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过氧化氢诱导的高阶染色质降解:氧化遗传毒性的一种新机制。

H2O2-induced higher order chromatin degradation: a novel mechanism of oxidative genotoxicity.

作者信息

Konat Gregory W

机构信息

Department of Neurobiology and Anatomy, West Virginia University School of Medicine, 4052 HSN, PO Box 9128 Morgantown, WV 26506-9128, USA.

出版信息

J Biosci. 2003 Feb;28(1):57-60. doi: 10.1007/BF02970132.

Abstract

The genotoxicity of reactive oxygen species (ROS) is well established. The underlying mechanism involves oxidation of DNA by ROS. However, we have recently shown that hydrogen peroxide (H2O2), the major mediator of oxidative stress, can also cause genomic damage indirectly. Thus, H2O2 at pathologically relevant concentrations rapidly induces higher order chromatin degradation (HOCD), i.e. enzymatic excision of chromatin loops and their oligomers at matrix-attachment regions. The activation of endonuclease that catalyzes HOCD is a signalling event triggered specifically by H2O2. The activation is not mediated by an influx of calcium ions, but resting concentrations of intracellular calcium ions are required for the maintenance of the endonuclease in an active form. Although H2O2-induced HOCD can efficiently dismantle the genome leading to cell death, under sublethal oxidative stress conditions H2O2-induced HOCD may be the major source of somatic mutations.

摘要

活性氧(ROS)的遗传毒性已得到充分证实。其潜在机制涉及ROS对DNA的氧化作用。然而,我们最近发现,氧化应激的主要介质过氧化氢(H2O2)也可间接导致基因组损伤。因此,病理相关浓度的H2O2会迅速诱导高阶染色质降解(HOCD),即在基质附着区域对染色质环及其寡聚体进行酶切。催化HOCD的核酸内切酶的激活是由H2O2特异性触发的信号事件。该激活不是由钙离子内流介导的,但细胞内钙离子的静息浓度是维持核酸内切酶活性形式所必需的。尽管H2O2诱导的HOCD可有效破坏基因组导致细胞死亡,但在亚致死性氧化应激条件下,H2O2诱导的HOCD可能是体细胞突变的主要来源。

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