Abstract

Two-locus two-allele models are among the most studied models in population genetics. The reason is that they are the simplest models to explore the role of epistasis for a variety of important evolutionary problems, including the maintenance of polymorphism and the evolution of genetic incompatibilities. Many specific types of models have been explored. However, due to the mathematical complexity arising from the fact that epistasis generates linkage disequilibrium, few general insights have emerged. Here, we study a simpler problem by assuming that linkage disequilibrium can be ignored. This is a valid approximation if selection is sufficiently weak relative to recombination. The goal of our paper is to characterize all possible equilibrium structures, or more precisely and general, all robust phase portraits or evolutionary flows arising from this weak-selection dynamics. For general fitness matrices, we have not fully accomplished this goal, because some cases remain undecided. However, for many specific classes of fitness schemes, including additive fitnesses, purely additive-by-additive epistasis, haploid selection, multilinear epistasis, marginal overdominance or underdominance, and the symmetric viability model, we obtain complete characterizations of the possible equilibrium structures and, in several cases, even of all possible phase portraits. A central point in our analysis is the inference of the number and stability of fully polymorphic equilibria from the boundary flow, i.e., from the dynamics at the four marginal single-locus subsystems. The key mathematical ingredient for this is index theory. The specific form of epistasis has both a big influence on the possible boundary flows as well as on the internal equilibrium structure admitted by a given boundary flow.

Highlights

  • One of the central goals of the pioneers of population genetics was to demonstrate that the inheritance and evolution of continuously varying traits could be explained on the basis of Mendelian genetics (Fisher 1918, 1930)

  • Mean fitness is a Lyapunov function (Ewens 1969), all equilibria are in linkage equilibrium, and, generically, every trajectory converges to an equilibrium point (Karlin and Liberman 1978, 1990; Nagylaki et al 1999)

  • The analysis of this simplified model has immediate implications for the full twolocus two-allele model. This is a consequence of a general theorem by Nagylaki et al (1999), which applies to multilocus systems. These authors proved under weak technical assumptions that if selection is much weaker than recombination, after an evolutionarily short period, in which linkage disequilibrium decays to close to zero, the dynamics of the full model is governed by this weak-selection limit

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Summary

Introduction

One of the central goals of the pioneers of population genetics was to demonstrate that the inheritance and evolution of continuously varying traits could be explained on the basis of Mendelian genetics (Fisher 1918, 1930). The existence of stable limit cycles has been demonstrated both for the continuous-time model (Akin 1979, 1982) and the discrete-time model (Hastings 1981b; Hofbauer and Iooss 1984) Such complex behavior cannot occur if loci are assumed to be independent, i.e., if linkage equilibrium is imposed. This is a consequence of a general theorem by Nagylaki et al (1999), which applies to multilocus systems These authors proved under weak technical assumptions that if selection is much weaker than recombination, after an evolutionarily short period, in which linkage disequilibrium decays to close to zero, the dynamics of the full model (either in discrete or in continuous time) is governed by this weak-selection limit. Under the above symmetry assumptions, the fitnesses of genotypes are completely specified by the following matrix: A1 A1 A1 A2 A2 A2

B2 w22 w24 w44
Equilibria and their stability
Equilibrium structure and flows
Flows on the boundary
Extended boundary flows
Established equilibrium structures and phase portraits
Permanence
Continuous isoclines: marginal overdominance or underdominance
Linear isoclines
The additive fitness model
The haploid model
The multilinear epistasis model
Equal locus effects
The symmetric viability model
10 Discussion
10.2 Permanence
10.3 Marginal overdominance or underdominance
10.5 Multilinear epistasis
10.6 Equivalent loci
10.7 The symmetric viability model
10.8 Multiplicative fitnesses
10.9 Inferring stable two-locus polymorphisms
The external eigenvalues
Proofs for the symmetric viability model
Full Text
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