Genetics R - Z
Terms
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- R plasmid
- a plasmid containing one or several transposons that bear resistance genes
- random genetic drift
- changes in allele frequency that result because the genes appearing in offspring do not represent a perfectly representative sampling of the parental genes
- random mating
- mating between individuals where the choice of a partner is not influenced by the genotypes (with respect to specific genes under study)
- reading frame
- the codon sequence that is determined by reading nucleotides in groups of three from some specific start codon
- realized heritability
- the ratio of the single-generation progress of selection to the selection differential of the parents
- reannealing
- spontaneous realignment of two single DNA strands to re-form a DNA double helix that had been denatured
- receptor element
- a controlling element that can insert into a gene (making it a mutant) and can also exist (thus making the mutation unstable); both functions under the influence of the regulator element
- recessive allele
- an allele whose phenotype effect is not expressed in a heterozygote
- recessive phenotype
- the phenotype of a homozygote for the recessive allele; the parental phenotype that is not expressed in a heterozygote
- reciprocal translocation
- a translocation in which part of one chromosome is exchanged with a part of a separate nonhomologous chromosome
- recombinant
- an individual or cell with a genotype produced by recombination
- recombinant DNA
- a novel DNA sequence formed by the combination of two nonhomologous DNA molecules
- RF
- recombinant frequency
- recombinant frequency (RF)
- the proportion (or percentage) of recombinant cells or individuals
- recombination (in general)
- any process in a diploid or partially diploid cell that generates new gene or chromosomal combinations not found in that cell or in its progenitors
- recombination (at meiosis)
- the process that generates a haploid product of meiosis whose genotype is different from either of the two haploid genotypes that constituted the meiotic diploid
- recombinational repair
- the repair of a DNA lesion through a process, similar to recombination, that uses recombination enzymes
- recon
- a region of a gene within which there can be crossing-over; now known to be a nucleotide pair
- reduction division
- a nuclear division that produces daughter nuclei each having one-half as many centromeres as the parental nucleus
- regression
- it arises from dominance, gene interaction, and nongenetic influences on traits
- regression coefficient
- the slope of the straight line that most closely relates two correlated variables
- regulatory genes
- genes that are involved in turning on or off the transcription of structural genes
- another name for repetitive DNA
- redundant DNA
- redundant (repetitive) DNA
- DNA sequences that are present in many copies per chromosome set
- replication fork
- the point at which the two strands of DNA are separated to allow replication of each strand
- replicon
- a chromosomal region under the influence of one adjacent replication-initiation locus
- reporter gene
- a gene whose phenotypic expression is easy to monitor
- repressor protein
- a molecule that binds to the operator and prevents transcription of an operon
- repulsion conformation
- two linked heterozygous gene pairs in the arrangement A b/ a B
- resolving power
- the ability of an experimental technique to distinguish between two genetic conditions
- restriction enzyme
- an endonuclease that will recognize specific target nucleotide sequences in DNA and break the DNA chain at those points
- restrictive conditions
- environmental conditions under which a conditional mutant shows the mutant phenotype
- retrovirus
- an RNA virus that replicates by first being converted into double-stranded DNA
- reverse transcriptase
- an enzyme that catalyzes the synthesis of a DNA strand from an RNA template
- reversion
- the production of a wild-type gene from a mutant gene
- RFLP mapping
- a technique in which DNA restriction fragment length polymorphisms are used as reference loci for mapping in relation to known genes or other RFLP loci
- RNA
- ribonucleic acid
- rRNA
- ribosomal RNA
- ribosome
- composed of proteins plus rRNA
- ribonucleic acid (RNA)
- a single-stranded nucleic acid similar to DNA but having ribose sugar rather than deoxyribose sugar and uracil rather than thymine as one of the bases
- RNA polymerase
- an enzyme that catalyzes the synthesis of an RNA strand from a DNA template
- ribosomal RNA (rRNA)
- a class of RNA molecules, coded in the nucleolar organizer, that have an integral (but poorly understood) role in ribosome structure and function
- S
- Svedberg unit
- Svedberg unit (S)
