线粒体蛋白酰化和中间代谢:沉默信息调节因子和代谢性疾病的影响

Mitochondrial protein acylation and intermediary metabolism: regulation by sirtuins and implications for metabolic disease.

机构信息

Gladstone Institute of Virology and Immunology, San Francisco, California 94158, USA.

出版信息

J Biol Chem. 2012 Dec 14;287(51):42436-43. doi: 10.1074/jbc.R112.404863. Epub 2012 Oct 18.

Abstract

The sirtuins are a family of NAD(+)-dependent protein deacetylases that regulate cell survival, metabolism, and longevity. Three sirtuins, SIRT3-5, localize to mitochondria. Expression of SIRT3 is selectively activated during fasting and calorie restriction. SIRT3 regulates the acetylation level and enzymatic activity of key metabolic enzymes, such as acetyl-CoA synthetase, long-chain acyl-CoA dehydrogenase, and 3-hydroxy-3-methylglutaryl-CoA synthase 2, and enhances fat metabolism during fasting. SIRT5 exhibits demalonylase/desuccinylase activity, and lysine succinylation and malonylation are abundant mitochondrial protein modifications. No convincing enzymatic activity has been reported for SIRT4. Here, we review the emerging role of mitochondrial sirtuins as metabolic sensors that respond to changes in the energy status of the cell and modulate the activities of key metabolic enzymes via protein deacylation.

摘要

去乙酰化酶 sirtuins 是一组依赖烟酰胺腺嘌呤二核苷酸 (NAD(+)) 的蛋白去乙酰化酶,可调节细胞存活、代谢和寿命。三种 sirtuins(SIRT3-5)定位于线粒体。SIRT3 的表达在禁食和热量限制期间被选择性激活。SIRT3 调节关键代谢酶的乙酰化水平和酶活性,如乙酰辅酶 A 合成酶、长链酰基辅酶 A 脱氢酶和 3-羟基-3-甲基戊二酰辅酶 A 合酶 2,并增强禁食期间的脂肪代谢。SIRT5 表现出脱氨酶/脱琥珀酰酶活性,赖氨酸琥珀酰化和丙二酰化是丰富的线粒体蛋白修饰。尚未报道 SIRT4 的明确酶活性。在这里,我们回顾了线粒体 sirtuins 作为代谢传感器的新作用,它们可以响应细胞能量状态的变化,并通过蛋白去乙酰化来调节关键代谢酶的活性。

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