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质粒ColE2-P9复制起点的剖析

Anatomy of the replication origin of plasmid ColE2-P9.

作者信息

Yagura Masaru, Nishio Shin-Ya, Kurozumi Hideki, Wang Cheng-Fu, 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. 2006 Feb;188(3):999-1010. doi: 10.1128/JB.188.3.999-1010.2006.

Abstract

The plasmid ColE2-P9 origin is a 32-bp region which is specifically recognized by the plasmid-specified Rep protein to initiate DNA replication. We analyzed the structural and functional organization of the ColE2 origin by using various derivatives carrying deletions and single-base-pair substitutions. The origin may be divided into three subregions: subregion I, which is important for stable binding of the Rep protein; subregion II, which is important for binding of the Rep protein and for initiation of DNA replication; and subregion III, which is important for DNA replication but apparently not for binding of the Rep protein. The Rep protein might recognize three specific DNA elements in subregions I and II. The relative transformation frequency of the autonomously replicating plasmids carrying deletions in subregion I is lower, and nevertheless the copy numbers of these plasmids in host bacteria are higher than those of the wild-type plasmid. Efficient and stable binding of the Rep protein to the origin might be important for the replication efficiency to be at the normal (low) level. Subregion II might be essential for interaction with the catalytic domain of the Rep protein for primer RNA synthesis. The 8-bp sequence across the border of subregions II and III, including the primer sequence, is conserved in the (putative) origins of many plasmids, the putative Rep proteins of which are related to the ColE2-P9 Rep protein. Subregion III might be required for a step that is necessary after Rep protein binding has taken place.

摘要

质粒ColE2-P9的复制起点是一个32个碱基对的区域,可被质粒特异性的Rep蛋白特异性识别以启动DNA复制。我们通过使用携带缺失和单碱基对替换的各种衍生物分析了ColE2复制起点的结构和功能组织。该复制起点可分为三个子区域:子区域I,对Rep蛋白的稳定结合很重要;子区域II,对Rep蛋白的结合和DNA复制的起始很重要;子区域III,对DNA复制很重要,但显然对Rep蛋白的结合不重要。Rep蛋白可能识别子区域I和II中的三个特定DNA元件。在子区域I中携带缺失的自主复制质粒的相对转化频率较低,然而这些质粒在宿主细菌中的拷贝数高于野生型质粒。Rep蛋白与复制起点的有效和稳定结合可能对复制效率处于正常(低)水平很重要。子区域II可能对于与Rep蛋白的催化结构域相互作用以合成引物RNA至关重要。跨越子区域II和III边界的8个碱基对序列,包括引物序列,在许多质粒的(推定)复制起点中是保守的,其推定的Rep蛋白与ColE2-P9 Rep蛋白相关。子区域III可能是Rep蛋白结合后所需步骤所必需的。

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