- a unit of sedimentation velocity, commonly used to describe molecular units of various sizes
- satellite
- a terminal section of a chromosome separated from the main body of the chromosome by a narrow constriction
- satellite chromosomes
- chromosomes that seem to be additions to the normal genome
- satellite DNA
- DNA that forms a separate band in a density gradient because of its different nucleotide composition
- scaffold
- the central core of a eukaryotic nuclear chromosome, from which DNA loops extend
- SCE
- sister-chromatid exchange
- sister-chromatid exchange (SCE)
- an event similar to crossing-over that can occur between sister chromatids at mitosis or at meiosis; detected in harlequin chromosomes
- secondary structure of a protein
- a spiral or zigzag arrangement of the polypeptide chain
- second-division segregation pattern
- a pattern of ascospore genotypes for a gene pair showing that the two alleles separate into different nuclei only at the second meiotic division as a result of a crossover between that gene pair and its centromere
- second-site mutation
- the second mutation of a double mutation within a gene
- sector
- an area of tissue whose phenotype is detectably different from the surrounding tissue phenotype
- sedimentation
- the sinking of a molecule under the opposing forces of gravitation and buoyancy
- cytological segregation
- the separation of homologous structures
- genetic segregation
- the production of two separate phenotypes corresponding to two alleles of a gene either in meiotic or mitotic segregation
- segregational petite
- a petite that in a cross with wild-type produces ½ wild-type progeny; caused by a nuclear mutation
- selection coefficient (s)
- the proportional excess or deficiency of a population and the mean of the individuals selected to be parents of the next generation
- 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
- 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
- to fertilize eggs with sperms from the same individual
- 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
- semiconservative replication
- the established model of DNA replication in which each double-stranded molecule is composed of one parental strand and one newly polymerized strand
- semisterility
- the phenotype of individuals heterozygotic for certain types of chromosome aberration; expressed as a reduced number of viable gametes and hence reduced fertility
- senDNA
- an amplified section of mtDNA found in senescent Podospora cultures; circular and plasmid-like in nature
- 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
- sex linkage
- the location of a gene on a sex chromosome
- sexduction
- sexual transmission of a donor E. coli chromosomal genes on the fertility factor
- shotgun technique
- cloning a large number of different DNA fragments as a prelude to selecting one particular clone type for intensive study
- shuttle vector
- a vector constructed in such a way that it can replicate in at least two different host species, allowing a DNA segment to be tested or manipulated in several cellular settings
- signal sequence
- the N-terminal sequence of a secreted protein, which is required for transport through the cell membrane
- silent mutation
- mutation in which the function of the protein product of the gene is unaltered
- site-specific recombination
- recombination occurring between two specific sequences that need not be homologous, and mediated by a specific recombination system
- S-9 mix
- a liver-derived supernatant used in the Ames test to activate or inactivate mutagens
- solenoid structure
- the supercoiled arrangement of DNA in eukaryotic nuclear chromosomes
- somatic cell
- a cell that is not destined to become a gamete; a "body cell," whose genes will not be passed on to future generations
- somatic mutation
- a mutation occurring in a somatic cell
- somatic-cell genetics
- asexual genetics, involving study of somatic mutation, assortment, and crossing-over, and of cell fusion
- somatostatin
- a human growth hormone
- SOS repair
- the error-prone process whereby gross structural DNA damage is circumvented by allowing replication to proceed past the damage through imprecise polymerization
- spacer DNA
- repetitive DNA found between genes; its function is unknown
- specialized (restricted) transduction
- the situation in which a particular phage will transduce only specific regions of the bacterial chromosome
- specific-locus test
- a system for detecting recessive mutations in diploids; normal individuals treated with mutagen are mated to testers that ar homozygous for the recessive alleles at a number of specific loci; the progeny are then screened for recessive phenotypes
- spindle
- the set of microtubular fibers that appear to move eukaryotic chromosomes during division
