| Literature DB >> 29895199 |
Chengxian Ma1, Kyungsoo Ha2,3,4, Min-Su Kim4, Young-Woock Noh4, Han Lin3, Lichun Tang2, Qing Zhu5, Dan Zhang1, Huan Chen2, Suxia Han1, Pumin Zhang2,3.
Abstract
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.Entities:
Keywords: Anaphase promoting complex; Cdh1; NHEJ repair; RNF8; double-strand breaks
Year: 2018 PMID: 29895199 PMCID: PMC6110584 DOI: 10.1080/15384101.2018.1464836
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534