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质粒ColE2-P9和ColE3-CA38复制起始中两个特异性决定因素的不同功能。

Distinct functions of the two specificity determinants in replication initiation of plasmids ColE2-P9 and ColE3-CA38.

作者信息

Aoki Kazuteru, Shinohara Miki, Itoh Tateo

机构信息

Department of Biology, Faculty of Science, Shinshu University, Matsumoto, Nagano 390-8621, Japan.

出版信息

J Bacteriol. 2007 Mar;189(6):2392-400. doi: 10.1128/JB.01695-06. Epub 2007 Jan 19.

Abstract

The plasmid ColE2-P9 Rep protein specifically binds to the cognate replication origin to initiate DNA replication. The replicons of the plasmids ColE2-P9 and ColE3-CA38 are closely related, although the actions of the Rep proteins on the origins are specific to the plasmids. The previous chimera analysis identified two regions, regions A and B, in the Rep proteins and two sites, alpha and beta, in the origins as specificity determinants and showed that when each component of the region A-site alpha pair and the region B-site beta pair is derived from the same plasmid, plasmid DNA replication is efficient. It is also indicated that the replication specificity is mainly determined by region A and site alpha. By using an electrophoretic mobility shift assay, we demonstrated that region B and site beta play a critical role for stable Rep protein-origin binding and, furthermore, that 284-Thr in this region of the ColE2 Rep protein and the corresponding 293-Trp of the ColE3 Rep protein mainly determine the Rep-origin binding specificity. On the other hand, region A and site alpha were involved in the efficient unwinding of several nucleotide residues around site alpha, although they were not involved in the stable binding of the Rep protein to the origin. Finally, we discussed how the action of the Rep protein on the origin involving these specificity determinants leads to the plasmid-specific replication initiation.

摘要

质粒ColE2-P9 Rep蛋白特异性结合同源复制起点以启动DNA复制。质粒ColE2-P9和ColE3-CA38的复制子密切相关,尽管Rep蛋白对复制起点的作用具有质粒特异性。先前的嵌合体分析在Rep蛋白中鉴定出两个区域,即区域A和区域B,在复制起点中鉴定出两个位点,即α位点和β位点,作为特异性决定因素,并表明当区域A-α位点对和区域B-β位点对的每个组分都来自同一质粒时,质粒DNA复制是有效的。还表明复制特异性主要由区域A和α位点决定。通过使用电泳迁移率变动分析,我们证明区域B和β位点对于稳定的Rep蛋白-复制起点结合起关键作用,此外,ColE2 Rep蛋白该区域中的284-苏氨酸和ColE3 Rep蛋白相应的293-色氨酸主要决定Rep-复制起点结合特异性。另一方面,区域A和α位点参与α位点周围几个核苷酸残基的有效解旋,尽管它们不参与Rep蛋白与复制起点的稳定结合。最后,我们讨论了Rep蛋白对涉及这些特异性决定因素的复制起点的作用如何导致质粒特异性复制起始。

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本文引用的文献

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The Rep protein binding elements of the plasmid ColE2-P9 replication origin.质粒ColE2-P9复制起点的Rep蛋白结合元件。
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J Bacteriol. 2006 Feb;188(3):999-1010. doi: 10.1128/JB.188.3.999-1010.2006.
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Mol Cell. 2001 Nov;8(5):937-46. doi: 10.1016/s1097-2765(01)00392-6.
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Plasmid. 2001 Mar;45(2):88-100. doi: 10.1006/plas.2000.1511.
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