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The anaphase promoting complex promotes NHEJ repair through stabilizing Ku80 at DNA damage sites

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Version 2 2021-09-29, 12:34
Version 1 2018-06-13, 04:37
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posted on 2021-09-29, 12:34 authored by Chengxian Ma, Kyungsoo Ha, Min-su Kim, Young-Woock Noh, Han Lin, Lichun Tang, Qing Zhu, Dan Zhang, Huan Chen, Suxia Han, Pumin Zhang

Double-strand breaks (DSBs) are repaired through two major pathways, homology-directed recombination (HDR) and non-homologous end joining (NHEJ). The choice between these two pathways is largely influenced by cell cycle phases. HDR can occur only in S/G2 when sister chromatid can provide homologous templates, whereas NHEJ can take place in all phases of the cell cycle except mitosis. Central to NHEJ repair is the Ku70/80 heterodimer which forms a ring structure that binds DSB ends and serves as a platform to recruit factors involved in NHEJ. Upon completion of NHEJ repair, DNA double strand-encircling Ku dimers have to be removed. The removal depends on ubiquitylation and proteasomal degradation of Ku80 by the ubiquitin E3 ligases RNF8. Here we report that RNF8 is a substrate of APCCdh1 and the latter keeps RNF8 level in check at DSBs to prevent premature turnover of Ku80.

Funding

This work was supported in part by a Chinese National Natural Science Foundation grant (# 81773032) and in part by an international collaboration grant (# 2013DFB30210) and a 973 Project grant (# 2013CB910300) from Chinese Minister of Science and Technology. PZ is supported by grants from NIH (CA116097 and CA122623). S.H. is supported by grants (# 81272488, 81472795, 81602802 and 81602680) from Chinese National Natural Science Foundation. Y.N. and M.K. are supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIP) (NRF-2016R1A6A3A04011000). We also thank other members of the Zhang lab for helpful discussion and support.

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