Epigenomic Medicine, BakerIDI Heart and Diabetes Institute, The Alfred Medical Research and Education Precinct, Melbourne, Victoria, Australia.
Leukemia. 2010 Apr;24(4):679-86. doi: 10.1038/leu.2010.6. Epub 2010 Feb 4.
Phosphorylation of the Ser-139 residue of the histone variant H2AX, forming gammaH2AX, is an early cellular response to the induction of DNA double-strand breaks. Detection of this phosphorylation event has emerged as a highly specific and sensitive molecular marker for monitoring DNA damage initiation and resolution. Further, analysis of gammaH2AX foci has numerous other applications including, but not limited to, cancer and aging research. Quantitation of gammaH2AX foci has also been applied as a useful tool for the evaluation of the efficacy of various developmental drugs, particularly, radiation modifying compounds. This review focuses on the current status of gammaH2AX as a marker of DNA damage and repair in the context of ionizing radiation. Although the emphasis is on gamma-radiation-induced gammaH2AX foci, the effects of other genotoxic insults including exposure to ultraviolet rays, oxidative stress and chemical agents are also discussed.
组蛋白变体 H2AX 的丝氨酸 139 残基的磷酸化形成 γH2AX,是细胞对 DNA 双链断裂诱导的早期反应。这种磷酸化事件的检测已成为监测 DNA 损伤起始和修复的高度特异性和敏感的分子标记。此外,γH2AX 焦点分析还有许多其他应用,包括但不限于癌症和衰老研究。γH2AX 焦点的定量也被用作评估各种发育药物(特别是辐射修饰化合物)疗效的有用工具。本综述重点介绍了 γH2AX 作为电离辐射条件下 DNA 损伤和修复标志物的现状。虽然重点是 γ 射线诱导的 γH2AX 焦点,但也讨论了其他遗传毒性刺激物,包括紫外线照射、氧化应激和化学试剂的影响。