An ARS element inhibits DNA replication through a SIR2-Dependent mechanism

被引:56
作者
Crampton, Amber [1 ,2 ]
Chang, FuJung [1 ]
Pappas, Donald L., Jr. [1 ]
Frisch, Ryan L. [1 ]
Weinreich, Michael [1 ]
机构
[1] Van Andel Res Inst, Lab Chromosome Replicat, Grand Rapids, MI 49503 USA
[2] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
关键词
D O I
10.1016/j.molcel.2008.02.019
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
During G1 phase, a prereplicative complex (pre-RC) that determines where DNA synthesis initiates forms at origins. The Sir2p histone deacetylase inhibits pre-RC assembly at a subset of origins, suggesting that Sir2p, inhibits DNA replication through a unique aspect of origin structure. Here, we identified five SIR2-sensitive origins on chromosomes III and VI . Linker scan analysis of two origins indicated that they share a common organization, including an inhibitory sequence positioned 3' to the sites of origin recognition complex (ORC) binding and pre-RC assembly. This inhibitory sequence (I-s) required SIR2 for its activity, suggesting that SIR2 inhibits origins through this sequence. Furthermore, Is elements occurred within positioned nucleosomes, and Abf1 p-mediated exclusion of nucleosomes from the origin abrogated the inhibition. These data suggest that Sir2p, and Is elements inhibit origin activity by promoting an unfavorable chromatin structure for pre-RC assembly.
引用
收藏
页码:156 / 166
页数:11
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