| Literature DB >> 33797206 |
Jessica Kelliher1, Gargi Ghosal2, Justin Wai Chung Leung1.
Abstract
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.Entities:
Keywords: DNA double-strand break; DNA repair; RIDDLE syndrome; RIDDLIN; ubiquitin
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Year: 2021 PMID: 33797206 PMCID: PMC8486888 DOI: 10.1111/febs.15857
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.622