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Population Genetics 6: Natural Selection Natural selection GENETIC SUCESS ⎯→ VARIATION + DIFFERENTI AL ⎯ This genetic prefix is important as the variation must be heritable. Change in this portion of the equation is undirected. (undirected) This has two components: (i) reproduction and (ii) survival in a particular environmental context. This portion provides a direction to evolutionary change EVOLUTION For this part of the course, we define evolution as change in allele frequencies (directed) Natural selection explains adaptation 1 Natural selection The conditions for natural selection: 1. variation among individuals (mutation) 2. replication (DNA, RNA, mitosis, meiosis) 3. inheritance (Mendelian transmission genetics) Fitness 2 Fitness: a measure of an organisms ability to survive and reproduce. Fitness may be measured in relation to viability (the probability of survival from fertilization to reproduction) and mean fertility. Relative fitness: measuring fitness by assigning a fitness value of 1 to the genotype with the highest absolute fitness. Selection coefficient (s): the difference between the relative fitness of the most fit genotype and the relative fitness of another involved genotype. Life is a struggle 3 Natural selection in action: HIV drug resistance HIV/AIDS: • 40 (±6million) million people worldwide (2006) • 33 (±3million) million people worldwide (2007) • 2 million are children (< age15); 90% in SubSaharan Africa • Two-thirds of infected people live in Africa Growth: • 2.7 million new infections in 2007 (3.0 in 2001) • >7,500 per day • 45% of new infections are young people (15-25) Toll: • > 20 million deaths since first case • 3 million deaths in 2006 • Death rate falling in developed countries since 1990’s Data from NIH, NIAID, UNAIDS [2008 report] 4 5 New statistic (Zimbabwe): Prior to HIV: Average lifespan = 60 years Current: Average lifespan = 36 years 6 HIV-1 genome: 7 Life cycle of HIV 8 Viral budding A billion viral particles are produced every day Fusion inhibitors: Inhibit the fusion of HIV with target cell membrane. Administered by injection Non-nucleoside RT inhibitors: Nucleoside RT inhibitors: The newest class of HIV drugs. The first effective class of antiretroviral drugs. Bind directly to reverse transcriptase and prevent synthesis of DNA from RNA template They mimic A,C,G or T. They incorporate themselves into growing DNA polymer and act to disrupt the replication complex. Protease inhibitors: These work at final stage of virus life cycle. They prevent proper assembly and release of mature HIV virus. Example: AZT 9 Natural selection in action: HIV drug resistance RT inhibitor treatment: 1. dramatic decline in HIV in patient 2. HIV grow to detectable numbers in a matter of days ⎯ completes life cycle in just 2 days 3. 1-2 months patient has 100% resistant population of HIV Resistance: 1. avoid incorporation of RT inhibitor 2. proofread and excise inhibitor Note: most resistant strains have lower fitness in untreated individuals. Compensatory mutations have been observed to evolve! 10 Concept map of evolution of resistance to RT inhibitors in HIV Generation: 1 2 3 4 No drugs 5 6 7 Single drug therapy High polymorphism Low resistance Low polymorphism High resistance Fitness in diploids Evolutionary fitness is symbolized with W Symbolism Genotype AA Aa aa Phenotype WAA WAa Waa 1 1 0.76 11 Fitness Directional selection 1 0.8 0.6 0.4 0.2 0 WAA > WAa > Waa AA Aa aa Genotypes Directional selection occurs when selection favors the phenotype at an extreme of the range of phenotypes. • exerts pressure for FIXATION (frequency goes to 1) • imposes a direction on evolution Overdominant selection 1 Fitness 0.8 WAA < WAa > Waa 0.6 0.4 0.2 0 AA Aa aa Genotypes Overdominant selection occurs when the heterozygote has a greater fitness than either homozygote. • also called balancing selection or heterozygote advantage • maintains a stable polymorphism; acts against fixation 12 Fitness Underdominant selection 1 0.8 0.6 0.4 0.2 0 WAA > WAa < Waa AA Aa aa Genotypes Underdominant selection occurs when the heterozygote has lower fitness than either homozygote. • yields an unstable equilibrium • also called apostatic selection or disruptive selection Fitness in diploids Genotype Frequency Phenotype Symbolism for generation 0 AA Aa 2 p0 2p0q0 WAA WAa aa 2 q0 Waa Survival ratio: WAA : WAa : Waa Genotype ratio: p2WAA : 2pqWAa : q2Waa Problem: the genotype ratios do not sum to 1. 