4.8 Article

The TFEB orthologue HLH-30 regulates autophagy and modulates longevity in Caenorhabditis elegans

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NATURE COMMUNICATIONS
卷 4, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms3267

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资金

  1. NIH/UCSD [P50 AG005131-29]
  2. Glenn Foundation for Aging Research fellowship
  3. Fund for Medical Discovery postdoctoral fellowship from the Massachusetts General Hospital
  4. NIH/NIA [F31 AG039222, R01 AG027463, R01 AG038664, R01 AG039756]
  5. NIH/NIGMS [R01 GM101056]

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Autophagy is a cellular recycling process that has an important anti-aging role, but the underlying molecular mechanism is not well understood. The mammalian transcription factor EB (TFEB) was recently shown to regulate multiple genes in the autophagy process. Here we show that the predicted TFEB orthologue HLH-30 regulates autophagy in Caenorhabditis elegans and, in addition, has a key role in lifespan determination. We demonstrate that hlh-30 is essential for the extended lifespan of Caenorhabditis elegans in six mechanistically distinct longevity models, and overexpression of HLH-30 extends lifespan. Nuclear localization of HLH-30 is increased in all six Caenorhabditis elegans models and, notably, nuclear TFEB levels are augmented in the livers of mice subjected to dietary restriction, a known longevity-extending regimen. Collectively, our results demonstrate a conserved role for HLH-30 and TFEB in autophagy, and possibly longevity, and identify HLH-30 as a uniquely important transcription factor for lifespan modulation in Caenorhabditis elegans.

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