The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease

EMBO J. 1998 Aug 17;17(16):4837-47. doi: 10.1093/emboj/17.16.4837.

Abstract

Yta10p (Afg3p) and Yta12p (Rcal1p), members of the conserved AAA family of ATPases, are subunits of the mitochondrial m-AAA protease, an inner membrane ATP-dependent metallopeptidase. Deletion of YTA10 or YTA12 impairs degradation of non-assembled inner membrane proteins and assembly of respiratory chain complexes. Mutations of the proteolytic sites in either YTA10 or YTA12 have been shown to inhibit proteolysis of membrane-integrated polypeptides but not the respiratory competence of the cells, suggesting additional activities of Yta10p and Yta12p. Here we demonstrate essential proteolytic functions of the m-AAA protease in the biogenesis of the respiratory chain. Cells harbouring proteolytically inactive forms of both Yta10p and Yta12p are respiratory deficient and exhibit a pleiotropic phenotype similar to Deltayta10 and Deltayta12 cells. They show deficiencies in expression of the intron-containing mitochondrial genes COX1 and COB. Splicing of COX1 and COB transcripts is impaired in mitochondria lacking m-AAA protease, whilst transcription and translation can proceed in the absence of Yta10p or Yta12p. The function of the m-AAA protease appears to be confined to introns encoding mRNA maturases. Our results reveal an overlapping substrate specificity of the subunits of the m-AAA protease and explain the impaired assembly of respiratory chain complexes by defects in expression of intron-containing genes in mitochondria lacking m-AAA protease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism
  • Cyclooxygenase 1
  • Electron Transport
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Hydrolysis
  • Introns
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Metalloendopeptidases / genetics
  • Mitochondria / enzymology
  • Mitochondria / metabolism*
  • Mutation
  • Phenotype
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Protease Inhibitors
  • Protein Processing, Post-Translational
  • RNA Splicing
  • Saccharomyces cerevisiae Proteins*
  • Substrate Specificity

Substances

  • Fungal Proteins
  • Isoenzymes
  • Protease Inhibitors
  • Saccharomyces cerevisiae Proteins
  • Cyclooxygenase 1
  • Prostaglandin-Endoperoxide Synthases
  • Electron Transport Complex IV
  • Metalloendopeptidases
  • m-AAA proteases
  • Adenosine Triphosphatases
  • AFG3 protein, S cerevisiae