Genetics Unit Test Vocabulary Flashcards
genetics
the science of heredity and of the mechanisms by which traits are passed from parents to offspring
heredity
the passing of genetic traits from parent to offspring
trait
a genetically determined characteristic
pollination
the transfer of pollen from the male reproductive structures (the anthers) to the tip of a female reproductive structure (the pistil) of a flower in angiosperms or to the ovule in gymnosperms
self-pollination
the transfer of pollen grains from an anther to the stigma of the same flower or to the stigma of another flower on the same plant
cross-pollination
a reproductive process in which pollen from one plant is transferred to the stigma of another plant
true-breeding
describes organisms or genotypes that are homozygous for a specific trait and thus always produce offspring that have the same phenotype for that trait
P generation
parental generation, the first two individuals that mate in a genetic cross
F1 generation
the first generation of offspring obtained from an experimental cross of two organisms
F2 generation
the second generation of offspring, obtained from an experimental cross of two organisms; the offspring of the F1 generation
dominant
in genetics, describes an allele that is fully expressed whenever the allele is present in an individual
recessive
in genetics, describes an allele that is expressed only when no dominant allele is present in an individual
law of segregation
states that the pairs of homologous chromosomes separate in meiosis so that only one chromosome from each pair is present in each gamete
law of independent assortment
the law that states that genes separate independently of one another in meiosis
allele
one of the alternative forms of a gene that governs a characteristic, such as hair color
genotype
the entire genetic makeup of an organism; also the combination of genes for one or more specific traits
phenotype
an organism’s appearance or other detectable characteristic that results from the organism’s genotype and the environment
homozygous
describes an individual that has identical alleles for a trait on both homologous chromosomes
heterozygous
describes an individual that has two different alleles for a trait
probability
the likelihood that a possible future event will occur in any given instance of the event
monohybrid cross
a cross between individuals that involves one pair of contrasting traits
Punnett square
a graphic used to predict the results of a genetic cross
genotypic ratio
the ratio of the genotypes that appear in offspring
phenotypic ratio
the ratio of phenotypes produced by a cross
test cross
the crossing of an individual of unknown genotype with a homozygous recessive individual to determine the unknown genotype
complete dominance
a relationship in which one allele is completely dominant over another
incomplete dominance
a condition in which a trait in an individual is intermediate between the phenotype of the individual’s two parents because the dominant allele is unable to express itself fully
codominance
a condition in which both alleles for a gene are fully expressed
dihybrid cross
a cross between individuals that have different alleles for the same gene
sex chromosome
one of the pair of chromosomes that determine the sex of an individual
autosome
any chromosome that is not a sex chromosome
sex-linked trait
a trait that is determined by a gene found on one of the sex chromosomes, such as the X chromosome or the Y chromosome in humans
linked gene
one of a pair of genes that tend to be inherited together
chromosome map
a diagram of gene positions on a chromosome
map unit
in chromosome mapping, an increment of 1 percent in the frequency of crossing-over
germ-cell mutation
mutation that occurs in an organism’s gametes
somatic-cell mutation
a mutation that occurs in a body cell
lethal mutation
a gene or chromosomal mutation that influences the development of an organism in such a way that the organism cannot survive
pedigree
a diagram that shows the occurrence of a genetic trait in several generations of a family
carrier
in biology, an individual who has one copy of a recessive autosomal allele that causes disease in the homozygous condition
genetic disorder
an inherited disease or disorder that is caused by a mutation in a gene or by a chromosomal defect
multiple alleles
more than two alleles (versions of the gene) for a genetic trait