population genetics Flashcards

(39 cards)

1
Q

study of genetic variation in traits

A

quantitative genetics

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2
Q

foundation of evolutionary genetics

A

population + quantitative genetics
variation due to evolutionary history (processes shape variation)
to understand we require mathematical models

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3
Q

what creates variation at each locus

A

mutationw

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4
Q

what shuffles combination across loci among individuals

A

recombination

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5
Q

what is molecular genetic variation

A

varying DNA sequences among individuals

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6
Q

alleles

A

alternative DNA sequences ta locus
sequence of DNA inherited as a unit

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7
Q

loci

A

position in the genome of an allele

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8
Q

what do population, quantitative and evolutionary genetics all rely on

A

understanding concept of alleles and allele frequencies

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9
Q

SNP

A

single nucleotide polymorphism
(but sequences can differ in several ways or have complete structural differences)

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10
Q

what creates phenotypic differences

A

sequence differences
allelic variation

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11
Q

when all individuals have the same allele, a locus cannot contribute variation

A

only contributes when there are alternative alleles
depends on specific allelic variants at the locus

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12
Q

can you describe effect of gene

A

no
we can only describe phenotypic differences associated with different versions of the gene

genes with different alleles leading to different phenotypes produce genetically based phenotypic variation

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13
Q

how do allele frequencies relate to phenotypic variation

A

depends on frequencies of alleles

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14
Q

frequency of A

A

number of A alleles/ total number of alleles

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15
Q

frequency of a

A

number of a alleles/ total number of alleles

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16
Q

how many alleles in a diploid population of N individuals

17
Q

total number of A alleles in a diploid population

A

2x the number of AA homozygotes (nAA) + THE NUMBER OF Aa HETEROZYGOTES (nAa)

18
Q

so frequency of F(A)

A

2x(nAA) + (nAa)/ 2N= p
2x(naa) + (nAa)/ 2N=q

19
Q

why’s change in allele frequency important

A

tells us about evolutionary change

20
Q

how can population differences be used

A

to understand migration/ gene flow
different alleles favoured in different environments

21
Q

how do we measure genotype frequency

A

The proportion of a population with a given genotype.

22
Q

what is a hardy Weinberg model

A

A simple model where diploid individuals are constructed by randomly and independently sampling two alleles from an infinitely large pool of gametes.

23
Q

assumptions of hardy Weinberg model

A
  • Population infinitely large
    • Random mating- all individuals have an equal chance of mating with each other
    • No migration in or out of the population
    • No selection*
      No mutation*
24
Q

population very large means

A

no sampling error
allele frequencies constant

25
random mating means
all individuals equally as likely to mate with eachother no inbreeding, no outbreeding sampling of two alleles is independent
26
no migration means
closed pop. alleles not influenced by variation from other populations entering
27
no selection
genotypes have no effect on fitness all genotypes have same average survival and fecundity
28
no mutations
no new alleles enter no current alleles removed
29
why is HW idealised
assumptions always violated but pop is always close to HWE offers a null model, so we can ask why it is different, what rules were violated
30
prediction of HWE
allele frequency do not change as long as pop. meets assumptions genetic frequencies are product of alleles frequencies and will return to these frequencies after a single generation of random mating
31
what are alleles when they are rare
almost always heterozygotes mutations effect in heterozygote governs its initial fate (strongly impacts evolutionary processes)
32
non random mating
some allele combinations will occur at higher frequencies than expected or at lower frequencies
33
assortative mating
phenotype biased mating means frequencies of certain genotypes will be altered
34
positive assortative mating
individuals with similar traits more likely to mate with eachother
35
inbred
two alleles can be copies of the same allele in one of their ancestors, two alleles are IBD (from common ancestor)
36
inbreeding
matings tend to be between relatives relatives more likely to share allele beyond expected random chance increased levels of homozygosity
37
inbreeding coefficient f
probability that two alleles are IBD proportional reduction in heterozygosity compared to what is expected in HWE
38
inbreeding depression
when inbreeding reduces viability or fecundity homozygotes have lower fitness (caused by deleterious recessive mutations) which are hidden in heterozygotes and cannot be removed
39
genetic load
harboured deleterious recessive alleles across genome reflects mutation selection balance