首页> 美国卫生研究院文献>BioMed Research International >Sirtuins: Molecular Traffic Lights in the Crossroad of Oxidative Stress Chromatin Remodeling and Transcription
【2h】

Sirtuins: Molecular Traffic Lights in the Crossroad of Oxidative Stress Chromatin Remodeling and Transcription

机译:Sirtuins:氧化应激染色质重塑和转录的十字路口的分子交通灯。

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

Transcription is regulated by acetylation/deacetylation reactions of histone and nonhistone proteins mediated by enzymes called KATs and HDACs, respectively. As a major mechanism of transcriptional regulation, protein acetylation is a key controller of physiological processes such as cell cycle, DNA damage response, metabolism, apoptosis, and autophagy. The deacetylase activity of class III histone deacetylases or sirtuins depends on the presence of NAD+ (nicotinamide adenine dinucleotide), and therefore, their function is closely linked to cellular energy consumption. This activity of sirtuins connects the modulation of chromatin dynamics and transcriptional regulation under oxidative stress to cellular lifespan, glucose homeostasis, inflammation, and multiple aging-related diseases including cancer. Here we provide an overview of the recent developments in relation to the diverse biological activities associated with sirtuin enzymes and stress responsive transcription factors, DNA damage, and oxidative stress and relate the involvement of sirtuins in the regulation of these processes to oncogenesis. Since the majority of the molecular mechanisms implicated in these pathways have been described for Sirt1, this sirtuin family member is more extensively presented in this paper.
机译:转录分别受称为KAT和HDAC的酶介导的组蛋白和非组蛋白的乙酰化/脱乙酰化反应调节。作为转录调控的主要机制,蛋白质乙酰化是诸如细胞周期,DNA损伤反应,代谢,细胞凋亡和自噬等生理过程的关键控制器。 III类组蛋白脱乙酰基酶或sirtuins的脱乙酰基酶活性取决于NAD + (烟酰胺腺嘌呤二核苷酸)的存在,因此它们的功能与细胞能量消耗密切相关。沉默调节蛋白的这种活性将氧化应激下的染色质动力学调节和转录调控与细胞寿命,葡萄糖稳态,炎症以及包括癌症在内的多种与衰老相关的疾病联系在一起。在这里,我们概述了与瑟土因酶和应激反应转录因子,DNA损伤和氧化应激有关的多种生物活性有关的最新进展,并将瑟土因在这些过程的调控中与肿瘤发生联系起来。由于已针对Sirt1描述了与这些途径有关的大多数分子机制,因此在本文中将更广泛地介绍这种sirtuin家族成员。

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