13 Fitness in diploids Normalize by dividing by the grand total after selection: W = p2WAA + 2pqWAa + q2Waa W = AVERAGE FITNESS Normalized fitness: W W AA and Aa and Waa W W W p 2 + 2 pq + q 2 = 1 p2 W W AA + 2 pq Aa + q 2 Waa = 1 W W W Under HW: With selection: p1 = p2 + (1/2)2pq ( ) + (1/2)2pq ( ) WAA p1 = p2 W WAa W 14 Selection simplified… p1 = p(pWAA + qWAa) / W ⇐ Remember these. q1 = q(pWAa + qWaa) / W OK, now we have the tools we need… 1. Deleterious recessive 2. Deleterious dominant 3. Overdominant 4. Deleterious recessive under partial dominance Deleterious recessive 15 Deleterious recessive Our model Genotype AA Aa aa Frequency p 02 2p0q0 q 02 1 1 1-s W W = p2(1) + 2pq(1) + q2(1-S) We specify the fractional reduction in survival by the selection coefficient, s. (average fitness) W = p2 + 2pq + q2- Sq2 W = 1- q2S (average fitness, simplified) Deleterious recessive q1 = q(pWAa + qWaa) / W By substitution … q1 = q(p(1) + q(1- s)) / 1- sq2 q1 = q(p + q - sq) / 1- sq2 2 q1 = q(1 - sq) / 1- sq 2 qt+1 = qt - Sqt / 1- sqt 2 The per generation change in allele frequency due to selection against a deleterious recessive trait 16 Deleterious recessive Dark form Peppered moths in polluted environment Light form Genotype AA Aa Frequency at birth p2 2pq aa q2 Fitness 1 1 1-s Let p = 0.06 and q = 0.94 Change in recessive allele frequency over time (in generations) 1 Frequency of a allele Biston betularia: Dark allele (A) is dominant Light allele (a) is recessive In polluted environment, the light allele is deleterious 0.9 s = 0.33 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 One empirical estimate of s = 0.33 1 4 7 10 13 16 19 22 25 28 31 34 37 40 43 46 49 Generations Directional selection for dominant allele Deleterious recessive Change in recessive allele frequency over time under different intensities of negative selection 1 s=0 s = 0.01 Frequency of a allele 0.9 0.8 0.7 0.6 s = 0.1 s = 0.5 s = 0.9 0.5 0.4 0.3 0.2 0.1 0 1 26 51 s < 0.5 76 101 126 151 176 201 226 251 Generations 17 Deleterious dominant Fitness Recall: Directional selection 1 0.8 0.6 0.4 0.2 0 WAA > WAa > Waa AA Aa aa Genotypes Directional selection occurs when selection favors the phenotype at an extreme of the range of phenotypes. • exerts pressure for FIXATION (frequency goes to 1) • imposes a direction on evolution 18 Deleterious dominant Peppered moths in restored environment The model Genotype AA Aa aa Frequency p 02 2p0q0 q 02 1-s 1-s 1 W Biston betularia: Dark allele (A) is dominant Light allele (a) is recessive q − sq + sq 2 q1 = 1− s 1− q2 ( In clean environment, the dark allele is deleterious ) Directional selection for the recessive allele Deleterious dominant Change in frequency of dominant allele under different intensities of negative selection 1 Frequency of A allele 0.9 s = 0.05 s = 0.1 s = 0.2 s = 0.5 0.8 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 1 9 17 25 33 41 49 57 65 73 81 89 97 Generations Note: At one site in northwest England the frequency of the dark form of the Peppered Moth declined from 0.94 in 1961 to 0.11 in 1998. 19 Recall: Overdominant selection 1 Fitness 0.8 WAA < WAa > Waa 0.6 0.4 0.2 0 AA Aa aa Genotypes Overdominant selection occurs when the heterozygote has a greater fitness than either homozygote. • also called balancing selection or heterozygote advantage • maintains a stable polymorphism; acts against fixation 20 Overdominance (Balancing selection) The model AA Aa p 02 2p0q0 1 – s1 1 Genotype Frequency W q1 = aa q 02 1 – s2 q − s2 q 2 1 − s1 p 2 − s 2 q 2 Let s look at an example: s1 = 0.3 and s2 = 0.1 Overdominance (Balancing selection) Let s1 = 0.3 and s2 = 0.1 Stable equilibrium resulting from overdominant selection 1 Frequency of a allele 0.9 0.8 Stable polymorphism: q = 0.75 p = 0.25 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 1 7 13 19 25 31 37 43 49 55 61 67 73 79 85 91 97 Generations What happens to this polymorphism during speciation? 21 Overdominance (Balancing selection) MHC locus: Virus infected cell • Major histocompatibility locus Antigen presenting receptor • 4 mega-base region of the genome • Encodes antigen presenting receptor proteins TCR T Class I Class II Class III The MHC locus on human chromosome 6 Killer cell Overdominance (Balancing selection) ARS 22 MCHBh MCHAh MCHAch MCHBch Overdominance (Balancing selection) 6 mya: Human – chimp speciation 9 mya: MHCBh - MHCBch 14 mya:MHCAh - MHCAch Trans-species polymorphism ! Deleterious recessive under partial dominance The model Genotype AA Aa aa s = selection coefficient Frequency p 02 2p0q0 q 02 h = degree of dominance 1 1 - hs 1–s W h = 0 : dominance is 100%, recessives hide in heterozygotes h = ½: dominance is 50%, additive models for phenotypic effect q1 = q − hspq − sq 2 1 − 2hspq − sq 2 23 Deleterious recessive under partial dominance Effect of partial dominance on the change of the recessive allele frequency under negative selection 1 Frequency of a allele 0.9 Partial Dominance: h = 0.5 s = 0.33 0.8 0.7 0.6 0.5 Full Dominance: h=0 s = 0.33 0.4 0.3 0.2 0.1 0 1 4 7 10 13 16 19 22 25 28 31 34 37 40 43 46 49 52 55 58 Generations 24