Quantitative Trait Variation

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Quantitative Trait Variation 1

Variation in phenotype In addition to understanding genetic variation within at-risk systems, phenotype variation is also important. reproductive fitness traits related to the production of fertile offspring that survive to reproductive age. life history traits e.g. flowering time, reproductive age morphology disease resistance 2

Phenotypic Variation Which population has more variation? 3

The answer 4

For quantitative traits, we measure variation via Variance (s 2 ) 5

Variance (s 2 ) Character (pheno) must have numeric measurements. The value of s 2 depends on: 1. the measured outcomes possible for that character; 2. the probabilities of seeing those outcomes. 6

Variance (s 2 ): tossing a die Case 1: a fair die (all values equally likely) Outcome 1 1/6 2 1/6 3 1/6 4 1/6 5 1/6 6 1/6 probability Case 2: a loaded die (biased towards a given outcome) Outcome 1 1/10 2 1/10 3 1/10 4 1/10 5 1/10 6 1/2 probability s 2 = s 2 = 7

Variance (s 2 ): tossing a die Case 1: a fair die (all values equally likely) Outcome 1 1/6 2 1/6 3 1/6 4 1/6 5 1/6 6 1/6 probability Case 2: a loaded die (biased towards a given outcome) Outcome 1 1/10 2 1/10 3 1/10 4 1/10 5 1/10 6 1/2 probability s 2 = 2.91 s 2 = 3.25 8

Variance (s 2 ): tossing a die Case 1: a fair die (all values equally likely) Outcome 1 1/6 2 1/6 3 1/6 4 1/6 5 1/6 6 1/6 probability Case 3: high probability of extreme values Outcome 1 1/2 2 0 3 0 4 0 5 0 6 1/2 probability s 2 = s 2 = 9

Variance (s 2 ): tossing a die Case 1: a fair die (all values equally likely) Outcome 1 1/6 2 1/6 3 1/6 4 1/6 5 1/6 6 1/6 probability Case 3: high probability of extreme values Outcome 1 1/2 2 0 3 0 4 0 5 0 6 1/2 probability s 2 = 2.91 s 2 = 6.25 10

Variance (s 2 ) Variance is maximized when outcomes are at their two extremes low and high, with similar frequencies. not when the number of likely outcomes is large. diversity vs. high variance. 11

Variance Note that there is a difference between the model variance s 2 (we ll talk about this first) And an estimate of variance collect data; use it to calculate sample variance. (we ll talk about this second) 12

Partitioning variance Identifying sources of variance factors that are responsible for individuals looking different from one another. 13

Sources of Variance Factors that are responsible for individuals looking different from one another. Number of eyes on a Martian Male Martians # eyes probability 1 0.15 2 0.60 3 0.25 Female Martians # eyes probability 3 0.15 4 0.60 5 0.25 Variance among a male-only population; a female-only population; a mixed population 14

Factors that may affect variance in phenotype Genetic variability in populations Individuals are genetically different from one another. However not all genetic variation creates differences in phenotypes. Variation in environmental exposures Different individuals have experienced different environmental conditions. These differences also may or may not create differences in phenotypes. 15

Pheno variance and selection If individuals in a population are monomorphic for a given trait, selection cannot act on that trait. If there is variation in the trait, but individuals are genetically invariant at the loci that contribute to this trait, selection cannot act on the trait. 16

Pheno variance and selection For selection to act on a trait: 1. genetic variation must exist in the population; AND, 2. some variation in the trait must be due to genetic differences between individuals. 17

Pheno variance and selection How much of the variation in the trait is due to individuals in the population having different genotypes? 18

Pheno variance and selection How much of the variation in the trait is due to individuals in the population having different genotypes? Note: this is a different question than asking how many loci, or which loci, or are there loci at all, responsible for the development of the trait (e.g. is the trait genetic ) remember, if these loci exist, but everyone in the population carries the same alleles at these loci, then variation in this trait is not due to genetic differences (and selection cannot act on the trait). 19

Heritability A measure of how much of the population variance of a trait is due to individuals in the population having different genotypes

