Kolter R, Inuzuka M, Helinski D R
Cell. 1978 Dec;15(4):1199-208. doi: 10.1016/0092-8674(78)90046-6.
A non-self-replicating segment (1370 base pairs) of plasmid R6K was cloned in E. coli and shown to trans-complement temperature-sensitive replication mutants of this plasmid. This segment contains the gene which codes for a protein required for initiation of replication of the plasmid, and was used as a helper in a functional assay for an origin of replication in R6K derivatives. A 420 bp fragment, derived from R6K DNA, was shown to carry a functional origin since it was capable of replicating as a plasmid in E. coli cells carrying the helper segment either on the host chromosome or on a plasmid Col E1 derivative. The copy number of the origin fragment in cells carrying the helper segment on the chromosome is essentially the same as the copy number of R6K. A model for the positive regulation of plasmid R6K replication is presented.
质粒R6K的一个非自我复制片段(1370个碱基对)在大肠杆菌中克隆,并被证明能反式互补该质粒的温度敏感型复制突变体。该片段包含编码质粒复制起始所需蛋白质的基因,并在R6K衍生物复制起点的功能检测中用作辅助物。一个源自R6K DNA的420 bp片段被证明携带一个功能性起点,因为它能够在宿主染色体上或质粒Col E1衍生物上携带辅助片段的大肠杆菌细胞中作为质粒进行复制。在染色体上携带辅助片段的细胞中,起点片段的拷贝数与R6K的拷贝数基本相同。本文提出了质粒R6K复制的正调控模型。