Plasticity of Mitochondrial Translation

Trends Cell Biol. 2017 Oct;27(10):712-721. doi: 10.1016/j.tcb.2017.05.004. Epub 2017 Jun 9.

Abstract

Mitochondria maintained a genome during evolution to synthesize core subunits of the oxidative phosphorylation system. Expression of the mitochondrial genome requires intraorganellar replication, transcription, and translation. Membrane-associated ribosomes translate mitochondrial-encoded proteins and facilitate co-translational insertion of newly synthesized polypeptides into the inner membrane. Considering that mitochondrial-encoded proteins assemble with imported, nuclear-encoded proteins into enzyme complexes of the oxidative phosphorylation system, it is expected that expression of mitochondrial genes should adapt to the availability of their nuclear-encoded partners. Recent work shows that mitochondrial translation is influenced by the cellular environment. We discuss how mitochondrial translation is affected by the cellular environment and propose models of translational plasticity that modulate mitochondrial translation in response to the availability of imported proteins.

Keywords: OXPHOS assembly; mitochondria; mitochondrial ribosome; respiratory chain; translation regulation.

Publication types

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

MeSH terms

  • Animals
  • Humans
  • Mitochondria / metabolism*
  • Mitochondria / physiology*
  • Mitochondrial Proteins / metabolism*
  • Multienzyme Complexes / metabolism
  • Nuclear Proteins / metabolism
  • Oxidative Phosphorylation
  • Protein Biosynthesis / physiology*
  • Protein Transport / physiology
  • RNA, Messenger / metabolism
  • Ribosomes / metabolism
  • Ribosomes / physiology

Substances

  • Mitochondrial Proteins
  • Multienzyme Complexes
  • Nuclear Proteins
  • RNA, Messenger