Department of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 06974, Korea.
BMB Rep. 2022 Nov;55(11):541-546. doi: 10.5483/BMBRep.2022.55.11.080.
The repair of DNA double-strand breaks (DSBs) by homologous recombination (HR) is crucial for maintaining genomic integrity and is involved in numerous fundamental biological processes. Post-translational modifications by proteins play an important role in regulating DNA repair. Here, we report that the methyltransferase SET7 regulates HR-mediated DSB repair by methylating TIP60, a histone acetyltransferase and tumor suppressor involved in gene expression and protein stability. We show that SET7 targets TIP60 for methylation at K137, which facilitates DSB repair by promoting HR and determines cell viability against DNA damage. Interestingly, TIP60 demethylation is catalyzed by LSD1, which affects HR efficiency. Taken together, our findings reveal the importance of TIP60 methylation status by SET7 and LSD1 in the DSB repair pathway. [BMB Reports 2022; 55(11): 541-546].
DNA 双链断裂(DSBs)的同源重组(HR)修复对于维持基因组完整性至关重要,并且涉及许多基本的生物学过程。蛋白质的翻译后修饰在调节 DNA 修复中起着重要作用。在这里,我们报告说,甲基转移酶 SET7 通过甲基化 TIP60 来调节 HR 介导的 DSB 修复,TIP60 是一种组蛋白乙酰转移酶和肿瘤抑制因子,参与基因表达和蛋白质稳定性。我们表明,SET7 将 TIP60 靶向 K137 进行甲基化,这通过促进 HR 促进 DSB 修复,并决定细胞对 DNA 损伤的存活能力。有趣的是,LSD1 催化 TIP60 的去甲基化,这影响 HR 效率。总之,我们的研究结果揭示了 SET7 和 LSD1 对 DSB 修复途径中 TIP60 甲基化状态的重要性。[BMB 报告 2022;55(11): 541-546]。