Department of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht, Utrecht, The Netherlands.
Oncogene. 2010 Apr 15;29(15):2281-91. doi: 10.1038/onc.2009.501. Epub 2010 Jan 25.
DNA double-stranded breaks (DSBs) elicit a checkpoint response that causes a delay in cell cycle progression. Early in the checkpoint response, histone H2AX is phosphorylated in the chromatin region flanking the DSB by ATM/ATR and DNA-PK kinases. The resulting foci of phosphorylated H2AX (gamma-H2AX) serve as a platform for recruitment and retention of additional components of the checkpoint-signaling cascade that enhance checkpoint signaling and DSB repair. Upon repair, both the assembled protein complexes and the chromatin modifications are removed to quench the checkpoint signal. In this study, we show that the DNA damage-responsive Wip1 phosphatase is bound to chromatin. Moreover, Wip1 directly dephosphorylates gamma-H2AX and cells depleted of Wip1 fail to dephosphorylate gamma-H2AX during checkpoint recovery. Conversely, premature activation of Wip1 leads to displacement of MDC1 from damage foci and prevents activation of the checkpoint. Taken together, our data show that Wip1 has an essential role in dephosphorylation of gamma-H2AX to silence the checkpoint and restore chromatin structure once DNA damage is repaired.
DNA 双链断裂(DSBs)会引发一个检查点反应,导致细胞周期进程的延迟。在检查点反应的早期,ATM/ATR 和 DNA-PK 激酶会在 DSB 侧翼的染色质区域将组蛋白 H2AX 磷酸化。磷酸化的 H2AX(γ-H2AX)形成的焦点作为检查点信号级联中其他成分的募集和保留的平台,从而增强检查点信号和 DSB 修复。在修复后,组装的蛋白质复合物和染色质修饰都会被去除,以消除检查点信号。在这项研究中,我们表明,对 DNA 损伤有反应的 Wip1 磷酸酶与染色质结合。此外,Wip1 可直接使 γ-H2AX 去磷酸化,而耗尽 Wip1 的细胞在检查点恢复过程中无法使 γ-H2AX 去磷酸化。相反,过早激活 Wip1 会导致 MDC1 从损伤焦点中移位,并阻止检查点的激活。总之,我们的数据表明,Wip1 在去磷酸化 γ-H2AX 以沉默检查点并在修复 DNA 损伤后恢复染色质结构方面发挥着重要作用。