Shifts in Replication Timing Actively Affect Histone Acetylation during Nucleosome Reassembly

被引:63
作者
Lande-Diner, Laura [1 ]
Zhang, Jianmin [1 ]
Cedar, Howard [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Inst Med Res Israel Canada, Dept Dev Biol & Canc Res, IL-91120 Jerusalem, Israel
基金
以色列科学基金会;
关键词
CHROMATIN-STRUCTURE; GENE; DNA; TRANSCRIPTION; ORGANIZATION; METHYLATION; CHROMOSOME; RESOLUTION; PROFILE; GENOME;
D O I
10.1016/j.molcel.2009.05.027
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 entire genome is replicated in a programmed manner, with specific regions undergoing DNA synthesis at different times in S phase. Active genes generally replicate in early S phase, while repressed genes replicate late, and for some loci this process is developmentally regulated. Using a nuclear microinjection system, we demonstrate that DNA sequences originally packaged into nucleosomes containing deacetylated histones during late S become reassembled with acetylated histones after undergoing replication in early S. Conversely, a change from early to late replication timing is accompanied by repackaging into nucleosomes containing deacetylated histones. This is carried out by differential cell-cycle-controlled acetylation and deacetylation of histones H3 and H4. These studies provide strong evidence that switches in replication timing may play a role in the regulation of nucleosome structure during development.
引用
收藏
页码:767 / 774
页数:8
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