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枯草芽孢杆菌噬菌体SPP1的复制体组织者(G38P)与SPP1基因组的两个离散的远距离区域形成特殊的核蛋白复合物。

The replisome organizer (G38P) of Bacillus subtilis bacteriophage SPP1 forms specialized nucleoprotein complexes with two discrete distant regions of the SPP1 genome.

作者信息

Missich R, Weise F, Chai S, Lurz R, Pedré X, Alonso J C

机构信息

Campus Universidad Autónoma de Madrid Centro Nacional de Biotecnología, CSIC Cantoblanco, Spain.

出版信息

J Mol Biol. 1997 Jul 4;270(1):50-64. doi: 10.1006/jmbi.1997.1060.

DOI:10.1006/jmbi.1997.1060
PMID:9231900
Abstract

Initiation of Bacillus subtilis bacteriophage SPP1 DNA replication requires the products of genes 38, 39 and 40 (G38P, G39P and G40P). G38P specifically binds two discrete regions, which are 32.1 kb apart in a linear map of the SPP1 genome. One of these target sites, which maps at the left end of the phage genome, within gene 38, was shown to function as an origin of replication and was therefore termed left origin (oriL). The other site, which lies within a non-coding segment in the late transcribed region on the right end of the genome, was termed oriR. Both sites contain two types of repeated elements (termed Box AB and A + T-rich region). The K(app) for the G38P-oriL DNA and G38P-oriR DNA complexes was estimated to be 1 nM and 4 nM, respectively. G38P binds to the distant oriL and oriR sites cooperatively. DNase I footprinting experiments showed protection by G38P in Box AB, but not in the A + T-rich region. Electron microscopy analysis showed that G38P forms a higher-order nucleoprotein structure with the SPP1 oriL and oriR sites through protein-protein interaction. G38P binding at its cognate sites does not seem to modify the length of the DNA, but to bend it. These results suggest that G38P forms a nucleoprotein complex on the regions where the SPP1 replication origins were previously predicted.

摘要

枯草芽孢杆菌噬菌体SPP1 DNA复制的起始需要基因38、39和40的产物(G38P、G39P和G40P)。G38P特异性结合两个离散区域,在SPP1基因组的线性图谱中它们相距32.1 kb。其中一个靶位点位于噬菌体基因组左端的基因38内,已被证明可作为复制起点,因此被称为左起点(oriL)。另一个位点位于基因组右端晚期转录区域的非编码片段内,被称为oriR。这两个位点都包含两种类型的重复元件(称为Box AB和富含A + T的区域)。G38P-oriL DNA和G38P-oriR DNA复合物的K(app)估计分别为1 nM和4 nM。G38P协同结合远处的oriL和oriR位点。DNase I足迹实验表明G38P在Box AB区域有保护作用,但在富含A + T的区域没有。电子显微镜分析表明,G38P通过蛋白质-蛋白质相互作用与SPP1 oriL和oriR位点形成高阶核蛋白结构。G38P在其同源位点的结合似乎不会改变DNA的长度,而是使其弯曲。这些结果表明,G38P在先前预测的SPP1复制起点区域形成核蛋白复合物。

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