Urea cycle regulation by mitochondrial sirtuin, SIRT5.

Takashi Nakagawa*, Leonard Guarente

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

60 被引用数 (Scopus)

抄録

Mammalian sirtuins have diverse roles in aging, metabolism and disease. Recently we reported a new function for SIRT5 in urea cycle regulation. Our study uncovered that SIRT5 localized to mitochondria matrix and deacetylates carbamoyl phosphate synthetase 1 (CPS1), an enzyme which is the first and rate-limiting step of urea cycle. Deacetylation of CPS1 by SIRT5 resulted in activation of CPS1 enzymatic activity. Indeed, SIRT5-deficient mice failed to up-regulate CPS1 activity and showed hyper ammonemia during fasting. Similar effects are also observed on high protein diet or calorie restriction. These data indicate SIRT5 also has an emerging role in the metabolic adaptation to fasting, high protein diet and calorie restriction.

本文言語英語
ページ(範囲)578-581
ページ数4
ジャーナルAging
1
6
DOI
出版ステータス出版済み - 2009/06

ASJC Scopus 主題領域

  • 加齢科学
  • 細胞生物学

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