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Assortative mating (Falconer & Mackay: chapter 10)

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

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Assortative mating (Falconer & Mackay: chapter 10)

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  1. Assortative mating(Falconer & Mackay: chapter 10) Sanja Franic VU University Amsterdam 2012

  2. ‘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?

  3. Plomin, R., DeFries, J.C., Roberts, M.K. (1977). Assortative mating by unwed biological parents of adopted children. Science, 196(4288), 449-450.

  4. degree of assortative mating: correlation r of the phenotypic values of the mated individuals

  5. 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

  6. 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

  7. 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)

  8. 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)

  9. 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)

  10. 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

  11. Primary genetic or primary environmental resemblance of mates:

  12. Primary genetic or primary environmental resemblance of mates: • occurs e.g. in groups that are genetically or environmentallly differentiated from each other

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. the correlation m between the breeding values causes an increase of the additive genetic variance, and consequently of the heritability • why?

  19. 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)

  20. 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

  21. 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)

  22. 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

  23. By how much is h2 increased?

  24. Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • h2n = .67 n

  25. Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .5 • h2n = .75 n

  26. Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .6 • h2n = .875 n

  27. 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

  28. Change in variance components under assortative mating: • VA0 = .5 • VP0 = 1 • → h20 = .5 • m = .4 • Dh2 = .17 n

  29. Change in variance components under assortative mating: • VA0 = .6 • VP0 = 1 • → h20 = .6 • m = .4 • Dh2 = .16 n

  30. Change in variance components under assortative mating: • VA0 = .7 • VP0 = 1 • → h20 = .7 • m = .4 • Dh2 = .14 n

  31. 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

  32. Questions?

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