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.

Highlights

  • Mitochondria are organelles found in almost all eukaryotic cells [1]

  • In some organisms where mitochondrial genomes are apparently equipped with a minimal set of transfer RNAs (tRNAs) genes sufficient for mitochondrial translation [3], tRNA import can occur under certain circumstances, as documented in yeast and in human [4,5]

  • They contain their own genome that encodes a few but essential proteins. Their synthesis requires functional mitochondrial translational machinery that necessitates a full set of transfer RNAs

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Summary

Introduction

Mitochondria are organelles found in almost all eukaryotic cells [1] They contain a genetic system that encodes a number of protein-coding genes involved in oxidative phosphorylation, which yields the bulk of the ATP made in cells. The synthesis of these mitochondria-encoded proteins is essential for life and requires a complete set of transfer RNAs (tRNAs). The number of mitochondrial tRNA genes is not sufficient to ensure mitochondrial translation and nucleus-encoded tRNAs have to be imported from the cytosol to mitochondria. In some organisms where mitochondrial genomes are apparently equipped with a minimal set of tRNA genes sufficient for mitochondrial translation [3], tRNA import can occur under certain circumstances, as documented in yeast and in human [4,5]

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