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一个自主复制序列元件通过一种依赖SIR2的机制抑制DNA复制。

An ARS element inhibits DNA replication through a SIR2-dependent mechanism.

作者信息

Crampton Amber, Chang FuJung, Pappas Donald L, Frisch Ryan L, Weinreich Michael

机构信息

Laboratory of Chromosome Replication, Van Andel Research Institute, Grand Rapids, MI 49503, USA.

出版信息

Mol Cell. 2008 Apr 25;30(2):156-66. doi: 10.1016/j.molcel.2008.02.019.

Abstract

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.

摘要

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。

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