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. 2019 Mar 27;286(1899):20182664.
doi: 10.1098/rspb.2018.2664.

Genomic evidence for MHC disassortative mating in humans

Affiliations

Genomic evidence for MHC disassortative mating in humans

Claire Dandine-Roulland et al. Proc Biol Sci. .

Abstract

Although pervasive in many animal species, the evidence for major histocompatibility complex (MHC) disassortative mating in humans remains inconsistent across studies. Here, to revisit this issue, we analyse dense genotype data for 883 European and Middle Eastern couples. To distinguish MHC-specific effects from socio-cultural confounders, the pattern of relatedness between spouses in the MHC region is compared to the rest of the genome. Couples from Israel exhibit no significant pattern of relatedness across the MHC region, whereas across the genome, they are more similar than random pairs of individuals, which may reflect social homogamy and/or cousin marriages. On the other hand, couples from The Netherlands and more generally from Northern Europe are significantly more MHC-dissimilar than random pairs of individuals, and this pattern of dissimilarity is extreme when compared with the rest of the genome. Our findings support the hypothesis that the MHC influences mate choice in humans in a context-dependent way: MHC-driven preferences may exist in all populations but, in some populations, social constraints over mate choice may reduce the ability of individuals to rely on such biological cues when choosing their mates.

Keywords: GAIN-ADHD; MHC; mate choice; sexual selection.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1.
Figure 1.
Distribution of mean Rousset relatedness coefficient computed at the MHC level for real spouses (red line) and for permuted spouses (blue distribution, 105 permutations).
Figure 2.
Figure 2.
Mean Rousset relatedness coefficient between spouses across 3.6 Mb sliding windows (in increments of 300 kb) throughout the genome, plotted against the window recombination rate. The red point corresponds to the MHC.

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