首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Mitochondrial Protein Acylation and Intermediary Metabolism: Regulation by Sirtuins and Implications for Metabolic Disease
【2h】

Mitochondrial Protein Acylation and Intermediary Metabolism: Regulation by Sirtuins and Implications for Metabolic Disease

机译:线粒体蛋白酰化和中间代谢:Sirtuins的调节及其对代谢性疾病的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:sirtuins是一类NAD + 依赖性蛋白脱乙酰酶,可调节细胞存活,代谢和寿命。三个sirtuins,SIRT3-5,定位于线粒体。在禁食和卡路里限制期间,SIRT3的表达被选择性激活。 SIRT3调节关键代谢酶(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)的乙酰化水平和酶活性,并增强禁食期间的脂肪代谢。 SIRT5表现出去丙二酸化酶/去琥珀酸化酶活性,并且赖氨酸琥珀酰化和丙二酰化是丰富的线粒体蛋白修饰。对于SIRT4,没有令人信服的酶活性报道。在这里,我们回顾了线粒体sirtuins作为代谢传感器的新兴作用,它们响应细胞能量状态的变化并通过蛋白质脱酰作用调节关键代谢酶的活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号