Gene duplication and gene conversion shape the evolution of archaeal chaperonins

John M. Archibald, Andrew J. Roger

Research output: Contribution to journalArticlepeer-review

47 Citations (Scopus)

Abstract

Chaperonins are multi-subunit double-ring complexes that mediate the folding of nascent or denatured proteins. Gene duplication has been a potent force in the evolution of chaperonins in Archaea. Here we show that gene conversion has also been an important factor. We utilized a novel maximum likehood-based phylogenetic method for scanning DNA sequence alignments for regions of anomalous phylogenetic signal, such as those affected by gene conversion. Our results suggest that in crenarchaeotes, where an ancient gene duplication producing α and β subunits took place in the common ancestor of the Pyrodictium, Aeropyrum, Pyrobaculum and Sulfolobus lineages, multiple independent gene conversions have occurred between the α and β genes independently in each of these groups. Significantly, the conversions have repeatedly homogenized the region of the gene encoding the substrate-binding domain. This suggests that while the α and β subunits in crenarchaeotes share only 50-60% overall amino acid sequence identity, they do not possess distinct roles in the binding of substrate. Cryptic gene conversion between distantly related paralogs may be more common than is currently appreciated, and could be a significant factor in slowing the functional differentiation of proteins encoded by duplicate genes long after their duplication.

Original languageEnglish
Pages (from-to)1041-1050
Number of pages10
JournalJournal of Molecular Biology
Volume316
Issue number5
DOIs
Publication statusPublished - 2002

Bibliographical note

Funding Information:
We thank J. Andersson and A. Simpson for critical review of the manuscript, C. Blouin for help with molecular modeling and the Roger and Doolittle labs for helpful discussion. This work was supported by an NSERC grant (227085-00) awarded to A.J.R. J.M.A. was supported by a CIHR Doctoral Research Award and, subsequently, NSERC grant 227085-00 awarded to A.J.R.

ASJC Scopus Subject Areas

  • Biophysics
  • Structural Biology
  • Molecular Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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