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30 Cards in this Set

  • Front
  • Back
model organism
-individuals are small, short-lived, inexpensive to care for, able to produce large numbers of offspring, and easy to manipulte experimentally
Blending inheritance is wrong
-Mendel's first cross of truebreeding round and wrinkle lines yields all round F1 progeny
reciprocal cross
for heterozygous-heterozygous cross, crossing male dominant w/female recessive and female dominant and male recessive to ensure no sex linkage of a trait
theory of particulate inheritance
hereditary determinants do not blend - they maintain their integrity from generation to generation
gene
hereditary determinant for a trait
alleles
different versions of the same gene
genotype
the alleles found in an individual
principle of segregation
-to explain Mendel's F2 3:1 ratio, alleles must segregate into the different gamete cells during the formation of eggs and sperm
-each gamete carries only one allele for a particular gene (wrinkle/round), because alleles have segregated during meiosis
monohybrid cross
cross btwn male and female that are heterozygous at the gene in question (3:1 progeny)
principle of independent assortment
-alleles from different genes are transmitted independently from one another (for genes located on different chromosomes)
-different genes assort independently because they are located on different chromosomes
testcross
-cross btwn individual with unknown genotype with truebreeding(homozygous), recessive individual
locus
where a gene is located
chromosome theory of inheritance
-Mendel's rules can be explained by the independent alignment and separation of homologous chromosomes at meiosis I
wild type
-individuals with the most common phenotype
-"w+"
mutation
a change in a gene
X-linked inheritance
(X-linkage)
-a gene that resides on a the X-chromosome, where the Y-chromosome does not carry an allele for that gene
-the discover of X-linked inheritance convinced most biologists that the chromosome theory of inheritance was correct
linkage
-genes found on the same chromosome
-should violate principle of independent assortment (doesn't always, do you know why?)
NOTATION
writing genotype (listing relevant alleles that are present):
-use a / to separate homolouse alleles that are linked
i.e. wy+/w+y
recombinant
combination of alleles on in progeny that are different than combination of alleles found in parental generation
-result of crossing over
genetic mapping
-diagram that shows the relative positions of genes along a particular chromosome
-found by looking at frequency of genetic recombinants
-19% recombinant progeny = 19 map units apart for genes
crossing over
-the farther apart two genes are on a chromosome, the more of a chance there is that crossing over will occur
-breaks up linkage and makes it appear as if independent assortment is occuring
-genes behave as if independently assorted when more than 50 or more map units apart
multiple allelism
-more than two alleles for the same gene
polymorphic
-when more than two distinct phenotypes are present for a trait in a population due to multiple allelism
i.e. B-globin inhumans
incomplete dominance
-heterozygotes have an intermediate phenotype
-1:2:1 genotype and phenotype
i.e. lavender four-o'clocks
codominance
-heterozygotes have the phenotype associated with both alleles present
-both alleles represented in phenotype
pleotropic
-a gene that influences many traits, rather than just one
i.e. Marfan syndrome
epistasis
-an allele of one gene masks the effect of an allele @ another gene
i.e. pepper color, chicken comb
discrete traits
-characteristics that are qualitatively different
i.e.seed color is either yellow or green
quantitative traits
-quantitative variation - individuals differ by degree
i.e.height/skin color
-when different values are plotted on a histogram (frequency distribution), they form a bell-shaped curve (normal curve)
polygenic inheritance
-results in the transmission of quantitative traits
-each gene adds a small amount to the value of the phenotype