| Literature DB >> 20932472 |
Richard C Centore1, Courtney G Havens, Amity L Manning, Ju-Mei Li, Rachel Litman Flynn, Alice Tse, Jianping Jin, Nicholas J Dyson, Johannes C Walter, Lee Zou.
Abstract
The proper coordination between DNA replication and mitosis during cell-cycle progression is crucial for genomic stability. During G2 and mitosis, Set8 catalyzes monomethylation of histone H4 on lysine 20 (H4K20me1), which promotes chromatin compaction. Set8 levels decline in S phase, but why and how this occurs is unclear. Here, we show that Set8 is targeted for proteolysis in S phase and in response to DNA damage by the E3 ubiquitin ligase, CRL4(Cdt2). Set8 ubiquitylation occurs on chromatin and is coupled to DNA replication via a specific degron in Set8 that binds PCNA. Inactivation of CRL4(Cdt2) leads to Set8 stabilization and aberrant H4K20me1 accumulation in replicating cells. Transient S phase expression of a Set8 mutant lacking the degron promotes premature H4K20me1 accumulation and chromatin compaction, and triggers a checkpoint-mediated G2 arrest. Thus, CRL4(Cdt2)-dependent destruction of Set8 in S phase preserves genome stability by preventing aberrant chromatin compaction during DNA synthesis.Entities:
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Year: 2010 PMID: 20932472 PMCID: PMC2957874 DOI: 10.1016/j.molcel.2010.09.015
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970