| S (Svedberg unit) |
| A unit of sedimentation velocity, commonly
used to describe molecular units of various sizes (because sedimentation
velocity is related to size). |
| S-9 mix |
| A liver-derived cell extract used in the
Ames test to activate or inactivate chemicals in a test for mutagens
and potential carcinogens. |
| sampling distribution
|
| The distribution of frequencies with which
various possible events could occur or a probability distribution
defined by a particular mathematical expression . |
| sarcoma |
| tumour of mesodermal origin (eg muscle,
bone, cartilage). |
| SAR |
| scaffold attachment region - the position
along eukaryotic DNA where it is anchored to the central scaffold
of the chromosome. |
| satellite |
| A terminal section of a chromosome, separated
from the main body of the chromosome by a narrow constriction. |
| satellite chromosome
|
| chromosome that seems to be an addition
to the normal genome. |
| satellite DNA |
| DNA that forms a separate band in a bouyant
density gradient because of its different nucleotide composition
(A:T rich DNAs are less dense than G:C rich DNAs). Highly repetitive
eukaryotic DNA primarily located around centromeres. Satellite DNA
usually has a different buoyant density than the rest of the cell's
DNA. |
| saturation mutagenesis
|
| Induction and recovery of large numbers
of mutations in one area of a genome, or in one biological function,
in the hope of identifying all the genes in that area, or affecting
that function. |
| scaffold |
| The eukaryotic chromosome structure remaining
when DNA and histones have been removed; made from nonhistone proteins.
The central framework of a chromosome to which the DNA solenoid
is attached as loops; composed largely of topoisomerase. |
| scanning hypothesis |
| Proposed mechanism by which the eukaryotic
ribosome recognizes the initiation region of an mRNA after binding
the 5' capped end of it. The ribosome scans the mRNA for the initiation
codon. |
| scientific method |
| A procedure used by scientists to test hypotheses
by making predictions about the outcome of an experiment before
the experiment is performed. The results provide support or refutation
of the hypothesis. |
| screening technique |
| A technique to determine the genotype or
phenotype of an organism. |
| second division segregation
(SDS) |
| The allele arrangement (2+2+2+2) in the
spores of Ascomycetes with ordered spores that indicates a crossover
between a locus and its centromere. A pattern of ascospore genotypes
for a gene pair showing that the two alleles segregate into different
nuclei only at the second meiotic division, as a result of a single
crossover between that gene pair and its centromere; can only be
detected in a ordered ascus. See First division segregation |
| second-site mutation
|
| The second mutation of a double mutation
within a gene. In many cases, the second-site mutation suppresses
the first mutation, so that the double mutant has the wild-type
phenotype. |
| secondary oocyte |
| A cell formed by meiosis I in female animals.
|
| secondary sexual character
|
| The sex-associated phenotype of somatic
tissues in sexually dimorphic animals. |
| secondary spermatocyte
|
| The product of the first meiotic division
in male animals. |
| secondary structure |
| The alpha-helical or beta-sheet configuration
of the polypeptide backbone of a protein. |
| sector |
| An area of tissue or colony whose phenotype
is detectably different from the surrounding tissue or colony phenotype.
|
| sedimentation |
| The sinking of a molecule under the opposing
forces of gravitation and buoyancy. |
| segmentation |
| The process by which the correct number
of segments are established in a developing segmented animal. |
| segregation |
| (1) Cytologically, the separation of homologous
chromosomes into different cells at cell division. |
| (2) Genetically, the production of two separate
phenotypes, corresponding to two alleles of a gene, either in different
individuals (meiotic segregation) or in different tissues (mitotic
segregation). |
| segregation, rule of
|
| Mendel's first principle describing how
genes are passed from one generation to the next. |
| segregational load |
| Genetic load caused when a population is
segregating less fit homozygotes because of heterozygote advantage.
|
| segregational petite
|
| A petite that in a cross with wild-type
produces 50% petite and 50% wild-type progeny; caused by a nuclear
mutation. |
| selection |
| (1) Genetic methods for obtaining desired
strains often employ selective procedures based on differential
survival under particular nutritional or envirnomental conditions.
