Journal Article

A bifunctional protein regulates mitochondrial protein synthesis

Tara R. Richman, Stefan M.K. Davies, Anne-Marie J. Shearwood, Judith A. Ermer, Louis H. Scott, Moira E. Hibbs, Oliver Rackham and Aleksandra Filipovska

in Nucleic Acids Research

Volume 42, issue 9, pages 5483-5494
Published in print May 2014 | ISSN: 0305-1048
Published online March 2014 | e-ISSN: 1362-4962 | DOI: http://dx.doi.org/10.1093/nar/gku179

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Mitochondrial gene expression is predominantly regulated at the post-transcriptional level and mitochondrial ribonucleic acid (RNA)-binding proteins play a key role in RNA metabolism and protein synthesis. The AU-binding homolog of enoyl-coenzyme A (CoA) hydratase (AUH) is a bifunctional protein with RNA-binding activity and a role in leucine catabolism. AUH has a mitochondrial targeting sequence, however, its role in mitochondrial function has not been investigated. Here, we found that AUH localizes to the inner mitochondrial membrane and matrix where it associates with mitochondrial ribosomes and regulates protein synthesis. Decrease or overexpression of the AUH protein in cells causes defects in mitochondrial translation that lead to changes in mitochondrial morphology, decreased mitochondrial RNA stability, biogenesis and respiratory function. Because of its role in leucine metabolism, we investigated the importance of the catalytic activity of AUH and found that it affects the regulation of mitochondrial translation and biogenesis in response to leucine.

Journal Article.  6457 words.  Illustrated.

Subjects: Chemistry ; Biochemistry ; Bioinformatics and Computational Biology ; Genetics and Genomics ; Molecular and Cell Biology

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