Abstract
Despite being linked to the fundamental processes of chromosome segregation and offspring diversification, meiotic recombination rates vary within and between species. Recent years have seen progress in quantifying recombination rate evolution across multiple temporal and genomic scales. Nevertheless, the level of variation in recombination rate within wild populations—a key determinant of evolution in this trait—remains poorly documented on the genomic scale. To address this notable gap, we used immunofluorescent cytology to quantify genome-wide recombination rates in males from a wild population of the white-footed mouse, Peromyscus leucopus. For comparison, we measured recombination rates in a second population of male P. leucopus raised in the laboratory and in male deer mice from the subspecies Peromyscus maniculatus bairdii. Although we found differences between individuals in the genome-wide recombination rate, levels of variation were low—within populations, between populations, and between species. Quantification of synaptonemal complex length and crossover positions along chromosome 1 using a novel automated approach also revealed conservation in broad-scale crossover patterning, including strong crossover interference. We propose stabilizing selection targeting recombination or correlated processes as the explanation for these patterns.
Highlights
Meiotic recombination is one of the main sources of genetic variation
Little variation in recombination rate among wild P. leucopus bivalents could have been achiasmate, some might have harbored crossovers generated by the MLH1-independent pathway, which is estimated to produce up to 10% of crossovers in house mice (Holloway et al 2008)
The genome-wide recombination rate was manually quantified by counting MLH1 foci along bivalents in each of 221 spermatocytes from a total of nine wild male P. leucopus (Table 1, Fig. 1)
Summary
Meiotic recombination is one of the main sources of genetic variation. Recombination can facilitate or hinder adaptation by disrupting deleterious or beneficial combinations of alleles at different loci and by changing additive genetic variance (Hill and Robertson 1966; Barton 1995; Charlesworth and Barton 1996; Stapley et al 2017). In virtually all species that reproduce through sex, recombination is critical to the proper segregation of homologous chromosomes during meiosis (Hassold and Hunt 2001). Despite the evolutionary and genetic significance of crossing over, the rate
Published Version
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