Crampton Amber, Chang FuJung, Pappas Donald L, Frisch Ryan L, Weinreich Michael
Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
Mol Cell. 2008 Apr 25;30(2):156-66. doi: 10.1016/j.molcel.2008.02.019.
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, I(S) elements occurred within positioned nucleosomes, and Abf1p-mediated exclusion of nucleosomes from the origin abrogated the inhibition. These data suggest that Sir2p and I(S) elements inhibit origin activity by promoting an unfavorable chromatin structure for pre-RC assembly.
在G1期,一个决定DNA合成起始位置的复制前复合体(pre-RC)在起始点形成。Sir2p组蛋白去乙酰化酶在一部分起始点抑制pre-RC组装,这表明Sir2p通过起始点结构的独特方面来抑制DNA复制。在这里,我们在III号和VI号染色体上鉴定出五个对SIR2敏感的起始点。对两个起始点的连接子扫描分析表明它们具有共同的组织架构,包括一个位于起始点识别复合体(ORC)结合位点和pre-RC组装位点3'端的抑制序列。这个抑制序列(I(S))的活性需要SIR2,这表明Sir2p通过该序列抑制起始点。此外,I(S)元件出现在定位核小体内部,并且Abf1p介导的核小体从起始点的排除消除了这种抑制作用。这些数据表明Sir2p和I(S)元件通过促进不利于pre-RC组装的染色质结构来抑制起始点活性。