Rothkamm Kai, Barnard Stephen, Moquet Jayne, Ellender Michele, Rana Zohaib, Burdak-Rothkamm Susanne
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.
Environ Mol Mutagen. 2015 Jul;56(6):491-504. doi: 10.1002/em.21944. Epub 2015 Mar 12.
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.
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。