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The DNA-binding protein PRDM9 directs positioning of the double-strand breaks (DSBs) that initiate meiotic recombination in mice and humans. Prdm9 is the only mammalian speciation gene yet identified and is responsible for sterility phenotypes in male hybrids of certain mouse subspecies. To investigate PRDM9 binding and its role in fertility and meiotic recombination, we humanized the DNA-binding domain of PRDM9 in C57BL/6 mice. This change repositions DSB hotspots and completely restores fertility in male hybrids. Here we show that alteration of one Prdm9 allele impacts the behaviour of DSBs controlled by the other allele at chromosome-wide scales. These effects correlate strongly with the degree to which each PRDM9 variant binds both homologues at the DSB sites it controls. Furthermore, higher genome-wide levels of such 'symmetric' PRDM9 binding associate with increasing fertility measures, and comparisons of individual hotspots suggest binding symmetry plays a downstream role in the recombination process. These findings reveal that subspecies-specific degradation of PRDM9 binding sites by meiotic drive, which steadily increases asymmetric PRDM9 binding, has impacts beyond simply changing hotspot positions, and strongly support a direct involvement in hybrid infertility. Because such meiotic drive occurs across mammals, PRDM9 may play a wider, yet transient, role in the early stages of speciation.

Original publication

DOI

10.1038/nature16931

Type

Journal article

Journal

Nature

Publication Date

11/02/2016

Volume

530

Pages

171 - 176

Keywords

Alleles, Animals, Binding Sites, Chromosome Pairing, Chromosomes, Mammalian, DNA Breaks, Double-Stranded, Female, Genetic Speciation, Histone-Lysine N-Methyltransferase, Humans, Hybridization, Genetic, Infertility, Male, Meiosis, Mice, Mice, Inbred C57BL, Protein Binding, Protein Engineering, Protein Structure, Tertiary, Recombination, Genetic, Zinc Fingers