Department of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.
Int J Mol Sci. 2022 Aug 29;23(17):9780. doi: 10.3390/ijms23179780.
In response to DNA damage, cells have developed a sophisticated signaling pathway, consisting of DNA damage sensors, transducers, and effectors, to ensure efficient and proper repair of damaged DNA. During this process, posttranslational modifications (PTMs) are central events that modulate the recruitment, dissociation, and activation of DNA repair proteins at damage sites. Emerging evidence reveals that protein arginine methylation is one of the common PTMs and plays critical roles in DNA damage response. Protein arginine methyltransferases (PRMTs) either directly methylate DNA repair proteins or deposit methylation marks on histones to regulate their transcription, RNA splicing, protein stability, interaction with partners, enzymatic activities, and localization. In this review, we summarize the substrates and roles of each PRMTs in DNA damage response and discuss the synergistic anticancer effects of PRMTs and DNA damage pathway inhibitors, providing insight into the significance of arginine methylation in the maintenance of genome integrity and cancer therapies.
针对 DNA 损伤,细胞已开发出一种复杂的信号通路,包括 DNA 损伤传感器、转导器和效应器,以确保受损 DNA 的有效和适当修复。在此过程中,翻译后修饰(PTMs)是调节损伤部位 DNA 修复蛋白募集、解离和激活的核心事件。新出现的证据表明,蛋白质精氨酸甲基化是常见的 PTM 之一,在 DNA 损伤反应中发挥关键作用。蛋白质精氨酸甲基转移酶(PRMTs)要么直接甲基化 DNA 修复蛋白,要么在组蛋白上沉积甲基化标记,以调节其转录、RNA 剪接、蛋白质稳定性、与伴侣的相互作用、酶活性和定位。在这篇综述中,我们总结了每种 PRMT 在 DNA 损伤反应中的底物和作用,并讨论了 PRMT 和 DNA 损伤途径抑制剂的协同抗癌作用,为精氨酸甲基化在维持基因组完整性和癌症治疗中的意义提供了深入了解。