A small Tim homohexamer in the relict mitochondrion of Cryptosporidium

Mol Biol Evol. 2012 Jan;29(1):113-22. doi: 10.1093/molbev/msr165. Epub 2011 Oct 6.

Abstract

The apicomplexan parasite Cryptosporidium parvum possesses a mitosome, a relict mitochondrion with a greatly reduced metabolic capability. This mitosome houses a mitochondrial-type protein import apparatus, but elements of the protein import pathway have been reduced, and even lost, through evolution. The small Tim protein family is a case in point. The genomes of C. parvum and related species of Cryptosporidium each encode just one small Tim protein, CpTimS. This observation challenged the tenet that small Tim proteins are always found in pairs as α3β3 hexamers. We show that the atypical CpTimS exists as a relatively unstable homohexamer, shedding light both on the early evolution of the small Tim protein family and on small Tim hexamer formation in contemporary eukaryotes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Carrier Proteins / chemistry*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cryptosporidium / chemistry
  • Cryptosporidium / genetics*
  • Evolution, Molecular
  • Mitochondria / chemistry
  • Mitochondria / genetics*
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Molecular Sequence Data
  • Protein Conformation
  • Protein Multimerization
  • Protein Subunits
  • Sequence Alignment

Substances

  • Carrier Proteins
  • Molecular Chaperones
  • Protein Subunits