Taguchi Y, Tanaka K, Honda Y, Miao D M, Sakai H, Komano T, Bagdasarian M
Laboratory of Biochemistry, Department of Agricultural Chemistry, Kyoto University, Japan.
FEBS Lett. 1996 Jun 17;388(2-3):169-72. doi: 10.1016/0014-5793(96)00558-3.
The initiation of replication from oriV RSF1010, the replication origin of the broad host-range plasmid RSF1010, depends on RepA (helicase), RepB' (primase), and RepC (initiator protein), encoded by RSF1010 itself, while this initiation event in E. coli is independent of dnaA, dnaB, dnaC, and dnaG [Scherzinger et al. (1984) Proc. Natl. Acad. Sci. USA 81, 654-658; Scholz et al. (1985) in: Plasmids in Bacteria, pp. 243-259, Plenum, New York; Haring and Scherzinger (1989) in: Promiscuous Plasmids of Gram-negative Bacteria, pp. 95-124, Academic Press, London; Scherzinger et al. (1991) Nucl. Acids Res. 19, 1203-1211]. We showed in this work that a newly constructed origin consisting of an oriV RSF1010 and a DnaA protein binding site, the dnaA box, inserted near oriV RSF1010 (oriV RSF1010-dnaA box) could function without RepB' primase, but required RepA and RepC. This oriV RsF1010-dnaA box could not replicate in a dnaA46 strain in which only RepA and RepC were supplied, even at a permissive temperature. These results indicate that an inserted dnaA box can functionally substitute for the RSF1010-specific ssi signals, the RepB' dependent priming signals in oriV RSF1010, and can direct a priming pathway different from the RSF1010-specific one, but related to DnaA protein.
来自广宿主范围质粒RSF1010的复制起点oriV RSF1010的复制起始依赖于RSF1010自身编码的RepA(解旋酶)、RepB'(引发酶)和RepC(起始蛋白),而在大肠杆菌中这种起始事件不依赖于dnaA、dnaB、dnaC和dnaG [舍尔青格等人(1984年)《美国国家科学院院刊》81,654 - 658;朔尔茨等人(1985年)载于:《细菌中的质粒》,第243 - 259页,普伦出版社,纽约;哈林和舍尔青格(1989年)载于:《革兰氏阴性菌的滥交质粒》,第95 - 124页,学术出版社,伦敦;舍尔青格等人(1991年)《核酸研究》19,1203 - 1211]。我们在这项工作中表明,一个新构建的由oriV RSF1010和一个插入在oriV RSF1010附近的DnaA蛋白结合位点即dnaA框组成的起点(oriV RSF1010 - dnaA框)可以在没有RepB'引发酶的情况下发挥功能,但需要RepA和RepC。这个oriV RsF1010 - dnaA框即使在允许温度下也不能在仅提供RepA和RepC的dnaA46菌株中复制。这些结果表明,插入的dnaA框可以在功能上替代RSF1010特异性的ssi信号,即oriV RSF1010中依赖RepB'的引发信号,并且可以引导一条不同于RSF1010特异性途径但与DnaA蛋白相关的引发途径。