Abstract

The major histocompatibility complex (MHC) of immunity genes has been reported to influence mate choice in vertebrates, and a recent study presented genetic evidence for this effect in humans. Specifically, greater dissimilarity at the MHC locus was reported for European-American mates (parents in HapMap Phase 2 trios) than for non-mates. Here we show that the results depend on a few extreme data points, are not robust to conservative changes in the analysis procedure, and cannot be reproduced in an equivalent but independent set of European-American mates. Although some evidence suggests an avoidance of extreme MHC similarity between mates, rather than a preference for dissimilarity, limited sample sizes preclude a rigorous investigation. In summary, fine-scale molecular-genetic data do not conclusively support the hypothesis that mate selection in humans is influenced by the MHC locus.

Highlights

  • The major histocompatibility complex (MHC) locus contains genes central to acquired immunity, as well as numerous olfactory receptors [1]

  • There is evidence in numerous species that genes involved in immunity influence mate choice

  • We conclude that HapMap samples do not conclusively support the hypothesis that MHC genotypes exert an influence on mate choice

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Summary

Introduction

The MHC locus contains genes central to acquired immunity, as well as numerous olfactory receptors [1]. It is reported to influence mate selection in a number of vertebrates, and is thought to act through the sense of smell to favor genetic dissimilarity between parents and heterozygosity in offspring [2]. Evidence for these effects in humans includes the high degree of MHC polymorphism [1], MHC-dependent female sexual interest [3] and preferences for male body odors [4,5,6], and a depletion of matching five-locus HLA haplotypes in Hutterite couples [7]. The relationship of odor preference in these controlled settings to the selection of actual mates in practice is unclear

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