M6 MacLean- Population Genetics of Adaptation I + II

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6 Terms

1
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what are the assumptions in the hardy-weinberg theorem and what does it state?

assumptions:

  • there is an infinite population size

  • mating is random

  • the genes of interest have no impact on fitness/do not have differences in viability

the hardy-weinberg theorem states that allele and genotype frequencies in a population will remain constant from generation to generation in the absence of other evolutionary influences eg. mutations, selection, or genetic drift

P² + 2PQ + Q² = 1

P + Q = 1

2
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how can the hardy-weinberg theorem be adapted to account for selection?

fitness (W) can be calculated- the relative reproductive rate of an individual with a given genotype (how likely the allele is to be inherited)

this is dependent on:

  • the selection coefficient (s)- whether the allele is more beneficial (positive coefficient) or more deleterious (negative coefficient) than Q

  • the dominance (h)- dominant = 1, recessive = 0

fitness is measured relative to Q, so Q = 1:

  • the fitness of P in P homozygous individuals (P²) is 1+s

  • the fitness of P in heterozygous individuals (2PQ) is 1+hs (accounts for whether it is dominant or recessive)

  • the fitness of P in Q homozygous individuals (Q²) is 0

if you add the fitnesses for the P allele and the Q allele (1), you get the average fitness (W) = P²(1+s) + 2PQ (1+hs) + Q²(1)

the frequency of the P allele in the next generation is P²(1+s)/W + PQ(1+hs)/W

3
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what is the graph of a beneficial allele frequency when it is introduced to a new population?

  • recessive beneficial alleles take longer to fix in a population because they can only show a beneficial effect when homozygous, which is rare at first

  • the frequency slowly increases at first, until some organisms are homozygous, where it causes a ‘selective sweep’ because that allele will then be greatly selected for

<ul><li><p><strong>recessive </strong>beneficial alleles take <strong>longer </strong>to <strong>fix </strong>in a population because they can only show a beneficial effect when <strong>homozygous</strong>, which is <strong>rare </strong>at first</p></li><li><p>the frequency <strong>slowly increases </strong>at first, until some organisms are homozygous, where it causes a ‘<strong>selective sweep</strong>’ because that allele will then be greatly selected for</p></li></ul><p></p>
4
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how can the hardy-weinberg theorem be adapted for an island model of structured populations?

the allele frequency in the next generation (on one island) is dependent on the migration rate (m)- the probability that the allele arrives on the island by migration

the frequency in the next generation (P2) = P1(1-m) + P* (m)

where P* = the average allele frequency on other islands

(the 1-m is because if there is migration of the allele onto the island, there is also migration of the allele off the island)

<p>the allele frequency in the next generation (on one island) is dependent on the <strong>migration rate (m)</strong>- the probability that the allele arrives on the island by migration</p><p><strong>the frequency in the next generation (P<sub>2</sub>) = P<sub>1</sub>(1-m) + P* (m)</strong></p><p>where P* = the average allele frequency on other islands</p><p>(the 1-m is because if there is migration of the allele onto the island, there is also migration of the allele off the island)</p>
5
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how does migration affect allele frequencies?

  • if there is gene flow between populations, they will all eventually reach an average allele frequency

  • the number of generations that this takes to occur is dependent on the rate of migration

<ul><li><p>if there is gene flow between populations, they will <strong>all </strong>eventually reach an <strong>average allele frequency</strong></p></li><li><p>the number of generations that this takes to occur is dependent on the <strong>rate </strong>of migration</p></li></ul><p></p>
6
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how does recombination affect adaptation?

  • recombination accelerates adaptation and evolution by bringing together beneficial mutations

  • without recombination (in a haploid population), two beneficial alleles would have to compete with each other, as they could never be inherited together

  • in the top diagram, without recombination, b and c are outcompeted by a, and ac is outcompeted by ab

  • in the bottom diagram, with recombination, evolution happens much faster because the beneficial mutations can combine

  • sexual reproduction creates much greater genetic diversity through recombination

<ul><li><p><strong>recombination accelerates adaptation</strong> and evolution by bringing together beneficial mutations</p></li><li><p><strong>without </strong>recombination (in a haploid population), two beneficial alleles would have to <strong>compete </strong>with each other, as they could never be inherited together</p></li><li><p>in the top diagram, without recombination, b and c are outcompeted by a, and ac is outcompeted by ab</p></li><li><p>in the bottom diagram, with recombination, evolution happens much faster because the beneficial mutations can combine</p></li><li><p><strong>sexual reproduction creates much greater genetic diversity through recombination</strong></p></li></ul><p></p>