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DNA损伤灶:含义与意义。

DNA damage foci: Meaning and significance.

作者信息

Rothkamm Kai, Barnard Stephen, Moquet Jayne, Ellender Michele, Rana Zohaib, Burdak-Rothkamm Susanne

机构信息

Public Health England, Centre for Radiation, Chemical and Environmental Hazards, Chilton, United Kingdom.

Department of Radiotherapy, Laboratory of Radiation Biology and Experimental Radiation Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Environ Mol Mutagen. 2015 Jul;56(6):491-504. doi: 10.1002/em.21944. Epub 2015 Mar 12.

Abstract

The discovery of DNA damage response proteins such as γH2AX, ATM, 53BP1, RAD51, and the MRE11/RAD50/NBS1 complex, that accumulate and/or are modified in the vicinity of a chromosomal DNA double-strand break to form microscopically visible, subnuclear foci, has revolutionized the detection of these lesions and has enabled studies of the cellular machinery that contributes to their repair. Double-strand breaks are induced directly by a number of physical and chemical agents, including ionizing radiation and radiomimetic drugs, but can also arise as secondary lesions during replication and DNA repair following exposure to a wide range of genotoxins. Here we aim to review the biological meaning and significance of DNA damage foci, looking specifically at a range of different settings in which such markers of DNA damage and repair are being studied and interpreted.

摘要

诸如γH2AX、ATM、53BP1、RAD51以及MRE11/RAD50/NBS1复合物等DNA损伤反应蛋白的发现,彻底改变了对这些损伤的检测方式,并使得对参与其修复的细胞机制的研究成为可能。这些蛋白在染色体DNA双链断裂附近积累和/或发生修饰,形成显微镜下可见的亚核灶。双链断裂可由多种物理和化学因素直接诱导产生,包括电离辐射和放射模拟药物,但在暴露于多种基因毒素后进行复制和DNA修复过程中也可能作为继发性损伤出现。在此,我们旨在综述DNA损伤灶的生物学意义,特别关注一系列正在研究和解释此类DNA损伤与修复标志物的不同情况。

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