Variance of a phenotype that follows this distribution What happens to overall variance if males and females differ slightly? And to overall variance if they differ even more? Note that it s not enough just to have both males and females in the population they need to differ. And note that there s no effect on variance if males and females differ, but there are only males or only females in the population. 21

A genetic locus bb Bb If there are different genotypes present in the population, and, if they have different effects on the phenotype, BB This will create larger variance in phenotype than in a monomorphic population or than there would be if all genotypes had the same effect on phenotype. 22

Effect of genotypes on variance The question is: how much of the variance in phenotype can be explained by the presence of different genotypes in the population? Quantify how different individuals are because they have different genotypes. Total phenotype variance: s 2 P Phenotype variance that can be explained by individuals having different genotypes: s 2 G 23

Total phenotype variance, s 2 P m s 2 P = E [ (X - m) 2 ] 24

Genotypes with different effects on the phenotype m bb m Bb m BB m bb m Bb m BB Genotype values: mean phenotype for all individuals with that genotype 25

Genotypes with different effects on the phenotype m m bb m Bb m BB s 2 G = E[ (difference between the genotype values and the population mean) 2 ] genotype values: m bb m Bb m BB (mean phenotype for all individuals with that genotype) 26

Variance in phenotype caused by genetic variation: s 2 G s 2 G = E[ (difference between the genotype values and the population mean) 2 ] s 2 G = E [ (X - m) 2 ] = p 2 B (m BB - m) 2 + 2p B p b (m Bb - m) 2 + p 2 b (m bb - m) 2 27

Broad sense heritability, H 2 s 2 P : variance in phenotype measures how different individuals are from one another for any reason. s 2 G : variance in phenotype measures how different individuals are from one another because they have different genotypes. s 2 G s 2 P because s 2 G is probably only one part of s 2 P. H 2 = s 2 G / s 2 P 28

s 2 P : variance in phenotype measures how different individuals are from one another for any reason. s 2 G : variance in phenotype measures how different individuals are from one another because they have different genotypes. s 2 E : variance in phenotype measures how different individuals are from one another because they have experienced different environmental exposures. H 2 = σ G 2 σ P 2 = σ 2 G σ 2 G +σ2 E 29

Broad sense heritability, H 2 Of all the phenotypic variance in the population, what proportion of it is because individuals have different genotypes. m bb m Bb m BB Aa BB Aa bb AA bb Aa AA Bb BB AA Bb aa aa BB Bb aa bb 30

Heritability Proportion of phenotypic variance that can be explained by variation in genotypes. Depends on allele frequencies. Varies from population to population. different allele frequencies. different environmental conditions. Varies over time within a population. changing allele frequencies. changing environmental conditions. 31

Narrow sense heritability, h 2 To understand h 2, you need to understand additive genetic variance s 2 A ( A for additive) phenotype variance that can be inherited from one generation to the next. Can be predicted for offspring based on parents. To understand s 2 A, it s helpful to understand additive effects of alleles a i ( i for allele i) 32

Additive effects of alleles Phenotypic values associated with alleles. Theoretical constructs (alleles themselves don t have phenotypes) Needed because individuals don t pass along their genotypes to their offspring, they pass along their alleles. The pheno component that is inherited from a parent to an offspring is connected to the values of alleles. 33

Additive effects of alleles a B = E [phenotype for all BB and Bb indivs] m. How much do individuals who carry at least one B allele differ from the overall population mean? a B = p B m BB + p b m Bb m. depends on allele frequencies. 34

s 2 A : Additive genetic variance s 2 A = p 2 B (2a B ) 2 + 2p B p b (a B + a b ) 2 + p 2 b (2a b ) 2 [lots of algebra] s 2 A = p B a B2 + p b a b 2 [more algebra] s 2 A = 2p B p b a 2 a = additive effect of allele substitution (a B a b ) 35

Narrow-sense heritability: h 2 h 2 = s 2 A / s 2 P Of all the variance in phenotype in the population, what proportion of it is explained by the effects of the alleles that are segregating in the population. Explains what proportion of variance in phenotype can be inherited from one generation to the next Because alleles are transmitted from one generation to the next, not genotypes. 36

