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Letter

Nature 443, 89-92 (7 September 2006) | doi:10.1038/nature05049; Received 19 May 2006; Accepted 5 July 2006

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Interference among deleterious mutations favours sex and recombination in finite populations

Peter D. Keightley1 & Sarah P. Otto2

  1. Institute of Evolutionary Biology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, UK
  2. Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, British Columbia V6T 1Z4, Canada

Correspondence to: Peter D. Keightley1 Correspondence and requests for materials should be addressed to P.K. (Email: keightley.nature2006@spambob.net).

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Sex and recombination are widespread, but explaining these phenomena has been one of the most difficult problems in evolutionary biology. Recombination is advantageous when different individuals in a population carry different advantageous alleles1, 2. By bringing together advantageous alleles onto the same chromosome, recombination speeds up the process of adaptation1, 3, 4, 5 and opposes the fixation of harmful mutations by means of Muller's ratchet4, 5. Nevertheless, adaptive substitutions favour sex and recombination only if the rate of adaptive mutation is high1, 6, and Muller's ratchet operates only in small or asexual populations7. Here, by tracking the fate of modifier alleles that alter the frequency of sex and recombination, we show that background selection against deleterious mutant alleles provides a stochastic advantage to sex and recombination that increases with population size. The advantage arises because, with low levels of recombination, selection at other loci severely reduces the effective population size and genetic variance in fitness at a focal locus8 (the Hill–Robertson effect), making a population less able to respond to selection and to rid itself of deleterious mutations. Sex and recombination reveal the hidden genetic variance in fitness by combining chromosomes of intermediate fitness to create chromosomes that are relatively free of (or are loaded with) deleterious mutations. This increase in genetic variance within finite populations improves the response to selection and generates a substantial advantage to sex and recombination that is fairly insensitive to the form of epistatic interactions between deleterious alleles. The mechanism supported by our results offers a robust and broadly applicable explanation for the evolutionary advantage of recombination and can explain the spread of costly sex.

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