Nieto C, Giraldo R, Fernández-Tresguerres E, Díaz R
Centro de Investigaciones Biológicas, C.S.I.C., Madrid, Spain.
J Mol Biol. 1992 Jan 20;223(2):415-26. doi: 10.1016/0022-2836(92)90661-3.
The sequence of a 1823 base-pair region containing the replication functions of pPS10, a narrow host-range plasmid isolated from a strain of Pseudomonas savastanoi, is reported. The origin of replication, oriV, or pPS10 is contained in a 535 base-pair fragment of this sequence that can replicate in the presence of trans-acting function(s) of the plasmid. oriV contains four iterons of 22 base-pairs that are preceded by G+C-rich and A+T-rich regions. A dnaA box located adjacent to the repeats of the origin is dispensable but required for efficient replication of pPS10; A and T are equivalent bases at the 5' end of the box. repA, the gene of a trans-acting replication protein of 26,700 Mr has been identified by genetic and functional analysis. repA is adjacent to the origin of replication and is preceded by the consensus sequences of a typical sigma 70 promoter of Escherichia coli. The RepA protein has been identified, using the minicell system of E. coli, as a polypeptide with an apparent molecular mass of 26,000. A minimal pPS10 replicon has been defined to a continuous 1267 base-pair region of pPS10 that includes the oriV and repA sequences.
报道了来自野油菜黄单胞菌菌株的窄宿主范围质粒pPS10的包含复制功能的1823个碱基对区域的序列。复制起点oriV或pPS10包含在该序列的一个535个碱基对的片段中,该片段在质粒的反式作用功能存在时能够复制。oriV包含四个22个碱基对的迭代子,其前面是富含G+C和富含A+T的区域。位于复制起点重复序列附近的一个dnaA框对于pPS10的有效复制是可有可无但却是必需的;该框5'端的A和T是等效碱基。通过遗传和功能分析鉴定出了repA,它是一个26700道尔顿的反式作用复制蛋白的基因。repA与复制起点相邻,其前面是大肠杆菌典型的sigma 70启动子的共有序列。利用大肠杆菌的微小细胞系统已鉴定出RepA蛋白是一种表观分子量为26000的多肽。已将最小的pPS10复制子定义为pPS10的一个连续的1267个碱基对区域,该区域包括oriV和repA序列。