See conditional mutation. |
| (2) Genetic breeding methods start by selecting
particular desirable phenotypes as parents for the next generation.
|
| (3) See also natural selection. |
| selection coefficient
(s) |
| The proportional excess or deficiency of
fitness of one genotype in relation to another genotype. |
| selection differential
|
| The difference between the mean of a population
and the mean of the individuals selected to be parents of the next
generation. |
| selection progress |
| The difference between the mean of a population
and the mean of the offspring in the next generation born to selected
parents. |
| selection-mutation equilibrium
|
| An equilibrium allele frequency resulting
from the balance between selection against the allele and mutation
recreating this allele. |
| selective medium |
| A culture medium that is enriched with a
particular substance to allow the growth of particular strains of
organisms. |
| selective neutrality
|
| A situation in which different alleles of
a certain gene confer equal fitness. |
| selective system |
| An experimental technique that enhances
the recovery of specific (usually rare) genotypes. |
| self |
| The fusion of male and female gametes from
the same individual. See self-fertilization. |
| self-assembly |
| The ability of certain multimeric biological
structures to assemble from their component parts through random
movements of the molecules and formation of weak chemical bonds
between surfaces with complementary shapes. |
| self-fertilization |
| Fertilization in which the two gametes are
from the same individual. |
| selfish DNA |
| A segment of the genome with no apparent
function other than to ensure its own replication. |
| semiconservative replication
|
| The mode by which DNA replicates. Each strand
acts as a template for a new double helix. The established model
of DNA replication in which each double-stranded molecule is composed
of one parental strand and one newly polymerized strand. See template.
|
| semisterility (half sterility)
|
| The phenotype of individuals heterozygotic
for certain types of chromosome aberration; expressed as a reduced
number of viable gametes and hence reduced fertility. Nonviability
of a proportion of gametes or zygotes. |
| Sequence tagged site
(STS) |
| Any site in a chromosome or genome that
is identified by a known unique DNA sequence. STSs can be used to
form genetic maps by standard mapping procedures. |
| Ser |
| Serine (an amino acid). |
| sex chromosome |
| A chromosome whose presence or absence is
correlated with the sex of the bearer; a chromosome that plays a
role in sex determination. Heteromorphic (different shaped, eg X
and Y) chromosomes whose distribution in a zygote determines the
sex of the organism. |
| sex determination |
| The genetic or environmental process by
which the sex of an individual is established. |
| sex linkage |
| The location of a gene on a sex chromosome.
|
| sex linked |
| The inheritance pattern of loci located
on the sex chromosomes (usually the X chromosome in XY species);
also refers to the loci themselves. |
| sex reversal |
| A syndrome known in humans and mice in which
chromosomally XX individuals develop as males. In some cases, sex
reversal is now known to be due to the translocation of the testis-determining
region of the Y chromosome to the tip of the X chromosome in such
individuals. |
| sex switch |
| A gene, normally found on the Y chromosome
in mammals, that directs the indeterminate gonads toward development
as testes. See testis-determining factor. |
| sex-controlled trait
|
| Traits that appear more of time in one sex
than in the other. |
| sex-determining region
Y (SRY) |
| The sex switch or testis-determining factor
in human beings located on the Y chromosome. (Sry in mice.) |
| sex-lethal |
| A gene in Drosophila, located on the X chromosome,
that is a sex switch directing development toward femaleness when
it is in the on state. It is regulated by numerator and denominator
elements that act to influence the genic balance equation (X/A).
|
| sex-limited trait |
| Trait expressed in only one sex. It may
be controlled by sex linked or autosomal loci. |
| sex-ratio phenotype |
| A trait in Drosophila whereby females produce
mostly if not only daughters. |
| sexduction |
| Sexual transmission of donor Escherichia
coli chromosomal genes on the fertility factor. A process whereby
a bacterium gains access to and incorporates foreign DNA brought
in by a modified F factor during conjugation. |
| sexual selection |
| The forces determined by mate choice acting
to cause one genotype to mate more frequently than another genotype.
|
| Shine-Delgarno hypothesis
|
| A proposal that prokaryotic mRNA is aligned
at the ribosome by complementarity between the mRNA upstream from
the initiation codon and the 3' end of the 16S rRNA. |
| shotgun technique |
| Cloning a large population of different
DNA fragments, known to contain a fragment of interest, as a prelude
to selecting or screening for that one particular clone containing
the fragment of interest for intensive study. |
| shuttle vector |
| A vector (e.g. a plasmid) constructed in
such a way that it can replicate in at least two different host
species (eg a prokaryote and a eukaryote). A DNA recombined into
such a vector can be tested or manipulated in several cell types.
|
| siblings(sibs) |
| Brothers and sisters. |
| sickle-cell anemia |
| Potentially lethal human disease, inherited
as an autosomal recessive, caused by a mutation in a gene coding
for the beta subunit of the oxygen-transporting protein haemoglobin.
