Suppr超能文献

植物组蛋白修饰对 DNA 损伤的响应动力学。

Dynamics of plant histone modifications in response to DNA damage.

机构信息

Centre for Plant Sciences, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, UK.

出版信息

Biochem J. 2012 Aug 1;445(3):393-401. doi: 10.1042/BJ20111956.

Abstract

DNA damage detection and repair take place in the context of chromatin, and histone proteins play important roles in these events. Post-translational modifications of histone proteins are involved in repair and DNA damage signalling processes in response to genotoxic stresses. In particular, acetylation of histones H3 and H4 plays an important role in the mammalian and yeast DNA damage response and survival under genotoxic stress. However, the role of post-translational modifications to histones during the plant DNA damage response is currently poorly understood. Several different acetylated H3 and H4 N-terminal peptides following X-ray treatment were identified using MS analysis of purified histones, revealing previously unseen patterns of histone acetylation in Arabidopsis. Immunoblot analysis revealed an increase in the relative abundance of the H3 acetylated N-terminus, and a global decrease in hyperacetylation of H4 in response to DNA damage induced by X-rays. Conversely, mutants in the key DNA damage signalling factor ATM (ATAXIA TELANGIECTASIA MUTATED) display increased histone acetylation upon irradiation, linking the DNA damage response with dynamic changes in histone modification in plants.

摘要

DNA 损伤检测和修复发生在染色质的背景下,组蛋白在这些事件中发挥着重要作用。组蛋白蛋白的翻译后修饰参与了修复和 DNA 损伤信号转导过程,以应对遗传毒性应激。特别是组蛋白 H3 和 H4 的乙酰化在哺乳动物和酵母的 DNA 损伤反应以及遗传毒性应激下的存活中起着重要作用。然而,在植物 DNA 损伤反应过程中组蛋白翻译后修饰的作用目前知之甚少。使用纯化组蛋白的 MS 分析鉴定了 X 射线处理后几种不同的乙酰化 H3 和 H4 N 端肽,揭示了拟南芥中以前未见过的组蛋白乙酰化模式。免疫印迹分析显示,H3 乙酰化 N 端的相对丰度增加,而 X 射线诱导的 DNA 损伤导致 H4 的过度乙酰化全局减少。相反,关键的 DNA 损伤信号因子 ATM(共济失调毛细血管扩张突变)的突变体在辐照后显示出组蛋白乙酰化增加,将 DNA 损伤反应与植物中组蛋白修饰的动态变化联系起来。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验