Bahk J D, Sakai H, Komano T
Department of Agricultural Chemistry, Kyoto University, Japan.
Gene. 1988 May 15;65(1):93-9. doi: 10.1016/0378-1119(88)90420-9.
Using the plaque assay system for screening the single-strand (ss) initiation determinant (ssi) sequences, we have found that 119-bp region in pACYC184, a derivative of the plasmid P15A of Escherichia coli, can direct such ss DNA initiation. This region is located downstream from the P15A origin of replication and conserves consensus sequences of the ssi signals found in the other plasmids. Signals for ss DNA initiation are defined as nucleotide sequences present on ss DNA templates and required for priming DNA synthesis. The direction of chain elongation in DNA synthesis is opposite to that of the leading strand. In this region, we found a potential stem-and-loop structure. The 119-bp DNA segment of plasmid pACYC184 cloned in f1R199 filamentous phage could direct rifampicin-resistant conversion of the ss DNA to the double-stranded replicative form.
利用噬菌斑检测系统筛选单链(ss)起始决定簇(ssi)序列,我们发现大肠杆菌质粒P15A的衍生物pACYC184中的119 bp区域可指导此类单链DNA起始。该区域位于P15A复制起点的下游,并保留了在其他质粒中发现的ssi信号的共有序列。单链DNA起始信号被定义为单链DNA模板上存在的、启动DNA合成所需的核苷酸序列。DNA合成中的链延伸方向与前导链相反。在该区域,我们发现了一个潜在的茎环结构。克隆到f1R199丝状噬菌体中的质粒pACYC184的119 bp DNA片段可指导单链DNA向双链复制形式的利福平抗性转化。