primary spermatocyte
A cell that undergoes the first meiotic division in male animals. See secondary spermatocyte.
primary structure
The sequence of polymerized amino acids in a protein.
primary transcript
The product of eukaryotic transcription before post-transcriptional modifications take place.
primase
An enzyme that creates an RNA primer for initiation of DNA replication.
primer
A short sequence (of RNA or DNA) from which DNA replication can initiate. May be either a synthetic DNA or RNA or a length of RNA synthesized in vivo by primase.
primosome
A complex of two proteins, a primase and a helicase, that initiates RNA primers on the lagging DNA strand during DNA replication.
prion
Protein infectious agent associated with several neurological diseases (scrapie; kuru; Creutzfeld-Jakob syndrome; Alzheimer's disease). Each disease has a different prion.
Pro
Proline (an amino acid).
probability
The expectation of the occurrence of a particular event.
probability theory
The conceptual framework concerned with quantification of probabilities. See probability.
probe
Defined nucleic acid (DNA or RNA) that can be used to identify, usually through autoradiography, specific DNA or RNA molecules bearing the complementary sequence. A labeled (radioactive; antigen; enzyme; fluorescent) nucleic acid complementary to the sequence being searched for in a restriction digest, genome library, northern blot or in situ hybridization.
processivity
The ability of an enzyme to repetitively continue its catalytic function without dissociating from its substrate.
product of meiosis
One of the (usually four) cells formed by the two meiotic divisions.
product rule
The probability of two independent events occurring simultaneously is the product of the individual probabilities. The rule stating that the probability of the occurrence of independent events is the product of their separate probabilities.
proflavin
A mutagen that tends to produce frameshift mutations.
progeny testing
Breeding of offspring to determine their genotypes and that of their parents.
prokaryote
An organism lacking a true nucleus, such as a bacterium or a blue-green alga.
prokaryotic cell
A cell having no nuclear membrane and hence no separate nucleus.
promoter
A regulatory region a short distance upstream from the 5' end of a transcription start site that acts as the binding site for RNA polymerase. A region of DNA to which RNA polymerase binds in order to initiate transcription.
proofread
Literally to read for the purpose of detecting errors for later correction. DNA polymerase has 3' to 5' exonuclease activity which is used during polymerization to remove nucleotides it has recently added if they are incorrectly paired, and is a correcting ability to remove errors in replication.
prophage
A phage chromosome inserted as part of the linear structure of the DNA chromosome of a bacterium. A temperate phage integrated into the host chromosome.
prophase
The early stage of nuclear division during which chromosomes condense and become visible. The initial stage of mitosis or meiosis in which chromosomes become visible and the spindle apparatus forms.
proplastid
Mutant plastids that do not grow and develop into chloroplasts.
propositus
The person through whom a pedigree was discovered.
proto-oncogene
The non-activated form of a cellular oncogene in an untransformed cell. A gene that, when mutated or otherwise affected, becomes an oncogene.
protoplast
A plant cell whose wall has been removed.
prototroph
A strain of organisms that will proliferate on minimal medium (compare auxotroph).
provirus
A virus chromosome integrated into the DNA of the host cell.
pseudoallele
allele that is functionally but not structurally allelic, that is wild-type recombinants can be recovered by intragenic recombination from heterozygotes containing two different pseudoalleles.
pseudoautosomal gene
A gene that occurs on both sex-determining heteromorphic chromosomes.
pseudodominance
The sudden appearance of a recessive phenotype in a pedigree, due to deletion of a masking dominant gene. The phenomenon in which a recessive allele shows itself in the phenotype when only one copy of the allele is present, as in hemizygous alleles or in deletion heterozygotes .
pseudogene
An inactive gene derived from an ancestral active gene.
pulse-chase experiment
An experiment in which cells are grown in radioactive medium for a brief period (the pulse) and then transferred to nonradioactive medium for a longer period (the chase).
pulsed-field gel electrophoresis
An electrophoretic technique in which the gel is subjected to electrical fields alternating between different angles, allowing very large DNA fragments to snake through the gel, and hence permitting efficient separation of mixtures of such large fragments.
punctuated equilibrium
The evolutionary process involving long periods without change (stasis) punctuated by short periods of rapid speciation.
Punnett square
A diagrammatic representation of a particular cross used to predict the progeny of the cross. A grid used as a graphic representation of the progeny zygotes resulting from different gamete fusions in a specific cross.
pure-breeding line or strain
A group of identical individuals that always produce offspring of the same phenotype when intercrossed.
purines
A type of nitrogen base; the purine bases in DNA and RNA are adenine and guanine.
pyrimidine
Nitrogenous bases of which thymine is found in DNA; uridine in RNA; and cytosine in both.