Estimating heritability If one of the reasons individuals look different from each other in a population is because individuals are genetically different (meaning genetic variation is a source of phenotype variation) Then, groups of individuals who are more genetically similar to each other (relatives) should also be more phenotypically similar. 37

Flipping this around If relatives resemble each other more than unrelated individuals do then this is an indication that some of the variation in phenotype in the population is due to genetic variation in the population. which indicates that heritability is greater than zero. Use this to estimate heritability. 38

Estimating h 2 : parent-offspring We know a parent shares one allele with its offspring IBD (at each locus). If offspring resemble their parents more closely than offspring resemble random individuals tall parents have tall offspring short parents have short offspring then allelic variation segregating in the population contributes to pheno var. 39

Estimating h 2 : parent-offspring Offspring don t resemble their parents more closely than they resemble unrelated individuals. Individuals may look different from each other, but not because of genetic differences. Allelic variation does not contribute to pheno variance. heritability is low to zero. Offspring s phenotypes are correlated with their parents phenotypes. One of the reasons individuals look different from one another is because of genetic differences. Allelic variation is contributing to pheno variance. heritability is high. 40

Narrow-sense heritability: h 2 It is the measure that predicts how well a trait responds to selection. Fitness traits: high selection pressure. Expectation that h 2 will generally be low for traits associated with fitness. 41

Estimating h 2 of fitness traits: Bottlenose dolphins 42

h 2 estimate of a fitness trait Female calving success: #offspring surviving to age 3 #of years reproductive data was available Free-living dolphin population Shark Bay, Western Australia extensively studied since 1980s Found that h 2 = 0.162. 16.2% of variation in calving success can be explained by allelic variation in the population. correlation between calving success rates of related individuals. Frère, et al. (2010) PNAS 107(46):19949 19954. 43

Other factors affecting variation in calving success in this population Social parameters: social transmission of information The fitness of social learners can be dependent upon the individuals from whom they learn who may not be relatives Found that 44% of variation in calving success can be explained by variation in social group membership correlation between calving success rates of unrelated members within social groups. 44

Factors affecting variation in calving success in this population h 2 > 0 There is the potential for selection to act on this trait directly. Variation in social group memberships is also an important factor explaining variation in calving success. Selection for social group membership (behavior traits) may be much less effective and/or slower. 45

Quantitative trait variation in fragmented populations Remember the consequences for genetic variation in fragmented populations 46

gen 0 gen 1 gen 2 gen G Early in the process (before much time has passed after fragmentation), the subpopulations genetic composition will be similar to each other. Allele frequencies will be similar (variance will be low). 47

gen 0 gen 1 gen 2 gen G Later in the process, genetic variation will start to be lost within the individual subpopulations. Which alleles become rarer in each subpopulation is random. Variation in p gets larger. 48

Quantitative trait variation in fragmented populations Alleles underlying quantitative trait variation are also undergoing drift. Allele frequencies increasing/decreasing. Genetic variation is being lost within subpopulations. Variance in phenotype (s 2 G) is being lost within subpopulations relative to the total population. 49

Quantitative trait variation in fragmented populations Alleles underlying quantitative trait variation are undergoing drift. Selection for fitness traits is also potentially occurring. Selection pressures may be similar across subpopulations. Or different pressures may exist for different subpopulations. driving differences between them. 50

Quantitative trait variation in fragmented populations Q ST measures quantitative trait differentiation between subpopulations. Q ST = σ B 2 σ B 2 +σ W 2 σ B 2 = variance in phenotype explained by differences between subpopulations. σ W 2 = variance in phenotype of individuals (or families) within subpopulations. 51

Quantitative trait variation in fragmented populations Q ST measures quantitative trait differentiation between subpopulations. Measures how much variance in phenotype can be explained by individuals being members of different subpopulations. 52

Q ST and F ST These parameters have been shown to be equivalent under neutral subdivided population models: Drift is the only force affecting allele frequencies. If Q ST F ST, this could be a signature of selection. Stabilizing selection: Q ST < F ST Diversifying selection: Q ST > F ST 53

