Journal
CELL METABOLISM
Volume 30, Issue 1, Pages 190-+Publisher
CELL PRESS
DOI: 10.1016/j.cmet.2019.04.013
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Funding
- JPB Foundation
- National Institutes of Health [NIH DK061562, 1F32DK112638-01A1]
- Damon Runyon Cancer Research Foundation [R01-DK095072, R35-HL139424]
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Mitochondrial abundance and function are tightly controlled during metabolic adaptation but dysregulated in pathological states such as diabetes, neurodegeneration, cancer, and kidney disease. We show here that translation of PGC1 alpha, a key governor of mitochondrial biogenesis and oxidative metabolism, is negatively regulated by an upstream open reading frame (uORF) in the 5' untranslated region of its gene (PPARGC1A). We find that uORF-mediated translational repression is a feature of PPARGC1A orthologs from human to fly. Strikingly, whereas multiple inhibitory uORFs are broadly present in fish PPARGC1A orthologs, they are completely absent in the Atlantic bluefin tuna, an animal with exceptionally high mitochondrial content. In mice, an engineered mutation disrupting the PPARGC1A uORF increases PGC1 alpha protein levels and oxidative metabolism and confers protection from acute kidney injury. These studies identify a translational regulatory element governing oxidative metabolism and highlight its potential contribution to the evolution of organismal mitochondrial function.
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