27.7: Key Terms
- Page ID
- 146321
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- gene variations that arise by mutation and exist at the same relative locations on homologous chromosomes
- autosomes
- any of the non-sex chromosomes
- blending theory of inheritance
- hypothetical inheritance pattern in which parental traits are blended together in the offspring to produce an intermediate physical appearance
- codominance
- in a heterozygote, complete and simultaneous expression of both alleles for the same characteristic
- continuous variation
- inheritance pattern in which a character shows a range of trait values with small gradations rather than large gaps between them
- dihybrid
- result of a cross between two true-breeding parents that express different traits for two characteristics
- discontinuous variation
- inheritance pattern in which traits are distinct and are transmitted independently of one another
- dominant
- trait which confers the same physical appearance whether an individual has two copies of the trait or one copy of the dominant trait and one copy of the recessive trait
- F1
- first filial generation in a cross; the offspring of the parental generation
- F2
- second filial generation produced when F1 individuals are self-crossed or fertilized with each other
- genotype
- underlying genetic makeup, consisting of both physically visible and non-expressed alleles, of an organism
- heterozygous
- having two different alleles for a given gene on the homologous chromosome
- homozygous
- having two identical alleles for a given gene on the homologous chromosome
- hybridization
- process of mating two individuals that differ with the goal of achieving a certain characteristic in their offspring
- law of dominance
- in a heterozygote, one trait will conceal the presence of another trait for the same characteristic
- law of independent assortment
- genes do not influence each other with regard to sorting of alleles into gametes; every possible combination of alleles is equally likely to occur
- law of segregation
- paired unit factors (i.e., genes) segregate equally into gametes such that offspring have an equal likelihood of inheriting any combination of factors
- model system
- species or biological system used to study a specific biological phenomenon to be applied to other different species
- monohybrid
- result of a cross between two true-breeding parents that express different traits for only one characteristic
- P0
- parental generation in a cross
- phenotype
- observable traits expressed by an organism
- product rule
- probability of two independent events occurring simultaneously can be calculated by multiplying the individual probabilities of each event occurring alone
- Punnett square
- visual representation of a cross between two individuals in which the gametes of each individual are denoted along the top and side of a grid, respectively, and the possible zygotic genotypes are recombined at each box in the grid
- recessive
- trait that appears “latent” or non-expressed when the individual also carries a dominant trait for that same characteristic; when present as two identical copies, the recessive trait is expressed
- reciprocal cross
- paired cross in which the respective traits of the male and female in one cross become the respective traits of the female and male in the other cross
- sum rule
- probability of the occurrence of at least one of two mutually exclusive events is the sum of their individual probabilities
- test cross
- cross between a dominant expressing individual with an unknown genotype and a homozygous recessive individual; the offspring phenotypes indicate whether the unknown parent is heterozygous or homozygous for the dominant trait
- trait
- variation in the physical appearance of a heritable characteristic