CRL4Cdt2-Mediated Destruction of the Histone Methyltransferase Set8 Prevents Premature Chromatin Compaction in S Phase

被引:180
作者
Centore, Richard C. [1 ]
Havens, Courtney G. [3 ]
Manning, Amity L. [1 ]
Li, Ju-Mei [4 ]
Flynn, Rachel Litman [1 ]
Tse, Alice [1 ]
Jin, Jianping [4 ]
Dyson, Nicholas J. [1 ]
Walter, Johannes C. [3 ]
Zou, Lee [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Univ Texas Hlth Sci Ctr Houston, Dept Biochem & Mol Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
CELL NUCLEAR ANTIGEN; UBIQUITIN LIGASE COMPLEX; H4; LYSINE; 20; DNA-DAMAGE; CDT1; DEGRADATION; GENOME INTEGRITY; REPLICATION; METHYLATION; STABILITY; PCNA;
D O I
10.1016/j.molcel.2010.09.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 H4K20mel 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.
引用
收藏
页码:22 / 33
页数:12
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