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28 Cards in this Set

  • Front
  • Back
anticipation
increasing severity or earlier age of onset of a genetic trait in succeeding generations. For example, symptoms of a genetic disease may become more severe as the trait is passed from generation to generation
codominance
type of allelic interaction in which the heterozygote simultaneously expresses traits of both homozygotes
complementation
two different mutations in the heterzygous condition are exhibited as the wild-type phenotype; indicates that the mutations are at different loci
complementation test
test designed to determine wheter two different mutations are at the same locus (are allelic) or at different loci (are nonallelic). Two individuals that are homozygous for two independently derived mutations are crossed, producing F1 progeny that are heterozygous for the mutations. If the mutations are at the same locus, the F1 will have a mutant phenotype. If the mutations are at different loci, the F1 will have a wild-type phenotype.
continuous characteristic
displays a large number of possible phenotypes that are not easily distinguished , such as human height
cytoplasmic inheritance
inheritance of characteristics encoded by genes located in the cytoplasm. Because the cytoplasm is usually contributed entirely by only one parent, most cytoplasmically inherited characteristics are inherited from a single parent.
discontinuous characteristic
exhibits only a few easily distinguished phenotypes. An example is seed shape in which seeds are either round or wrinkled
epigenetics
phenonmena due to alterations to DNA that do not include changes in the base sequence; often affect the way in which the DNA sequences are expressed. Such alterations are often stable and heritable in the sense that they are passed from one cell to another
epistasis
type of gene interaction in which a gene at one locus masks or suppresses the effects of a gene at different locus
epistatic gene
masks or suppresses the effect of a gene at a different locus
expressivity
degree to which a trait is expressed
gene interaction
interactions between genes at different loci that affect the same characteristic
genetic maternal effect
determines the phenotype of an offspring. With genetic maternal effect, an offspring inherits genes for the characteristics from both parents, but the offspring's phenotype is determined not by its own genotype but by the nuclear genotype of its mother
genomic imprinting
differential expression of a gene that depends on the sex of the parent that transmitted the gene. If the gene is inherited from the father, its expression is defferent from that if it is inherited from the mother
hypostatic gene
gene that is masked or suppressed by the action of a gene at a different locus
incomplete penetrance
refers to a genotype that does not always express the expected phenotype. Some individuals possess the genotype for a trait but do not express the phenotype
lethal allele
causes the death of an individual organism, often early in development, and so the organism does no appear in the progeny of a genetic cross. Recessive lethal alleles kill individual organisms that are homozygous for the allele; domminant lethals kill both heterozygotes and homozygotes.
multifactrial characteristic
determined by multiple genes and environmental factors
multiple alleles
presence in a group of individuals of more that two alleles at a locus. Although, for the group, the locus has more than two alleles, each member of the group has only two of the possible alleles.
norm of reaction
range of phenotypes produced by a particular genotype in different environmental conditions
penetrance
percentage of individuals with a particular genotype that expresses the phenotype expected of that genotype
phenocopy
phenotype that is produced by environmental effects and is the same as the phenotype produced by a genotype
pleiotropy
a single genotype influences multiple phenotypes
polygenic characteristic
encoded by genes at many loci
quantitative characteristic
continuous characteristic; desplays a large number of possible phenotypes, which must be described by a quantitative measurement
sex-influenced characteristic
encoded by autosomal genes that are more readily expressed in one sex. For example, an autosomal dominant gene may have higher penetrance in males than in females or an autosomal gene may be dominant in males but recessive in females
sex-limited characteristic
encoded by autosomal genes and expressed in only one sex. Both males and females carry genes for sex-limited characteristics, but the characteristics appear in only one of the sexes
temperature-sensitive allele
expressed only at certain temperatures