Under conditions of low oxygen tension, the altered beta-globin
molecule causes haemoglobin to aggregate forming rod-like arrays
that distort the cell membrane forcing red blood cells to become
sickle-shaped. The sickled red blood cells are damaged and rapidly
removed from the circulation causing anaemia. |
| sigma factor |
| The protein that gives promoter-recognition
specificity to the RNA polymerase core enzyme of bacteria. |
| signal hypothesis |
| The major mechanism whereby proteins that
insert into or cross a membrane are synthesized by a membrane-bound
ribosome. The first thirteen to thirty-six amino acids synthesized,
termed a signal peptide, are recognized by a signal recognition
particle that draws the ribosome to the membrane surface by interaction
with a docking protein. The signal peptide may later be removed
from the protein. |
| signal sequence |
| The N-terminal sequence of a secreted protein,
which is required for transport through the cell membrane. |
| signal transduction cascade
|
| Refers to a series of sequential events,
such as protein phosphorylations, consequent upon binding of ligand
by a transmembrane receptor, that transfer a signal through a series
of intermediate molecules until final regulatory molecules, such
as transcription factors, are modified in response to the signal.
|
| silent mutation |
| mutation in which the function of the protein
product of the gene is unaltered. |
| SINE |
| Short interspersed element. A type of small
dispersed repetitive DNA sequence (eg Alu family in the human genome)
found throughout a eukaryotic genome. |
| single-strand binding
protein |
| Protein that binds to single-stranded DNA
usually near the replication fork to stabilize the single strands.
|
| sister-chromatid exchange
(SCE) |
| An event similar to crossing over that can
occur between sister chromatids at mitosis or at meiosis. |
| site-specific recombination
|
| A crossover event, such as the integration
of phage lambda, that requires homology of only a very short region
and uses an enzyme specific for that recombination. Recombination
occurring between two specific sequences that need not be homologous;
mediated by a specific recombination system. |
| skew |
| A distortion of the shape of the normal
distribution toward one side or the other. |
| snRNP |
| Small nuclear ribonucleoprotein (RNA plus
protein) particle. Component of the spliceosome, the intron-removing
apparatus in eukaryotic nuclei . |
| sociobiology |
| The study of the evolution of social behavior
in animals. |
| solenoid structure |
| The supercoiled arrangement of DNA in eukaryotic
nuclear chromosomes produced by coiling the continuous string of
nucleosomes (about 7 nucleosomes per turn). |
| somatic cell |
| A cell that is not destined to become a
gamete; a cell whose genes will cannot be passed on to future generations.
|
| somatic doubling |
| A disruption of the mitotic process that
produces a cell with twice the normal chromosome number. |
| somatic hypermutation
|
| The occurrence of a high level of mutation
in the variable regions of immunoglobulin genes. |
| somatic mutation |
| A mutation occurring in a somatic cell.
|
| somatic-cell genetics
|
| Asexual genetics, involving study of somatic
mutation, mitotic crossing-overand segregation. |
| somatic-mutation theory
|
| A theory to account for the high degree
of antibody variability. It suggests that mutation of a basic immunoglobulin
gene accounts for all the different types of immunoglobulins produced
by B lymphocytes. See germ-line theory. |
| somatostatin |
| A human growth hormone. |
| SOS box |
| The region in the promoter of various genes
that is recognized by the LexA repressor. Release of repression
results in the induction of the SOS response. |
| SOS repair |
| The error-prone process whereby gross structural
DNA damage is circumvented by allowing replication to proceed past
the damage through imprecise polymerization. |
| SOS response |
| Repair systems (recA; uvr) induced by the
presence of single-stranded DNA that usually occurs from postreplicative
gaps caused by various types of DNA damage. The RecA protein, stimulated
by single-stranded DNA, is involved in the inactivation of the LexA
repressor thereby inducing the response. |
| Southern blot |
| Transfer of electrophoretically separated
fragments of DNA, after denaturation, from the gel to an absorbent
sheet of material, such as nitrocellulose, to which the DNA binds.
