Department of Radiation Oncology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
FEBS J. 2022 May;289(9):2467-2480. doi: 10.1111/febs.15857. Epub 2021 Apr 16.
The chromatin-based DNA damage response pathway is tightly orchestrated by histone post-translational modifications, including histone H2A ubiquitination. Ubiquitination plays an integral role in regulating cellular processes including DNA damage signaling and repair. The ubiquitin E3 ligase RNF168 is essential in assembling a cohort of DNA repair proteins at the damaged chromatin via its enzymatic activity. RNF168 ubiquitinates histone H2A(X) at the N terminus and generates a specific docking scaffold for ubiquitin-binding motif-containing proteins. The regulation of RNF168 at damaged chromatin and the mechanistic implication in the recruitment of DNA repair proteins to the damaged sites remain an area of active investigation. Here, we review the function and regulation of RNF168 in the context of ubiquitin-mediated DNA damage signaling and repair. We will also discuss the unanswered questions that require further investigation and how understanding RNF168 targeting specificity could benefit the therapeutic development for cancer treatment.
基于染色质的 DNA 损伤反应途径受到组蛋白翻译后修饰的严格调控,包括组蛋白 H2A 的泛素化。泛素化在调节细胞过程中起着重要作用,包括 DNA 损伤信号转导和修复。泛素 E3 连接酶 RNF168 通过其酶活性在受损染色质上组装一组 DNA 修复蛋白。RNF168 在 N 端泛素化组蛋白 H2A(X),并为含有泛素结合基序的蛋白质生成特定的对接支架。RNF168 在受损染色质上的调节以及在将 DNA 修复蛋白募集到受损部位的机制意义仍然是一个活跃的研究领域。在这里,我们将综述 RNF168 在泛素介导的 DNA 损伤信号转导和修复中的功能和调节。我们还将讨论需要进一步研究的未解决问题,以及了解 RNF168 靶向特异性如何有益于癌症治疗的治疗发展。