- splicing
- the reaction that removes introns and joins together exons in RNA
- spontaneous mutation
- a mutation occurring in the absence of mutagens, usually due to errors in the normal functioning of cellular enzymes
- spore
- in fungi, 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, i.e. the stage in which meiosis occurs
- stacking
- the packing of the flattish nitrogen bases at the center 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
- 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
- strain
- a pure-breeding lineage, usually of haploid organisms, bacteria, or viruses
- structural gene
- a gene encoding the amino-acid sequence of a protein
- 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
- supercoil
- a closed double-stranded DNA molecule that is twisted on itself
- superinfection
- phage infection of a cell that already harbors 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 mutation
- a mutation that counteracts the effects of another mutation; maps at a different site than the mutation it counteracts, either within the gene or at a more distant locus
- synapsis
- close pairing of homologs at meiosis
- synaptonemal complex
- a complex structure that unites homologs during the prophase of meiosis
- syncytium
- a single cell with many nuclei
- T
- thymine, or thymidine
- tandem duplication
- adjacent identical chromosome segments
- tautomeric shift
- the spontaneous isomerization of a nitrogen base to an alternative hydrogen-bonding condition, possibly resulting in a mutation
- T-DNA
- a portion of the Ti plasmid that is inserted into the genome of the host plant cell
- telocentric chromosome
- a chromosome having the centromere at one end
- telophase
- the late stage of nuclear division when daughter nuclei re-form
- temperate phage
- a phage that can become a prophage
- temperature-sensitive mutation
- a conditional mutation that produces the mutant phenotype in one temperature range and the wild-type phenotype in another temperature range
- template
- a molecular "mold" that shapes the structure or sequence of another molecule
- teratogen
- an agent that interferes with normal development
- teratoma
- a tumor composed of a chaotic array of different tissue types
- terminal redundancy
- in phage, a linear DNA molecule with single-stranded ends that are longer than is necessary to close the DNA circle
- tertiary structure of a protein
- the folding or coiling of the secondary structure to form a globular molecule
- testcross
- a cross of an individual of unknown genotype or a heterozygote (or a multiple heterozygote) to a tester individual
- tester
- an individual homozygous for one or more recessive alleles; used in a testcross
- testicular feminization
- the creation of an apparent female phenotype in an XY individual as a result of an X-linked mutation
- tetrad
- the four haploid product cells from a single meiosis
- tetrad analysis
- the use of tetrads to study the behavior of chromosomes and genes during meiosis
- tetraparental mouse
- a mouse that develops from an embryo created by the experimental fusion of two separate blastulas
- tetraploid
- a cell having four chromosome sets; an organism composed of such cells
- tetratype (T)
- a tetrad type containing four different genotypes, two parental two and two recombinant
- Thr
- threonine (an amino acid)
- three-point testcross
- a testcross involving one parent with three heterozygous gene pairs
- thymidine
- the nucleoside having thymine as its base
- thymine dimer
- a pair of chemically bonded adjacent thymine bases in DNA; the cellular processes that repair this lesion often make errors that create mutations
- Ti plasmid
- a circular plasmid of Agrobacterium tumifaciens that enables the bacterium to infect plant cells and produce a tumor (crown gall tumor)
- totipotency
- the ability of a cell to proceed through all the stages of development and thus produce a normal adult
- trans conformation
- in a heterozygote involving two mutant sites within a gene or gene cluster
- transcription
- the synthesis of RNA using a DNA template
- transdetermination
- a specific change in the fate of an imaginal disk that can occur when the disk is cultured
- transduction
- the movement of genes from a bacterial donor to a bacterial recipient using a phage as the vector
- transformation (first definition)
- the directed modification of a genome by the external application of DNA from a cell of different genotype
- transformation (second definition)
- conversion of normal higher eukaryotic cells in tissue culture to a cancer-like state of uncontrolled division
- transgenic organism
- one whose genome has been modified by externally-applied new DNA
- transient diploid
- the stage of the life cycle of predominantly haploid fungi (and algae) during which meiosis occurs
