Reconstructing the evolutionary history of the centriole from protein components

J Cell Sci. 2010 May 1;123(Pt 9):1407-13. doi: 10.1242/jcs.064873. Epub 2010 Apr 13.

Abstract

Centrioles are highly conserved structures that fulfil important cellular functions, such as nucleation of cilia and flagella (basal-body function) and organisation of pericentriolar material to form the centrosome. The evolution of these functions can be inferred from the distribution of the molecular components of extant centrioles and centrosomes. Here, we undertake an evolutionary analysis of 53 proteins known either for centriolar association or for involvement in cilia-associated pathologies. By linking protein distribution in 45 diverse eukaryotes with organism biology, we provide molecular evidence to show that basal-body function is ancestral, whereas the presence of the centrosome is specific to the Holozoa. We define an ancestral centriolar inventory of 14 core proteins, Polo-like-kinase, and proteins associated with Bardet-Biedl syndrome (BBS) and Meckel-Gruber syndrome. We show that the BBSome is absent from organisms that produce cilia only for motility, predicting a dominant and ancient role for this complex in sensory function. We also show that the unusual centriole of Caenorhabditis elegans is highly divergent in both protein composition and sequence. Finally, we demonstrate a correlation between the presence of specific centriolar proteins and eye evolution. This correlation is used to predict proteins with functions in the development of ciliary, but not rhabdomeric, eyes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Caenorhabditis elegans / metabolism
  • Centrioles / chemistry*
  • Centrioles / enzymology
  • Centrioles / genetics
  • Centrioles / metabolism*
  • Cilia / metabolism
  • Eukaryotic Cells / metabolism
  • Evolution, Molecular*
  • Humans
  • Phosphotransferases / metabolism
  • Phylogeny
  • Proteins / metabolism*
  • Tubulin / genetics

Substances

  • Proteins
  • Tubulin
  • Phosphotransferases