The ribosome receptors Mrx15 and Mba1 jointly organize cotranslational insertion and protein biogenesis in mitochondria

Mol Biol Cell. 2018 Oct 1;29(20):2386-2396. doi: 10.1091/mbc.E18-04-0227. Epub 2018 Aug 9.

Abstract

Mitochondrial gene expression in Saccharomyces cerevisiae is responsible for the production of highly hydrophobic subunits of the oxidative phosphorylation system. Membrane insertion occurs cotranslationally on membrane-bound mitochondrial ribosomes. Here, by employing a systematic mass spectrometry-based approach, we discovered the previously uncharacterized membrane protein Mrx15 that interacts via a soluble C-terminal domain with the large ribosomal subunit. Mrx15 contacts mitochondrial translation products during their synthesis and plays, together with the ribosome receptor Mba1, an overlapping role in cotranslational protein insertion. Taken together, our data reveal how these ribosome receptors organize membrane protein biogenesis in mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electron Transport Complex IV / metabolism
  • Epistasis, Genetic
  • Gene Deletion
  • Mass Spectrometry
  • Membrane Proteins / metabolism*
  • Mitochondria / metabolism*
  • Mitochondrial Membranes / metabolism
  • Mitochondrial Proteins / metabolism*
  • Peptides / metabolism
  • Protein Binding
  • Protein Biosynthesis*
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Ribosome Subunits / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • MBA1 protein, S cerevisiae
  • Membrane Proteins
  • Mitochondrial Proteins
  • Peptides
  • Receptors, Cytoplasmic and Nuclear
  • Saccharomyces cerevisiae Proteins
  • ribosome receptor
  • Electron Transport Complex IV