尿素循环
锡尔图因
热卡限制
生物化学
酶
化学
线粒体
生物
NAD+激酶
内分泌学
氨基酸
精氨酸
作者
Takashi Nakagawa,Leonard Guarente
出处
期刊:Aging
[Impact Journals LLC]
日期:2009-06-29
卷期号:1 (6): 578-581
被引量:75
标识
DOI:10.18632/aging.100062
摘要
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.
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