Abstract

BackgroundUnderstanding interactions between mutations and how they affect fitness is a central problem in evolutionary biology that bears on such fundamental issues as the structure of fitness landscapes and the evolution of sex. To date, analyses of fitness landscapes have focused either on the overall directional curvature of the fitness landscape or on the distribution of pairwise interactions. In this paper, we propose and employ a new mathematical approach that allows a more complete description of multi-way interactions and provides new insights into the structure of fitness landscapes.ResultsWe apply the mathematical theory of gene interactions developed by Beerenwinkel et al. to a fitness landscape for Escherichia coli obtained by Elena and Lenski. The genotypes were constructed by introducing nine mutations into a wild-type strain and constructing a restricted set of 27 double mutants. Despite the absence of mutants higher than second order, our analysis of this genotypic space points to previously unappreciated gene interactions, in addition to the standard pairwise epistasis. Our analysis confirms Elena and Lenski's inference that the fitness landscape is complex, so that an overall measure of curvature obscures a diversity of interaction types. We also demonstrate that some mutations contribute disproportionately to this complexity. In particular, some mutations are systematically better than others at mixing with other mutations. We also find a strong correlation between epistasis and the average fitness loss caused by deleterious mutations. In particular, the epistatic deviations from multiplicative expectations tend toward more positive values in the context of more deleterious mutations, emphasizing that pairwise epistasis is a local property of the fitness landscape. Finally, we determine the geometry of the fitness landscape, which reflects many of these biologically interesting features.ConclusionA full description of complex fitness landscapes requires more information than the average curvature or the distribution of independent pairwise interactions. We have proposed a mathematical approach that, in principle, allows a complete description and, in practice, can suggest new insights into the structure of real fitness landscapes. Our analysis emphasizes the value of non-independent genotypes for these inferences.

Highlights

  • Understanding interactions between mutations and how they affect fitness is a central problem in evolutionary biology that bears on such fundamental issues as the structure of fitness landscapes and the evolution of sex

  • Several studies have sought to examine the form and prevalence of epistatic interactions by measuring the fitness effects of numerous mutations alone and in combination in viruses, bacteria, fungi, and animals [2,27,28,29,30,31]. These analyses have focused on the overall directional curvature of fitness as a function of the number of mutations, on the distribution of pairwise interactions, or on both

  • The goal of our analysis is to describe the geometry of the E. coli fitness landscape obtained by Elena and Lenski [2]

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Summary

Introduction

Understanding interactions between mutations and how they affect fitness is a central problem in evolutionary biology that bears on such fundamental issues as the structure of fitness landscapes and the evolution of sex. The surface of a landscape may represent the relative fitness of individual types, or the average fitness of a population. In the former case, the underlying coordinates describe either the genotypic or phenotypic state of an individual; in the latter case, the coordinates describe either gene frequencies or average phenotypes in a population. Our paper concerns the mathematical analysis and interpretation of fitness landscapes where the height of the surface represents the relative fitness of individuals and the coordinates are different genotypes. In this evolutionary context, fitness measures the expected reproductive success of an individual having a specific genotype in some particular environment. A fitness landscape is given by assigning to each genotype g its fitness wg

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