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
N segment
Sequence of nucleotides added in a template-independant fashion at the joining junctions of heavy-chain immunoglobulin genes.
N-end rule
The life span of a protein is determined by its amino-terminal (N-terminal) amino acid.
natural selection
The process in nature whereby one genotype leaves more offspring than another genotype because of superior life history attributes (fitness)such as survival or fecundity.
nearest-neighbour analysis
A technique of transferring radioactive atoms between adjacent nucleotides in DNA used to demonstrate that the two strands of DNA run in opposite directions.
negative assortative mating
Preferential mating between phenotypically different partners.
negative control
Transcription regulation mediated by factors that block, turn down or turn off transcription.
negative interference
The phenomenon whereby a crossover in a particular region enhances the occurrence of other apparent crossovers in the same region of the chromosome.
neo-darwinism
The merger of classical Darwinian evolution with population genetics.
neomorph
Mutant showing a novel substance or structure not found in wild-types.
neoplasm
New growth of abnormal tissue.
neurofibromatosis
A human disease with tumours of nerve cells all over the body and pigmented spots in the skin. The allele generally arises from germinal mutation, but it is inherited as an autosomal dominant.
Neurospora
A pink mold, commonly found growing on old food.
neutral gene hypothesis
The hypothesis that most genetic variation in natural populations is not maintained by selection because most alleles have equal fitness.
neutral mutation
(1) A mutation that has no effect on the Darwinian fitness of its carriers.
(2) A mutation that has no phenotypic effect.
neutral petite
A petite yeast that produces all wild-type progeny when crossed with wild-type.
nicking
Nuclease action to sever the sugar-phosphate backbone in one DNA strand but not the other at one specific site.
nitrocellulose filter
A type of filter used to bind DNA for hybridization.
nitrogen base
Type of molecule that forms an important part of nucleic acid, composed of a nitrogen-containing ring structure. Hydrogen bonds between bases in opposing complementary strands link the two strands of a DNA double helix.
non-Mendelian ratio
An unusual ratio of progeny phenotypes that does not reflect the simple operation of Mendel's laws; for example, mutant:wild-type ratios of 3:5, 5:3, 6:2, or 2:6 in tetrads indicate that gene conversion has occurred.
non-disjunction
The failure of a pair of homologous chromosomes to separate properly during meiosis. The failure of homologues (at meiosis) or sister chromatids (at mitosis) to separate properly to opposite poles, that is two chromosomes or chromatids go to one pole and none to the other.
non-histone protein
The protein remaining in chromatin after the histones are removed. The scaffold structure is made of nonhistone proteins.
non-linear tetrad
A tetrad in which the meiotic products are in no particular order.
non-parental ditype (NPD)
A spore arrangement in Ascomycetes that contains only the two recombinant-type ascospores (assuming two segregating loci). A tetrad type containing two different genotypes, both of which are recombinant.
non-recombinant
In mapping studies the offspring that have alleles arranged as in the original parents are non-recombinants.
nonsense codon
One of the mRNA sequences (UAA, UAG, UGA) that signals the termination of translation. A codon for which no normal tRNA molecule exists. The presence of a nonsense codon causes termination of translation (ending polypeptide chain synthesis). There are three nonsense codons are called amber(UAG) ochre(UAA) and opal(UGA).
nonsense mutation
A mutation that alters a gene so as to produce a .
nonsense suppressor
A mutation in the anticodon of tRNA that alters the anticodon so it is now complementary to a nonsense codon allowing the tRNA to insert its cognate amino acid at this nonsense codon during translation.
norm of reaction
The pattern of phenotypes produced by a given genotype under different environmental conditions.
normal distribution
Any of a family of bell-shaped frequency curves whose relative position and shape are defined on the basis of the mean and standard deviation.
Northern blot
Transfer of electrophoretically separated RNA molecules from a gel onto an absorbent sheet, which is then immersed in a labeled probe that will hybridize to an RNA of interest to reveal its presence. See Southern blotting.
nuclear transplantation
The technique of placing a nucleus from another source into an enucleated cell.
nuclease
One of the several classes of enzymes that degrade nucleic acid. An enzyme that can degrade DNA or RNA by breaking phosphodiester bonds. See endonucleases; exonucleases.
nuclease hypersensitive site
Region of eukaryotic chromosome DNA that is specifically vulnerable to nuclease attack perhaps because it is not wrapped in histone as nucleosomes.
nucleoid
A DNA mass within a chloroplast or mitochondrion.
nucleolar organizer
The chromosomal region around which the nucleolus forms, a site of tandem repeats of the rRNA gene. A region (or regions) of the chromosome set physically associated with the nucleolus and containing rRNA genes.
nucleolus
The globular nuclear organelle formed at the nucleolar organizer. Site of ribosome construction. An organelle found in the nucleus, containing rRNA and multiple copies of the genes coding for rRNA.
nucleoprotein
The substance of eukaryotic chromosomes consisting of proteins and nucleic acids.
nucleoside
A sugar-base compound that is a nucleotide precursor. Nucleotides are nucleoside phosphates. A nitrogen base linked to a sugar molecule.
nucleosome
A nu body; the basic unit of eukaryotic chromosome structure; a ball of eight histone molecules wrapped about by two coils of about 220 base pairs of DNA. Arrangement of DNA and histones forming regular spherical structures in eukaryotic chromatin.
nucleotide
Subunit that polymerizes into nucleic acids (DNA or RNA). Each nucleotide consists of a nitrogenous base; a sugar; and one to three phosphate groups.
nucleotide pair
A pair of complementary nucleotides (one in each strand of DNA) that are joined by hydrogen bonds.
nucleotide-pair substitution
The replacement of a specific nucleotide pair by a different pair; often mutagenic.
nucleus
The membrane bound organelle containing the genome of eukaryotes organized into chromosomes.
null allele
An allele whose effect is either an absence of normal gene product at the molecular level or an absence of normal function at the phenotypic level.
null hypothesis
The statistical hypothesis that states that there are no differences between observed and expected data.
nullisomic
A diploid cell or individual missing both copies of the same chromosome. A cell or individual with one chromosomal type missing, with a chromosome number such as n-1 or 2n-2.
numerator element
Genes on the X chromosome in Drosophila that regulate the sex switch (sxl) to the on condition (femaleness). Refers to the numerator of the X/A (number of X chromosomes/autosomes) genic balance equation.
nurse cell
A sister cell of an oocyte in insects. Nurse cells produce the bulk of the cytoplasmic contents of the mature oocyte.