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Assortative mating, described by Falconer and Mackay, highlights the tendency of individuals to pair with similar partners, as exemplified in human populations regarding stature and IQ. This phenomenon reflects a significant phenotypic correlation among mated individuals, challenging traditional heritability estimates. The degree of assortative mating, indicated by the correlation of phenotypic values, influences genetic consequences, determined by the underlying mating preferences—be they phenotypic, genetic, or environmental. This discussion also explores its applications in breeding programs and societal mating patterns.
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Assortative mating(Falconer & Mackay: chapter 10) Sanja Franic VU University Amsterdam 2012
‘like with like’ • reflected in a phenotypic correlation between mated individuals • mating in human populations is assortative with respect to many characteristics, such as stature and IQ • how does assortative mating affect the estimation of heritability?
Plomin, R., DeFries, J.C., Roberts, M.K. (1977). Assortative mating by unwed biological parents of adopted children. Science, 196(4288), 449-450.
degree of assortative mating: correlation r of the phenotypic values of the mated individuals
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates • r: observed, m: not
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates • r: observed, m: not • the relationship between r and m depends on what governs the choice of mates (phenotypic, genetic, or environmental resemblance)
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates • r: observed, m: not • the relationship between r and m depends on what governs the choice of mates (phenotypic, genetic, or environmental resemblance) • primary phenotypic resemblance: m = rh2 • (h2 = heritability of the character with respect to which the mates are chosen)
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates • r: observed, m: not • the relationship between r and m depends on what governs the choice of mates (phenotypic, genetic, or environmental resemblance) • primary phenotypic resemblance: m = rh2 • (h2 = heritability of the character with respect to which the mates are chosen) • this is how assortative mating is applied in breeding programmes (but NB: in man, assortative mating probably seldomly arises only in this way)
degree of assortative mating: correlation r of the phenotypic values of the mated individuals • the genetic consequences, however, depend on the correlation m between the breeding values of the mates • r: observed, m: not • the relationship between r and m depends on what governs the choice of mates (phenotypic, genetic, or environmental resemblance) • primary phenotypic resemblance: m = rh2 • (h2 = heritability of the character with respect to which the mates are chosen) • this is how assortative mating is applied in breeding programmes (but NB: in man, assortative mating probably seldomly arises only in this way) • the consequences to be described are restricted to primary phenotypic resemblance as cause of assortative mating
Primary genetic or primary environmental resemblance of mates:
Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other
Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other • this is probably how much of assort. mating in man arises
Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other • this is probably how much of assort. mating in man arises • e.g., SES groups as environmentally differentiated groups: • environment within each group is relatively homogenous with respect to SES • → mates within each group are more similar on SES to each other than to rest of the population
Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other • this is probably how much of assort. mating in man arises • e.g., SES groups as environmentally differentiated groups: • environment within each group is relatively homogenous with respect to SES • → mates within each group are more similar on SES to each other than to rest of the population • if primary correlation is wholly environmental (m = 0) → no genetic consequences of assortative mating
Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other • this is probably how much of assort. mating in man arises • e.g., SES groups as environmentally differentiated groups: • environment within each group is relatively homogenous with respect to SES • → mates within each group are more similar on SES to each other than to rest of the population • if primary correlation is wholly environmental (m = 0) → no genetic consequences of assortative mating • environmental correlation may be the basis of assortative mating on IQ in man • Rao, Morton, & Yee, 1976: • r = .5 explained by people choosing a spouse with a similar family background
Primary phenotypic resemblance of mates: m = rh2 • covA1A2 = cov(h2P1, h2P2) • = h4cov(P1,P2) • = h4rVP (because r=cov/V → cov=rV) • = h4rVA/h2 (because h2=VA/VP→ VP=VA/h2) • = rh2VA • covA1A2 = mVA (because m=covA1A2/VA) • so that: • rh2VA = mVA • m = rh2
the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why?
the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why? because an increased covariance within groups implies an increased variance between groups • (last lecture)
the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why? because an increased covariance within groups implies an increased variance between groups • (last lecture) • the correlations between relatives, however, are increased by more than one would expect from increased heritability alone
the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why? because an increased covariance within groups implies an increased variance between groups • (last lecture) • the correlations between relatives, however, are increased by more than one would expect from increased heritability alone • therefore, 2 meanings of h2 under assortative mating: • determination of the resemblance betwen relatives (eq. 10.5: h2 = b/r or t/r) • ratio of variance components (VA/VP)
the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why? because an increased covariance within groups implies an increased variance between groups • (last lecture) • the correlations between relatives, however, are increased by more than one would expect from increased heritability alone • therefore, 2 meanings of h2 under assortative mating: • determination of the resemblance betwen relatives (eq. 10.5: h2 = b/r or t/r) • ratio of variance components (VA/VP) • the two are not the same under assortative mating! • here, we retain the latter definition
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • h2n = .67 n
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .5 • h2n = .75 n
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .6 • h2n = .875 n
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .5 • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .6 • h2n = .67 • h2n = .75 • h2n = .875
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • Dh2 = .17 n
Change in variance components under assortative mating: • VA0 = .6 • VP0 = 1 • → h20 = .6 • m = .4 • Dh2 = .16 n
Change in variance components under assortative mating: • VA0 = .7 • VP0 = 1 • → h20 = .7 • m = .4 • Dh2 = .14 n
Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • VA0 = .6 • VP0 = 1 • → h20 = .6 • m = .4 • VA0 = .7 • VP0 = 1 • → h20 = .7 • m = .4 • Dh2 = .17 • Dh2 = .16 • Dh2 = .14