- transition
- for example, GC -> AT
- translation
- the ribosome-mediated production of a polypeptide chain whose amino-acid sequence is derived from the codon sequence of an mRNA molecule
- translocation
- the relocation of a chromosomal segment in a different position in the genome
- transmission genetics
- the study of the mechanisms involved in the passage of a gene from one generation to the next
- transposable genetic element
- a general term for any genetic unit that can insert into a chromosome, exit, and relocate; includes insertion sequences, transposons, some phages, and controlling elements
- transposon
- a mobile piece of DNA that is flanked by terminal repeat sequences and typically bears genes coding for transposition functions
- transversion
- for example, GC -> TA
- triplet
- the three nucleotide pairs that compose a codon
- triploid
- a cell having three chromosome sets, or an organism composed of such cells
- trisomic
- basically, a diploid with an extra chromosome of one type, producing a chromosome number of the form 2n + 1
- tritium
- a radioactive isotope of hydrogen
- tRNA
- transfer RNA
- transfer RNA (tRNA)
- a class of small RNA molecules that bear specific amino acids to the ribosome during translation
- Trp
- tryptophan (an amino acid)
- truncation selection
- a breeding technique in which individuals in whom quantitative expression of a phenotype is above or below a certain value are selected as parents for the next generation
- Turner's syndrome
- an abnormal human female phenotype produced by the presence of only one X chromosome (XO)
- twin spot
- a pair of mutant sectors within wild-type tissue, produced by a mitotic crossover in an individual of appropriate heterozygous genotypye
- 2 µ ( 2 micron) plasmid
- a naturally-occurring extragenomic circular DNA molecule; engineered to form the basis for several types of gene vectors in yeast
- found in some yeast cells with a circumferance of 2µ
- 2µ (2 micron) plasmid
- Tyr
- tyrosine (an amino acid)
- unequal crossover
- a crossover between homologs that are not perfectly aligned
- uniparental inheritance
- the transmission of certain phenotypes from one parental type to all the progeny; such inheritance is generally produced by organelle genes
- unstable mutation
- a mutation that has a high frequency of reversion; a mutation caused by the insertion of a controlling element, whose subsequent exit produces a reversion
- uracil
- a pyrimidine base that appears in RNA in place of thymine found in DNA
- URF (unassigned reading frame)
- a DNA region, identified by nucleotide sequencing studies, that has an initiation and a termination codon, and therefore presumably represents a gene, but for which no phenotype or function is known
- uridine
- the nucleoside having uracil as its base
- Val
- valine (an amino acid)
- variable
- a property that may have different values in various cases
- variance
- a measure of the variation around the central class of a distribution; the average squared deviation of the observations from their mean value
- variable region
- the part of the antibody that binds to the antigen
- variant
- an individual organism that is recognizably different from an arbitrary standard type in that species
- variate
- a specific numerical value of a variable
- variation
- the differences among parents and their offspring or among individuals in a population
- variegation
- the occurrence within a tissue of sectors with differing phenotypes
- vector
- in cloning, the plasmid or phage chromosome used to carry the cloned DNA segment
- viability
- the probability that a fertilized egg will survive and develop into an adult organism
- virulent phage
- a phage that cannot become a prophage; infection by such a phage always leads to lysis of the host cell
- wild-type
- the genotype or phenotype that is found in nature or in the standard laboratory stock for a given organism
- wobble
- the ability of certain bases at the third position of an anticodon in tRNA to form hydrogen bonds in various ways, causing alignment with several possible codons
- X linkage
- the presence of a gene on the X chromosome but not on the Y
- X-and-Y linkage
- the presence of a gene on both the X and Y chromosomes (rare)
- X-ray crystallography
- a technique for deducing molecular structure by aiming a beam of X rays at a crystal of the test compound and measuring the scatter of rays
- Y linkage
- the presence of a gene on the Y chromosome but not on the X (rare)
- zygote
- the unique diploid cell that will divide mitotically to create a differentiated diploid organism
- zygotic induction
- the sudden release of a lysogenic phage from an Hfr chromosome when the prophage enters the F¯ cell, and the subsequent lysis of the recipient cell