Shifting Balance on a Static Mutation-Selection Landscape: A Novel Scenario of Positive Selection

Mol Biol Evol. 2017 Feb 1;34(2):391-407. doi: 10.1093/molbev/msw237.

Abstract

A version of the mechanistic mutation-selection (MutSel) model that accounts for temporal dynamics at a site is presented. This is used to show that the rate ratio dN/dS at a site can be transiently >1 even when fitness coefficients are fixed or the fitness landscape is static. This occurs whenever a site drifts away from its fitness peak and is then forced back by selection, a process reminiscent of shifting balance. Shifting balance is strongest when the substitution process is not dominated by selection or drift, but admits interplay between the two. Under this condition, site-specific changes in dN/dS were inferred in 78-100% of trials, and positive selection (i.e., dN/dS>1) in 10-40% of trials, when sequence alignments generated under MutSel were fitted to two popular phenomenological branch-site models. These results demonstrate that positive selection can occur without a change in fitness regime, and that this is detectable by branch-site models. In addition, MutSel is used to show that a site can be occupied by a sub-optimal amino acid for long periods on a fixed landscape when selection is stringent. This has implications for the interpretation of constant-but-different site patterns typically attributed to changes in fitness. Furthermore, a version of MutSel with episodic changes in fitness coefficients is used to illustrate systematic differences between parameters used to generate data under MutSel and their counterparts estimated by a simple codon model. Motivated by a discrepancy in the literature, interpretation of dN/dS in the context of MutSel is also discussed.

Keywords: codon models; dN/dS; population genetics; positive selection; site-specific fitness landscapes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Amino Acids / genetics
  • Animals
  • Codon*
  • Drosophila
  • Evolution, Molecular
  • Genetic Variation
  • Genetics, Population / methods*
  • Humans
  • Models, Genetic*
  • Mutation
  • Phylogeny
  • Selection, Genetic*
  • Sequence Alignment

Substances

  • Amino Acids
  • Codon