Co-evolution of mitochondrial tRNA import and codon usage determines translational efficiency in the green alga Chlamydomonas

PLoS Genet. 2012 Sep;8(9):e1002946. doi: 10.1371/journal.pgen.1002946. Epub 2012 Sep 20.

Abstract

Mitochondria from diverse phyla, including protozoa, fungi, higher plants, and humans, import tRNAs from the cytosol in order to ensure proper mitochondrial translation. Despite the broad occurrence of this process, our understanding of tRNA import mechanisms is fragmentary, and crucial questions about their regulation remain unanswered. In the unicellular green alga Chlamydomonas, a precise correlation was found between the mitochondrial codon usage and the nature and amount of imported tRNAs. This led to the hypothesis that tRNA import might be a dynamic process able to adapt to the mitochondrial genome content. By manipulating the Chlamydomonas mitochondrial genome, we introduced point mutations in order to modify its codon usage. We find that the codon usage modification results in reduced levels of mitochondrial translation as well as in subsequent decreased levels and activities of respiratory complexes. These effects are linked to the consequential limitations of the pool of tRNAs in mitochondria. This indicates that tRNA mitochondrial import cannot be rapidly regulated in response to a novel genetic context and thus does not appear to be a dynamic process. It rather suggests that the steady-state levels of imported tRNAs in mitochondria result from a co-evolutive adaptation between the tRNA import mechanism and the requirements of the mitochondrial translation machinery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Cell Respiration / genetics
  • Chlamydomonas / genetics*
  • Codon / genetics
  • Evolution, Molecular
  • Genome, Mitochondrial
  • Membrane Potential, Mitochondrial
  • Mitochondria / genetics*
  • Mitochondria / metabolism
  • Point Mutation
  • Protein Biosynthesis*
  • RNA, Transfer / genetics*
  • RNA, Transfer / metabolism

Substances

  • Codon
  • RNA, Transfer

Grants and funding

CR was supported by Fonds National de la Recherche Scientifique (FNRS) (grants 1.5.255.08, 2.4.601.08, and 2.4567.11), European FP7-funded Sunbiopath project (GA 245070), and “Fonds Spéciaux du Conseil de la Recherche” from the University of Liège. TS was supported by the European FP7-funded IEF (FP7/2007-2013) (GA 220808) and the Agence Nationale pour la Recherche (ANR) (grant ANR-09-BLAN-0240-01). VL was supported by Formation à la Recherche dans l'Industrie et l'Agriculture (FRIA fellowship) and European FP7-funded Sunbiopath project (GA245050). NB was supported by the ANR (grant JCJC06-0163). PM was supported by FNRS (grants 2.4581.10 and 2.4531.09) and the “Fonds Spéciaux du Conseil de la Recherche” from the University of Liège. LM-D was supported by Centre National de la Recherche Scientifique (CNRS) and by the French National Program “Investissement d'Avenir” (Labex MitoCross) from the University of Strasbourg. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.