The sheet is immersed in a solution containing a labeled probe that
will hybridize to fragment(s) of interest. The method was first
devised by E. M. Southern to transfer DNA fragments from an agarose
gel to a nitrocellulose paper for hybridization, but similar transfer
methods are now also used for transfering RNA or protein to papers
of a variety of types followed by hybridization (RNA) or labeled
antibody treatment (protein) to identify specific molecules. |
| spacer DNA |
| Regions of non-transcribed DNA between transcribed
repeated genes such as ribosomal RNA genes in eukaryotes. Its function
is probably to do with ensuring the high rates of transcription
associated with these genes. |
| specialized (restricted)
transduction |
| The situation in which a particular phage
will transduce only specific regions of the bacterial chromosome.
Form of transduction based on faulty looping out by a temperate
phage. Only loci neighbouring the attachment site can be transduced.
See generalized transduction. |
| speciation |
| A process whereby over time one species
evolves into a different species (anagenesis) or whereby one species
diverges to become two or more species (cladogenesis). |
| species |
| A group of organisms belong to the same
biological species if they are capable of interbreeding to produce
fertile offspring. However the biological test of a species is not
always available, and so there is also a morphological species concept
based on anatomical similarities. |
| specific-locus test |
| A system for detecting recessive mutations
in diploids. Normal individuals treated with mutagen are mated to
testers that are homozygous for the recessive alleles at a number
of specific loci; the progeny are then screened for recessive phenotypes.
|
| sperm cell |
| The male gamete. |
| spermatid |
| The four products of meiosis in males that
develop into sperm. |
| spermatocyte |
| (1) (Zoological) A cell which undergoes
meiosis and thereby produces spermatids. See primary spermatocyte
and secondary spermatocyte. |
| (2) (Botanical) A cell that becomes converted
to a spermatozoid (a small motile male gamete with flagella) without
intervention of cell division. |
| spermatogenesis |
| The process of sperm production. |
| spermatogonium |
| A cell type in the testes of male vertebrates
that gives rise to primary spermatocytes by mitosis. |
| spermiogenesis |
| The process by which spermatids mature into
sperm cells. |
| spindle |
| The set of tubulin fibers that appear to
move eukaryotic chromosomes during division. The microtubule apparatus
that controls chromosome movement during mitosis and meiosis. |
| spiral cleavage |
| The cleavage process in molluscs and some
invertebrates whereby orientation of the spindle at mitosis is at
an angle to the original egg axis. |
| spirillum |
| A spiral bacterium. |
| spliceosome |
| Protein-RNA complex that removes introns
from eukaryotic nuclear RNAs. |
| splicing |
| The reaction that removes introns and joins
together exons in eukaryotic nuclear primary RNA transcripts. |
| spontaneous mutation
|
| A mutation occurring in the absence of mutagens,
usually due to errors in the normal functioning of cellular enzymes.
|
| spore |
| (1) In plants and fungi, sexual spores are
the haploid cells produced by meiosis. |
| (2) In fungi, asexual spores are somatic
cells that are cast off to act either as gametes or as the initial
cells for new haploid individuals. |
| sporophyte |
| The diploid sexual-spore-producing generation
in the life cycle of plants. The stage in which meiosis occurs.
The stage of a plant life cycle that produces spores by meiosis
and alternates with the gametophyte stage. |
| stabilizing selection
|
| A type of selection that removes individuals
from both ends of a phenotypic distribution thus maintaining the
same distribution mean. |
| stacking |
| The packing of the flattish nitrogen base-pairs
at the centre of the DNA double helix. |
| staggered cuts |
| The cleavage of two opposite strands of
duplex DNA at points near one another. |
| standard deviation |
| The square root of the variance. |
| standard error of the
mean |
| The standard deviation divided by the square
root of the sample size. It is the standard deviation of a sample
of means. |
| stasipatric speciation
|
| Instantaneous speciation caused by polyploidy.
|
| statistic |
| A computed quantity characteristic of a
population, such as the mean. |
| statistical distribution
|
| The array of frequencies of different quantitative
or qualitative classes in a population. |
| statistics |
| Measurements of attributes of a sample from
a population. See parameters. |
| stem-loop structure |
| A lollipop-shaped structure formed when
a single-stranded nucleic acid molecule loops back on itself to
form a complementary double helix (stem) topped by a loop. |
| steroid receptor |
| A family of related proteins that act as
transcription factors when bound to their cognate hormone ligands.
