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.
| Original language | English |
|---|---|
| Pages (from-to) | 1138-1145 |
| Number of pages | 8 |
| Journal | Cell Cycle |
| Volume | 17 |
| Issue number | 9 |
| DOIs | |
| State | Published - 3 May 2018 |
| Externally published | Yes |
Keywords
- Anaphase promoting complex
- Cdh1
- NHEJ repair
- RNF8
- double-strand breaks
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