Bruinsma Wytse, van den Berg Jeroen, Aprelia Melinda, Medema René H
Department of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands Department of Medical Oncology and Cancer Genomics Center, University Medical Center Utrecht, Utrecht, The Netherlands.
Department of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
EMBO Rep. 2016 May;17(5):659-70. doi: 10.15252/embr.201540767. Epub 2016 Mar 1.
In order to maintain a stable genome, cells need to detect and repair DNA damage before they complete the division cycle. To this end, cell cycle checkpoints prevent entry into the next cell cycle phase until the damage is fully repaired. Proper reentry into the cell cycle, known as checkpoint recovery, requires that a cell retains its original cell cycle state during the arrest. Here, we have identified Tousled-like kinase 2 (Tlk2) as an important regulator of recovery after DNA damage in G2. We show that Tlk2 regulates the Asf1A histone chaperone in response to DNA damage and that depletion of Asf1A also produces a recovery defect. Both Tlk2 and Asf1A are required to restore histone H3 incorporation into damaged chromatin. Failure to do so affects expression of pro-mitotic genes and compromises the cellular competence to recover from damage-induced cell cycle arrests. Our results demonstrate that Tlk2 promotes Asf1A function during the DNA damage response in G2 to allow for proper restoration of chromatin structure at the break site and subsequent recovery from the arrest.
为了维持基因组的稳定性,细胞需要在完成分裂周期之前检测并修复DNA损伤。为此,细胞周期检查点会阻止细胞进入下一个细胞周期阶段,直到损伤完全修复。正确重新进入细胞周期,即所谓的检查点恢复,要求细胞在停滞期间保持其原始细胞周期状态。在此,我们已确定类Tousled激酶2(Tlk2)是G2期DNA损伤后恢复的重要调节因子。我们表明,Tlk2响应DNA损伤调节Asf1A组蛋白伴侣,并且Asf1A的缺失也会产生恢复缺陷。Tlk2和Asf1A都是将组蛋白H3掺入受损染色质所必需的。如果做不到这一点,会影响促有丝分裂基因的表达,并损害细胞从损伤诱导的细胞周期停滞中恢复的能力。我们的结果表明,Tlk2在G2期的DNA损伤反应中促进Asf1A的功能,以便在断裂位点正确恢复染色质结构,并随后从停滞中恢复。