Not all members of this family actually bind to steroids; the name
derives from the first family member that was discovered, which
was a steroid hormone receptor. |
| stochastic |
| A process with an indeterminate or random
element as opposed to a deterministic process that has no random
element. |
| strain |
| A pure-breeding lineage, usually of haploid
organisms, bacteria, or viruses. |
| stringent factor |
| A protein catalyzing the formation of an
unusual nucleotide (guanosine tetraphosphate, ppGpp) during the
stringent response under amino acid starvation conditions. |
| stringent response |
| A translational control mechanism of prokaryotes
that represses tRNA and rRNA synthesis during amino acid starvation.
|
| structural gene |
| A gene encoding the amino acid sequence
of a protein. Non-regulatory gene. |
| submetacentric chromosome
|
| A chromosome whose centromere lies between
its middle and its end but closer to the middle. |
| subtelocentric chromosome
|
| A chromosome whose centromere lies between
its middle and its end but closer to the end. |
| subvital gene |
| A gene that causes the death of some proportion
(but not all) of the individuals that express it. |
| sum rule |
| The probability that one or the other of
two mutually exclusive events will occur is the sum of their individual
probabilities. The rule that states that the probability of the
occurrence of mutually exclusive events is the sum of the probabilities
of the individual events. |
| supercoil |
| A closed double-stranded DNA molecule that
is twisted on itself. |
| supercoiling |
| Negative (tending to unwind the helix) or
positive (tending to wind the helix) coiling of double-stranded
DNA that differs from the relaxed state. |
| supergene |
| Several loci, which usually control related
aspects of the phenotype, in close physical association. |
| superinfection |
| Phage infection of a cell that already harbours
a prophage. |
| supersuppressor |
| A mutation that can suppress a variety of
other mutations; typically a nonsense suppressor. |
| suppressive petite |
| A petite that in a cross with wild-type
produces progeny of which variable non-Mendelian proportions are
petite. |
| suppressor gene |
| A gene that, when mutated, apparently restores
the wild-type phenotype to a mutation at another locus. |
| suppressor mutation |
| A mutation that counteracts the effects
of another mutation. A suppressor maps at a different site than
the mutation it counteracts, either within the same gene or at a
more distant locus. Different suppressors act in different ways.
|
| survival of the fittest
|
| In evolutionary theory the survival of only
those organisms best able (fittest) to obtain and utilize resources.
This phenomenon is the cornerstone of Darwin's theory of evolution
by natural selection. |
| Svedberg unit |
| A unit of sedimentation rate during centrifugation.
Abbreviation is S as in 50S. |
| swivelase |
| speciation in which the evolution of reproductive
isolating mechanisms occurs within the range and habitat of the
parent species. This form of speciation may be common in parasites.
|
| synapsis |
| The point-by-point pairing of homologous
chromosomes during zygotene or in certain Dipteran tissues (eg Drosophila
salivary glands) that undergo endomitosis. Close pairing of homologs
at meiosis. |
| synaptonemal complex
|
| A proteinaceous complex that apparently
mediates synapsis during zygotene stage and then disintegrates.
A complex structure that unites homologous chromosomes during the
prophase of meiosis. |
| syncytial blastoderm
|
| In insects, the syncytial stage of blastoderm
preceding the formation of cell membranes around the individual
nuclei of the early embryo. |
| syncytium |
| A single cell with many nuclei. |
| synteny |
| All loci on one chromosome are said to be
syntenic (literally on the same ribbon). Loci may appear to be unlinked
by conventional genetic tests for linkage but still be syntenic.
|
| synteny test |
| A test that determines whether two loci
belong to the same linkage group (ie are syntenic) by observing
concordance (occurence of markers together) in hybrid cell lines.
|
| synthetic medium |
| A chemically defined substrate upon which
organisms are grown. |