Compensating the Fitness Costs of Synonymous Mutations

Mol Biol Evol. 2016 Jun;33(6):1461-77. doi: 10.1093/molbev/msw028. Epub 2016 Feb 16.

Abstract

Synonymous mutations do not change the sequence of the polypeptide but they may still influence fitness. We investigated in Salmonella enterica how four synonymous mutations in the rpsT gene (encoding ribosomal protein S20) reduce fitness (i.e., growth rate) and the mechanisms by which this cost can be genetically compensated. The reduced growth rates of the synonymous mutants were correlated with reduced levels of the rpsT transcript and S20 protein. In an adaptive evolution experiment, these fitness impairments could be compensated by mutations that either caused up-regulation of S20 through increased gene dosage (due to duplications), increased transcription of the rpsT gene (due to an rpoD mutation or mutations in rpsT), or increased translation from the rpsT transcript (due to rpsT mutations). We suggest that the reduced levels of S20 in the synonymous mutants result in production of a defective subpopulation of 30S subunits lacking S20 that reduce protein synthesis and bacterial growth and that the compensatory mutations restore S20 levels and the number of functional ribosomes. Our results demonstrate how specific synonymous mutations can cause substantial fitness reductions and that many different types of intra- and extragenic compensatory mutations can efficiently restore fitness. Furthermore, this study highlights that also synonymous sites can be under strong selection, which may have implications for the use of dN/dS ratios as signature for selection.

Keywords: Salmonella typhimurium; bacterial fitness; compensatory mutations; experimental evolution; protein synthesis.; synonymous mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Evolution, Molecular
  • Genetic Fitness*
  • Protein Biosynthesis / genetics
  • RNA, Messenger / genetics
  • Ribosomal Proteins / genetics*
  • Ribosomal Proteins / metabolism
  • Salmonella enterica / genetics*
  • Salmonella enterica / metabolism
  • Salmonella typhimurium / genetics
  • Silent Mutation*

Substances

  • RNA, Messenger
  • Ribosomal Proteins
  • ribosomal protein S20