Kelley W, Bastia D
Proc Natl Acad Sci U S A. 1985 May;82(9):2574-8. doi: 10.1073/pnas.82.9.2574.
The replication initiator protein of plasmid R6K preferentially repressed transcription initiated in vitro from the promoter of the initiator protein cistron. DNase I protection experiments revealed that the sequences in the region of the promoter recognized by the initiator protein partially overlapped the sequences of the same promoter recognized by RNA polymerase of Escherichia coli. Competitive DNase I protection experiments revealed that the initiator not only prevented the RNA polymerase from binding to the promoter sequence but also displaced RNA polymerase from preformed enzyme-promoter binary complexes. Thus, the initiator protein acts as a transcriptional repressor of its own cistron by either preventing RNA polymerase from binding to the promoter or by displacing RNA polymerase from promoter-enzyme complexes.
质粒R6K的复制起始蛋白优先抑制从起始蛋白顺反子启动子体外起始的转录。DNA酶I保护实验表明,起始蛋白识别的启动子区域中的序列与大肠杆菌RNA聚合酶识别的同一启动子的序列部分重叠。竞争性DNA酶I保护实验表明,起始蛋白不仅阻止RNA聚合酶与启动子序列结合,还能将RNA聚合酶从预先形成的酶-启动子二元复合物中置换出来。因此,起始蛋白通过阻止RNA聚合酶与启动子结合或从启动子-酶复合物中置换RNA聚合酶,作为其自身顺反子的转录阻遏物。