MTG1 Codes for a Conserved Protein Required for Mitochondrial Translation

Author:

Barrientos Antoni1,Korr Daniel1,Barwell Karen J.1,Sjulsen Christian1,Gajewski Carl D.2,Manfredi Giovanni2,Ackerman Sharon3,Tzagoloff Alexander1

Affiliation:

1. Department of Biological Sciences, Columbia University, New York, New York 10027

2. Department of Neurology and Neuroscience, Cornell University, New York, New York 10021

3. Department of Surgery, Wayne State University School of Medicine, Detroit, Michigan 48201

Abstract

The MTG1 gene of Saccharomyces cerevisiae, corresponding to ORF YMR097c on chromosome XIII, codes for a mitochondrial protein essential for respiratory competence. A human homologue of Mtg1p capable of partially rescuing the respiratory deficiency of a yeast mtg1 mutant has also been localized in mitochondria. Mtg1p is a member of a family of GTPases with largely unknown functions. The respiratory deficiency of mtg1 mutants stems from a defect in mitochondrial protein synthesis. Mutations in the 21S rRNA locus are able to suppress the translation defect of mtg1 null mutants. This points to the 21S rRNA or the large ribosomal subunit as the most likely target of Mtg1p action. The presence of mature size 15S and 21S mitochondrial rRNAs in mtg1 mutants excludes Mtg1p from being involved in transcription or processing of these RNAs. More likely, Mtg1p functions in assembly of the large ribosomal subunit. This is consistent with the peripheral localization of Mtg1p on the matrix side of the inner membrane and the results of in vivo mitochondrial translation assays in a temperature-sensitive mtg1 mutant.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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