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30 Cards in this Set
- Front
- Back
model organism
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-individuals are small, short-lived, inexpensive to care for, able to produce large numbers of offspring, and easy to manipulte experimentally
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Blending inheritance is wrong
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-Mendel's first cross of truebreeding round and wrinkle lines yields all round F1 progeny
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reciprocal cross
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for heterozygous-heterozygous cross, crossing male dominant w/female recessive and female dominant and male recessive to ensure no sex linkage of a trait
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theory of particulate inheritance
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hereditary determinants do not blend - they maintain their integrity from generation to generation
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gene
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hereditary determinant for a trait
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alleles
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different versions of the same gene
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genotype
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the alleles found in an individual
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principle of segregation
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-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 |
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monohybrid cross
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cross btwn male and female that are heterozygous at the gene in question (3:1 progeny)
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principle of independent assortment
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-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 |
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testcross
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-cross btwn individual with unknown genotype with truebreeding(homozygous), recessive individual
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locus
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where a gene is located
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chromosome theory of inheritance
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-Mendel's rules can be explained by the independent alignment and separation of homologous chromosomes at meiosis I
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wild type
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-individuals with the most common phenotype
-"w+" |
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mutation
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a change in a gene
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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 |
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linkage
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-genes found on the same chromosome
-should violate principle of independent assortment (doesn't always, do you know why?) |
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NOTATION
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writing genotype (listing relevant alleles that are present):
-use a / to separate homolouse alleles that are linked i.e. wy+/w+y |
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recombinant
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combination of alleles on in progeny that are different than combination of alleles found in parental generation
-result of crossing over |
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genetic mapping
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-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 |
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crossing over
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-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 |
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multiple allelism
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-more than two alleles for the same gene
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polymorphic
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-when more than two distinct phenotypes are present for a trait in a population due to multiple allelism
i.e. B-globin inhumans |
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incomplete dominance
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-heterozygotes have an intermediate phenotype
-1:2:1 genotype and phenotype i.e. lavender four-o'clocks |
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codominance
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-heterozygotes have the phenotype associated with both alleles present
-both alleles represented in phenotype |
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pleotropic
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-a gene that influences many traits, rather than just one
i.e. Marfan syndrome |
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epistasis
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-an allele of one gene masks the effect of an allele @ another gene
i.e. pepper color, chicken comb |
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discrete traits
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-characteristics that are qualitatively different
i.e.seed color is either yellow or green |
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quantitative traits
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-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) |
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polygenic inheritance
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-results in the transmission of quantitative traits
-each gene adds a small amount to the value of the phenotype |