Large-scale analyses of synonymous substitution rates can be sensitive to assumptions about the process of mutation

Stéphane Aris-Brosou, Joseph P. Bielawski

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

A popular approach to examine the roles of mutation and selection in the evolution of genomes has been to consider the relationship between codon bias and synonymous rates of molecular evolution. A significant relationship between these two quantities is taken to indicate the action of weak selection on substitutions among synonymous codons. The neutral theory predicts that the rate of evolution is inversely related to the level of functional constraint. Therefore, selection against the use of non-preferred codons among those coding for the same amino acid should result in lower rates of synonymous substitution as compared with sites not subject to such selection pressures. However, reliably measuring the extent of such a relationship is problematic, as estimates of synonymous rates are sensitive to our assumptions about the process of molecular evolution. Previous studies showed the importance of accounting for unequal codon frequencies, in particular when synonymous codon usage is highly biased. Yet, unequal codon frequencies can be modeled in different ways, making different assumptions about the mutation process. Here we conduct a simulation study to evaluate two different ways of modeling uneven codon frequencies and show that both model parameterizations can have a dramatic impact on rate estimates and affect biological conclusions about genome evolution. We reanalyze three large data sets to demonstrate the relevance of our results to empirical data analysis.

Original languageEnglish
Pages (from-to)58-64
Number of pages7
JournalGene
Volume378
Issue number1-2
DOIs
Publication statusPublished - Aug 15 2006

Bibliographical note

Funding Information:
This work was funded by an NSERC grant (DG 311625) to SAB. JPB was partially supported by a start-up grant from the Genome Atlantic Centre of Genome Canada, and by an NSERC grant (DG 298394). We thank Dr Giorgio Bernardi and an anonymous referee for comments that helped improve the manuscript.

ASJC Scopus Subject Areas

  • Genetics

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