GENOME STRUCTURE AND THE BENEFIT OF SEX
Article first published online: 5 NOV 2010
DOI: 10.1111/j.1558-5646.2010.01144.x
© 2010 The Author(s). Evolution© 2010 The Society for the Study of Evolution
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How to Cite
Watson, R. A., Weinreich, D. M. and Wakeley, J. (2011), GENOME STRUCTURE AND THE BENEFIT OF SEX. Evolution, 65: 523–536. doi: 10.1111/j.1558-5646.2010.01144.x
Publication History
- Issue published online: 27 JAN 2011
- Article first published online: 5 NOV 2010
- Accepted manuscript online: 1 OCT 2010 06:57AM EST
- Received January 5, 2010, Accepted July 27, 2010
- Abstract
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- References
- Cited By
Keywords:
- Epistasis;
- models/simulations;
- molecular evolution;
- population genetics;
- sex
We examine the behavior of sexual and asexual populations in modular multipeaked fitness landscapes and show that sexuals can systematically reach different, higher fitness adaptive peaks than asexuals. Whereas asexuals must move against selection to escape local optima, sexuals reach higher fitness peaks reliably because they create specific genetic variants that “skip over” fitness valleys, moving from peak to peak in the fitness landscape. This occurs because recombination can supply combinations of mutations in functional composites or “modules,” that may include individually deleterious mutations. Thus when a beneficial module is substituted for another less-fit module by sexual recombination it provides a genetic variant that would require either several specific simultaneous mutations in an asexual population or a sequence of individual mutations some of which would be selected against. This effect requires modular genomes, such that subsets of strongly epistatic mutations are tightly physically linked. We argue that such a structure is provided simply by virtue of the fact that genomes contain many genes each containing many strongly epistatic nucleotides. We briefly discuss the connections with “building blocks” in the evolutionary computation literature. We conclude that there are conditions in which sexuals can systematically evolve high-fitness genotypes that are essentially unevolvable for asexuals.

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