Originally published as Genetics Published Articles Ahead of Print on March 17, 2006.

Genetics, Vol. 173, 589-597, June 2006, Copyright © 2006
doi:10.1534/genetics.105.053108

Effect of Varying Epistasis on the Evolution of Recombination

Roger D. Kouyos*, Sarah P. Otto{dagger} and Sebastian Bonhoeffer*,1

* Integrative Biology, ETH Zürich, ETH Zentrum CHN, CH-8092 Zürich, Switzerland and {dagger} Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada

1 Corresponding author: Theoretical Biology, ETH Zürich, ETH Zentrum CHN, Universitaetsstr. 16, CH-8092 Zürich, Switzerland.
E-mail: seb{at}env.ethz.ch

Whether recombination decelerates or accelerates a population's response to selection depends, at least in part, on how fitness-determining loci interact. Realistically, all genomes likely contain fitness interactions both with positive and with negative epistasis. Therefore, it is crucial to determine the conditions under which the potential beneficial effects of recombination with negative epistasis prevail over the detrimental effects of recombination with positive epistasis. Here, we examine the simultaneous effects of diverse epistatic interactions with different strengths and signs in a simplified model system with independent pairs of interacting loci and selection acting only on the haploid phase. We find that the average form of epistasis does not predict the average amount of linkage disequilibrium generated or the impact on a recombination modifier when compared to results using the entire distribution of epistatic effects and associated single-mutant effects. Moreover, we show that epistatic interactions of a given strength can produce very different effects, having the greatest impact when selection is weak. In summary, we observe that the evolution of recombination at mutation–selection balance might be driven by a small number of interactions with weak selection rather than by the average epistasis of all interactions. We illustrate this effect with an analysis of published data of Saccharomyces cerevisiae. Thus to draw conclusions on the evolution of recombination from experimental data, it is necessary to consider the distribution of epistatic interactions together with the associated selection coefficients.




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