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Types of biological variation Discontinuous (qualitative) variation : simple alternative forms; alternative phenotypes ; usually due to alternative genotypes often due to interactions of dominant and recessive alleles of genes common alternatives due to polymorphism
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Types of biological variation • Discontinuous (qualitative) variation: simple alternative • forms; alternative phenotypes; usually due to alternative • genotypes • often due to interactions of dominant and recessive • alleles of genes • common alternatives due to polymorphism • rare alternatives due to mutation (vs. wild type) • Continuously variable (quantitative) traits: no distinct increments; most common variation; due to polygenes • and/or significant non-genetic influence.
Development that is genetically driven Fig. 1-17
Development that is driven by interactions between genes and the environment Fig. 1-19
Norm of reaction: phenotypic outcome of the interactions of genotype and environment; characteristic for each genotype Developmental noise: random influences on phenotype that result in random individual variations
Drosophila melanogaster (wild-type) Fig. 1-20
Development resulting from interactions between genes, environment and “noise” Fig. 1-23
Chapter 2 Overview Fig. 2-1
Simple monohybrid inheritance • single gene (allele pair) • simple dominance of one allele
Mendel’s explanation of simple monohybrid inheritance • Genes are particulate • 2. Genes in pairs and can be • different forms (alleles) • 3. Halving of pairs in gametogenesis • 4. Alleles separate (segregate) in • gametogenesis • 5. Fertilization is random Fig. 2-7
Testcross to test/demonstrate heterozygosity Testcross: cross possible heterozygote to homozygous recessive Fig. 2-8
Dihybrid inheritance Fig. 2-10
Dihybrid inheritance Fig. 2-11
Estimating the likelihoods of events • Independent events: • Compute the likelihood of each event • Compute the product of those likelihoods • Dependent (mutually exclusive) events: • Compute the likelihood of each event • Compute the sum of those likelihoods
Problem: predict the phenotypic ratios expected among the progeny of the cross A/a ; b/b X A/a ; B/b Solution: use a branch diagram
Dihybrid inheritance Fig. 2-11
Problem: predict the phenotypic ratios expected among the progeny of the cross A/a ; b/b X A/a ; B/b Solution: use a branch diagram p. 155
Analysis of a rare autosomal, recessive phenotype Typical: affected males and females; affected individuals have unaffected parents Fig. 2-13
Analysis of a autosomal dominant phenotype Typical: affected males and females; about half of progeny of affected individual are affected Fig. 2-16
T.H. Morgan’s analysis of the sex linkage of white Fig. 2-24
Repeat from previous slide Fig. 2-24
Analysis of a rare sex-linked, recessive phenotype Typical: almost exclusively affected males; mothers of affected sons are carriers; appears to “skip” generations Fig. 2-25
Mirabilis jalapa Fig. 2-30
X2 (Chi-square) test: assesses the likelihood that a deviation from expectations can be accepted Example: Do results of a dihybrid cross reflect linkage? Products of a dihybrid (A/a B/b) testcross AB 142 ab 133 Ab 113 aB 112 Parental types Recombinant types
X2 (Chi-square) test: assesses the likelihood that a deviation from expectations can be accepted Example: Do results of a dihybrid cross reflect linkage? 1st step: Make “null hypothesis” – genes are not linked Predicts 1:1:1:1 ratio of gamete genotypes 2nd step: Compute X2 = (O-E)2 / E 3rd step: Determine degrees of freedom (number of independent measurements) 4th step: Consult X2 chart of critical values