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酿酒酵母同源重组因子Rad54和Rad51在染色质重塑中的协同作用。

Synergistic action of the Saccharomyces cerevisiae homologous recombination factors Rad54 and Rad51 in chromatin remodeling.

作者信息

Kwon Youngho, Chi Peter, Roh Dong Hyun, Klein Hannah, Sung Patrick

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.

出版信息

DNA Repair (Amst). 2007 Oct 1;6(10):1496-506. doi: 10.1016/j.dnarep.2007.04.012. Epub 2007 Jun 4.

Abstract

Rad54, a member of the Swi2/Snf2 protein family, works in concert with the RecA-like recombinase Rad51 during the early and late stages of homologous recombination. Rad51 markedly enhances the activities of Rad54, including the induction of topological changes in DNA and the remodeling of chromatin structure. Reciprocally, Rad54 promotes Rad51-mediated DNA strand invasion with either naked or chromatinized DNA. Here, using various Saccharomyces cerevisiae rad51 and rad54 mutant proteins, mechanistic aspects of Rad54/Rad51-mediated chromatin remodeling are defined. Disruption of the Rad51-Rad54 complex leads to a marked attenuation of chromatin remodeling activity. Moreover, we present evidence that assembly of the Rad51 presynaptic filament represents an obligatory step in the enhancement of the chromatin remodeling reaction. Interestingly, we find a specific interaction of the N-terminal tail of histone H3 with Rad54 and show that the H3 tail interaction domain resides within the amino terminus of Rad54. These results suggest that Rad54-mediated chromatin remodeling coincides with DNA homology search by the Rad51 presynaptic filament and that this process is facilitated by an interaction of Rad54 with histone H3.

摘要

Rad54是Swi2/Snf2蛋白家族的成员之一,在同源重组的早期和晚期与RecA样重组酶Rad51协同发挥作用。Rad51显著增强Rad54的活性,包括诱导DNA拓扑结构变化和重塑染色质结构。反过来,Rad54促进Rad51介导的裸DNA或染色质化DNA的DNA链侵入。在此,我们使用各种酿酒酵母rad51和rad54突变蛋白,定义了Rad54/Rad51介导的染色质重塑的机制方面。Rad51-Rad54复合物的破坏导致染色质重塑活性显著减弱。此外,我们提供的证据表明,Rad51突触前细丝的组装是增强染色质重塑反应的一个必要步骤。有趣的是,我们发现组蛋白H3的N端尾巴与Rad54存在特异性相互作用,并表明H3尾巴相互作用结构域位于Rad54的氨基末端内。这些结果表明,Rad54介导的染色质重塑与Rad51突触前细丝的DNA同源性搜索同时发生,并且这一过程通过Rad54与组蛋白H3的相互作用而得到促进。

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