Reduced reproductive success is associated with selective constraint on human genes

Eugene J. Gardner, Matthew D. C. Neville, Kaitlin E. Samocha, Kieron Barclay, Martin Kolk, Mari E. K. Niemi, George Kirov, Hilary C. Martin and Matthew E. Hurles ()
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Eugene J. Gardner: Wellcome Genome Campus
Matthew D. C. Neville: Wellcome Genome Campus
Kaitlin E. Samocha: Wellcome Genome Campus
Kieron Barclay: Max Planck Institute for Demographic Research
Martin Kolk: Stockholm University
Mari E. K. Niemi: Wellcome Genome Campus
George Kirov: Cardiff University
Hilary C. Martin: Wellcome Genome Campus
Matthew E. Hurles: Wellcome Genome Campus

Nature, 2022, vol. 603, issue 7903, 858-863

Abstract: Abstract Genome-wide sequencing of human populations has revealed substantial variation among genes in the intensity of purifying selection acting on damaging genetic variants1. Although genes under the strongest selective constraint are highly enriched for associations with Mendelian disorders, most of these genes are not associated with disease and therefore the nature of the selection acting on them is not known2. Here we show that genetic variants that damage these genes are associated with markedly reduced reproductive success, primarily owing to increased childlessness, with a stronger effect in males than in females. We present evidence that increased childlessness is probably mediated by genetically associated cognitive and behavioural traits, which may mean that male carriers are less likely to find reproductive partners. This reduction in reproductive success may account for 20% of purifying selection against heterozygous variants that ablate protein-coding genes. Although this genetic association may only account for a very minor fraction of the overall likelihood of being childless (less than 1%), especially when compared to more influential sociodemographic factors, it may influence how genes evolve over time.

Date: 2022
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DOI: 10.1038/s41586-022-04549-9

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