Acetylation of 53BP1 dictates the DNA double strand break repair pathway

作者：Guo, Xiang; Bai, Yongtai; Zhao, Meimei; Zhou, Mei; Shen, Qinjian; Yun, Cai-Hong; Zhang, Hongquan; Zhu, Wei-Guo; Wang, Jiadong^*

来源：Nucleic Acids Research, 2018, 46(2): 689-703.

DOI：10.1093/nar/gkx1208

• DAMAGE RESPONSE
• END RESECTION
• HOMOLOGOUS RECOMBINATION
• NUCLEOSOME RECOGNITION
• REGULATES 53BP1
• DSB REPAIR
• CHROMATIN
• UBIQUITIN
• RECRUITMENT
• BINDING

P53-binding protein 1 (53BP1) plays critical roles in DNA double strand break (DSB) repair by promoting non-homologous end joining (NHEJ), and loss of 53BP1 abolishes PARPi sensitivity in BRCA1deficient cells by restoring homologous recombination (HR). 53BP1 is one of the proteins initially recruited to sites of DSBs via recognition of H4K20me2 through the Tudor-UDR domain and H2AK15ub through the UDR motif. Although extensive studies have been conducted, it remains unclear how the post-translational modification of 53BP1 affects DSB repair pathway choice. Here, we identified 53BP1 as an acetylated protein and determined that acetylation of 53BP1 inhibit NHEJ and promote HR by negatively regulating 53BP1 recruitment to DSBs. Mechanistically, CBP-mediated acetylation of K1626/1628 in the UDR motif disrupted the interaction between 53BP1 and nucleosomes, subsequently blocking the recruitment of 53BP1 and its downstream factors PTIP and RIF1 to DSBs. Hyperacetylation of 53BP1, similar to depletion of 53BP1, restored PARPi resistance in BRCA1-deficient cells. Interestingly, 53BP1 acetylation was tightly regulated by HDAC2 to maintain balance between the HR and NHEJ pathways. Together, our results demonstrate that the acetylation status of 53BP1 plays a key role in its recruitment to DSBs and reveal how specific 53BP1 modification modulates the choice of DNA repair pathway.

• 出版日期2018-1-25
• 单位深圳大学; 北京大学