de la Hoz A B, Ayora S, Sitkiewicz I, Fernández S, Pankiewicz R, Alonso J C, Ceglowski P
Department of Microbial Biotechnology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, 28049 Madrid, Spain.
Proc Natl Acad Sci U S A. 2000 Jan 18;97(2):728-33. doi: 10.1073/pnas.97.2.728.
Transcription initiation of the copy-number control and better-than-random segregation genes of the broad-host-range and low-copy-number plasmid pSM19035 are subjected to repression by the autoregulated pSM19035-encoded omega product in Bacillus subtilis cells. The promoters of the copS (Pcop1 and Pcop2), delta (Pdelta), and omega (Pomega) genes have been mapped. These promoters are embedded in a set of either seven copies of a 7-bp direct repeat or in a block consisting of two 7-bp direct repeats and one 7-bp inverted repeat; the blocks are present either two or three times. The cooperative binding of omega protein to the repeats on the Pcop1, Pcop2, Pdelta, and Pomega promoters represses transcription initiation by a mechanism that does not exclude sigma(A)RNAP from the promoters. These results indicate that omega protein regulates plasmid maintenance by controlling the copy number on the one hand and by regulating the amount of proteins required for better-than-random segregation on the other hand.
在枯草芽孢杆菌细胞中,广宿主范围低拷贝数质粒pSM19035的拷贝数控制基因和优于随机分配基因的转录起始受到pSM19035编码的ω产物自动调控的抑制。已绘制出copS(Pcop1和Pcop2)、δ(Pdelta)和ω(Pomega)基因的启动子图谱。这些启动子嵌入在一组7个碱基对的直接重复序列的7个拷贝中,或者嵌入在由两个7个碱基对的直接重复序列和一个7个碱基对的反向重复序列组成的一个片段中;这些片段存在两次或三次。ω蛋白与Pcop1、Pcop2、Pdelta和Pomega启动子上的重复序列协同结合,通过一种不排除σ(A)RNA聚合酶与启动子结合的机制抑制转录起始。这些结果表明,ω蛋白一方面通过控制拷贝数,另一方面通过调节优于随机分配所需的蛋白量来调节质粒的维持。