4.7 Article

The Rieske oxygenase DAF-36 functions as a cholesterol 7-desaturase in steroidogenic pathways governing longevity

期刊

AGING CELL
卷 10, 期 5, 页码 879-884

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1474-9726.2011.00733.x

关键词

bile acid; nuclear receptor; endocrine signaling; hormone; development; aging

资金

  1. NIA [RO1AG027498]
  2. Max Planck Society
  3. Howard Hughes Medical Foundation, NIH [U19DK62434]
  4. Welch Foundation
  5. Natural Sciences and Engineering Research Council of Canada [356873-08]
  6. Canadian Institutes of Health Research [MOP-89361, 97904]
  7. Canada Foundation for Innovation

向作者/读者索取更多资源

Bile acids are cholesterol-derived signaling molecules that regulate mammalian metabolism through sterol-sensing nuclear receptor transcription factors. In C. elegans, bile acid-like steroids called dafachronic acids (DAs) control developmental timing and longevity by activating the nuclear receptor DAF-12. However, little is known about the biosynthesis of these molecules. Here, we show that the DAF-36/Rieske oxygenase works at the first committed step, converting cholesterol to 7-dehydrocholesterol. Its elucidation as a cholesterol 7-desaturase provides crucial biochemical evidence that such oxygenases are key steroidogenic enzymes. By controlling DA production, DAF-36 regulates DAF-12 activities for reproductive development and longevity and may illuminate related pathways in metazoans.

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