A genomic region containing RNF212 is associated with sexually-dimorphic recombination rate variation in wild Soay sheep (Ovis aries).

A genomic region containing RNF212 is associated with sexually-dimorphic recombination rate variation in wild Soay sheep (Ovis aries).

Susan E Johnston, Jon Slate, Josephine M Pemberton
doi: http://dx.doi.org/10.1101/024869

Meiotic recombination breaks down linkage disequilibrium and forms new haplotypes, meaning that it is an important driver of diversity in eukaryotic genomes. Understanding the causes of variation in recombination rate is not only important in interpreting and predicting evolutionary phenomena, but also for understanding the potential of a population to respond to selection. Yet, there remains little data on if, how and why recombination rate varies in natural populations. Here, we used extensive pedigree and high-density SNP information in a wild population of Soay sheep (Ovis aries) to determine individual crossovers in 3330 gametes from 813 individuals. Using these data, we investigated the recombination landscape and the genetic architecture of individual autosomal recombination rate. The population was strongly heterochiasmic (male to female linkage map ratio = 1.31), driven by significantly elevated levels of male recombination in sub-telomeric regions. Autosomal recombination rate was heritable in both sexes (h2 = 0.16 & 0.12 in females and males, respectively), but with different genetic architectures. In females, 46.7% of heritable variation was explained by a sub-telomeric region on chromosome 6; a genome-wide association study showed the strongest associations at RNF212, with further associations observed at a nearby ~374kb region of complete linkage disequilibrium containing three additional candidate loci, CPLX1, GAK and PCGF3. This region did not affect male recombination rate. A second region on chromosome 7 containing REC8 and RNF212B explained 26.2% of heritable variation in recombination rate in both sexes, with further single locus associations identified on chromosome 3. Our findings provide a key empirical example of the genetic architecture of recombination rate in a wild mammal population with male-biased crossover frequency.


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