Psilopeganum sinense 54

Psilopeganum sinense Historically rare, now endangered. endemic to the Yangtze River valley south-central China Seven populations; five traits Q ST not statistically different from F ST for two traits Q ST < F ST for three traits. Trait variation differentiation of these subpopulations appears to be neutral. Ye, et al. (2014) Annals of Botany 113:79 86. 55

great snipe (Gallinago media) 56

great snipe (Gallinago media) Two habitat regions: Scandinavia and Eastern Europe. Scandinavia is host to a small population. Historically, these two regions were more closely, if not completely, connected. Up to the mid-19th century, habitat also included large parts of the lowlands of western Europe now extinct in W. Europe Currently classified as Near Threatened at a global level. 57 Sæther, et al. (2007) European Society for Evolutionary Biology 20:1563 1576.

great snipe (Gallinago media) Samples were taken from seven sites in Norway, one site in Poland, and two sites in Estonia. F ST values between pairs of populations were small-moderate (max F=0.090). Six traits were measured For two, Q ST > F ST across regions, and small (ns) differences within regions. Concluded that neutral genetic differentiation was not sufficient to explain geographic differentiation (divergent selection) 58

Narrow sense heritability Some of the technical details 59

Additive effects of alleles: a i a i = E [phenotype for all individuals who carry allele i] m Consider a locus with two alleles, B and b Three genotypes: BB, Bb, bb a B = E [pheno for all BB and Bb indivs] m (BB and Bb individuals as a single group) a b = E [pheno for all Bb and bb indivs] m 60

Additive effects of alleles a B = E [phenotype for all BB and Bb indivs] m. How much do individuals who carry at least one B allele differ from the overall population mean? a B = p B m BB + p b m Bb m. depends on allele frequencies If the b allele is rare, then there will be a lot more BB individuals than Bb which affects the mean phenotype of the group of BB and Bb individuals. 61

Genotype values & additive effects What if all you knew about a phenotype were the additive effects of alleles? (for all alleles affecting the trait; let s assume one locus, two alleles for now) Could you describe the genotype values in terms of the additive effects of alleles? m BB = m + a B + a B = m + 2a B m Bb = m + a B + a b m bb = m + a b + a b = m + 2a b Is this reasonable? Would it be perfect? 62

phenotype Genotype values (m BB, m Bb, m bb ) m bb m BB m Bb BB Bb bb 63

phenotype Genotype values predicted from additive effects m + a B + a b m + 2a b m + 2a B BB Bb bb 64

phenotype Genotype values predicted from additive effects m + a B + a b m + 2a b m + 2a B BB Bb bb 65

phenotype Dominance deviations d bb d Bb d BB BB Bb bb 66

phenotype Genotype values predicted from additive effects m + a B + a b m + 2a b m + 2a B BB Bb bb 67

phenotype s 2 G : variance in phenotype due to variation in genotype variance created by these values BB Bb bb 68

phenotype s 2 A : Additive genetic variance variance created by these values s 2 A s 2 G s 2 P BB Bb bb 69

s 2 A : Additive genetic variance s 2 G = p 2 B (m BB - m) 2 + 2p B p b (m Bb - m) 2 + p 2 b (m bb - m) 2 s 2 A = E [ (X - m) 2 ] = p 2 B (m + 2a B m) 2 + 2p B p b (m + a B + a b m) 2 + p 2 b (m + 2a b m) 2 s 2 A = p 2 B (2a B ) 2 + 2p B p b (a B + a b ) 2 + p 2 b (2a b ) 2 70

s 2 A : Additive genetic variance s 2 A = p 2 B (2a B ) 2 + 2p B p b (a B + a b ) 2 + p 2 b (2a b ) 2 [lots of algebra] s 2 A = p B a B2 + p b a b 2 [more algebra] s 2 A = 2p B p b a 2 a = additive effect of allele substitution (a B a b ) 71

Narrow-sense heritability: h 2 h 2 = s 2 A / s 2 P Of all the variance in phenotype in the population, what proportion of it is explained by the additive effects of the different alleles that are segregating. what proportion of it can be inherited from one generation to the next can be predicted for offspring by knowing the parents. Because alleles are transmitted from one generation to the next, not genotypes. 72