Mendelian Genetics Flashcards
heredity
The transmission of traits from parents to offspring via genetic information.
model organism
An organism selected for intensive scientific study based on features that make it easy to work with (e.g., body size, life span), in the hope that findings will apply to other species.
pollen grains
In flowering plants, a male gametophyte enclosed within a protective coat.
pure line
In animal or plant breeding, a strain of individuals that produce offspring identical to themselves when self-pollinated or crossed to another member of the same population. Pure lines are homozygous for most, if not all, genetic loci.
F1 Generation
First filial generation. The first generation of offspring produced from a mating (i.e., the offspring of the parental generation).
monohybrid cross
A mating between two parents that are both heterozygous for a given gene.
When do the terms dominant and recessive apply to genetics?
When a distinct phenotype is shown when the individual carries two different genetic determinants for each trait.
reciprocal cross
A breeding experiment in which the mother’s and father’s phenotypes are the reverse of that examined in a previous breeding experiment.
particulate inheritance
The observation that genes from two parents do not blend together to form a new physical entity in offspring, but instead remain separate or particle-like.
dihybrid cross
A mating between two parents that are heterozygous for both of the two genes being studied.
principle of independent assortment
The concept that each pair of hereditary elements (alleles of the same gene) behaves independently of other genes during meiosis.
test cross
The breeding of an individual of unknown genotype with an individual having only recessive alleles for the traits of interest in order to infer the unknown genotype from the phenotypic ratios seen in offspring.
locus
A gene’s physical location on a chromosome.
Which genetic process is responsible for Mendel’s principle of segregation?
Anaphase Meiosis 1
chromosome theory of inheritance
The principle that genes are located on chromosomes and that patterns of inheritance are determined by the behavior of chromosomes during meiosis.
wild type
The most common phenotype seen in a population; especially the most common phenotype in wild populations compared with inbred strains of the same species.
mutation
Any change in the hereditary material of an organism (DNA in most organisms, RNA in some viruses).
x-linked inheritance
Inheritance patterns for genes located on the mammalian X chromosome. Also called X-linkage.
y-linked inheritance
Inheritance patterns for genes located on the mammalian Y chromosome. Also called Y-linkage.
sex-linked inheritance
Inheritance patterns observed in genes carried on sex chromosomes, so females and males have different numbers of alleles of a gene and may pass its trait only to one sex of offspring. Also called sex-linkage.
autosomal inheritance
The inheritance patterns that occur when genes are located on autosomes rather than on sex chromosomes.
linkage
In genetics, a physical association between two genes because they are on the same chromosome; the inheritance patterns resulting from this association.
recombinant
Possessing a new combination of alleles. May refer to a single chromosome or DNA molecule, or to an entire organism.
genetic map
An ordered list of genes on a chromosome that indicates their relative distances from each other. Also called a linkage map or meiotic map.