Recurrent paralogy in the evolution of archaeal chaperonins

John M. Archibald, John M. Logsdon, W. Ford Doolittle

Research output: Contribution to journalArticlepeer-review

87 Citations (Scopus)

Abstract

Chaperonins are multisubunit double-ring complexes that mediate the folding of nascent proteins [1,2]. In bacteria, chaperonins are homo-oligomeric and are composed of seven-membered rings. Eukaryotic and most archaeal chaperonin rings are eight-membered and exhibit varying degrees of hetero-oligomerism [3,4]. We have cloned and sequenced seven new genes encoding chaperonin subunits from the crenarchaeotes Sulfolobus solfataricus, S. acidocaldarius, S. shibatae and Desulfurococcus mobilis. Although some archaeal genomes possess a single chaperonin gene, most have two. We describe a third chaperonin-encoding gene (TF55-γ) from two Sulfolobus species; phylogenetic analyses indicate that the gene duplication producing TF55-γ-occurred within crenarchaeal evolution. The presence of TF55-γ in Sulfolobus correlates with their unique nine-membered chaperonin rings. Duplicate genes (paralogs) for chaperonins within archaeal genomes very often resemble each other more than they resemble chaperonin genes from other archaea. Our phylogenetic analyses suggest multiple independent gene duplications - at least seven among the archaea examined. The persistence of paralogous genes for chaperonin subunits in multiple archaeal lineages may involve a process of co-evolution, where chaperonin subunit heterogeneity changes independently of selection on function.

Original languageEnglish
Pages (from-to)1053-1056
Number of pages4
JournalCurrent Biology
Volume9
Issue number18
DOIs
Publication statusPublished - Aug 23 1999

Bibliographical note

Funding Information:
We thank members of the Sulfolobus solfataricus p2 genome sequencing project, D. Faguy, H.-P. Klenk and M. Schenk for Sulfolobus and Desulfurococcus genomic DNAs, A. Stoltzfus for mol2con.pl, O. Feeley for aa-dna-align.pl and Doolittle laboratory members for helpful discussion and critical review. This work was supported by a grant awarded to W.F.D. by the Medical Research Council (MRC) of Canada. J.M.A. is supported by an MRC studentship awarded to W.F.D. and by an MRC Doctoral Research Award. J.M.L. is supported by post doctoral fellowships from the MRC and NIH.

ASJC Scopus Subject Areas

  • General Biochemistry,Genetics and Molecular Biology
  • General Agricultural and Biological Sciences

PubMed: MeSH publication types

  • Comparative Study
  • Journal Article
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

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