Timmis K N, Andrés I, Achtman M
Proc Natl Acad Sci U S A. 1978 Dec;75(12):5836-40. doi: 10.1073/pnas.75.12.5836.
The locations of the fertility inhibition genes finO and finP of the F-like conjugative multiple antibiotic-resistance plasmid R6-5 have been determined. As found previously for that of the fertility plasmid F, the finP gene of R6-5 is located close to the origin of DNA transfer, oriT, and to the promoter-proximal segment of the tra operon. Thus, finP is close to the site of action of the FinOP fertility inhibition system. In contrast, the finO gene is located on the other side of the tra operon, greater than 35 kilobases from the finP gene; finO is very close to the origin of vegetative replication, oriV, and to cistrons encoding functions involved in autonomous plasmid replication and plasmid incompatibility. A 4.5-kilobase fragment of R6-5 DNA containing the finO gene has been cloned on the high-copy amplifiable vector plasmid pBR322. This hybrid plasmid, designated pKTO31, causes severe repression of conjugal transfer of plasmid F, indicating the production of high cellular levels of finO protein. Two independent finO mutant derivatives were obtained after mutagenesis of the pKTO31 plasmid. Comparison of proteins synthesized by minicells carrying finO(-) mutant plasmids with those carrying various finO(+) plasmids enables the finO gene product to be tentatively identified as a 22,000-dalton protein.
已确定F类接合型多重抗生素抗性质粒R6 - 5的育性抑制基因finO和finP的位置。正如先前对育性质粒F的研究发现,R6 - 5的finP基因位于DNA转移起点oriT附近,以及tra操纵子的启动子近端区域。因此,finP靠近FinOP育性抑制系统的作用位点。相比之下,finO基因位于tra操纵子的另一侧,距离finP基因超过35千碱基;finO非常靠近营养复制起点oriV,以及编码参与自主质粒复制和质粒不相容性功能的顺反子。含有finO基因的R6 - 5 DNA的一个4.5千碱基片段已克隆到高拷贝可扩增载体质粒pBR322上。这个杂种质粒,命名为pKTO31,导致质粒F的接合转移受到严重抑制,表明细胞内产生了高水平的finO蛋白。在对pKTO31质粒进行诱变后获得了两个独立的finO突变衍生物。通过比较携带finO(-)突变体质粒的微小细胞与携带各种finO(+)质粒的微小细胞合成的蛋白质,初步确定finO基因产物为一种22000道尔顿的蛋白质。