Zargar M A, Pandey B, Sharma R, Chakravorty M
Molecular Biology Unit, Banaras Hindu University, Varanasi, U.P., India.
Virus Genes. 1997;14(2):137-46. doi: 10.1023/a:1007969301840.
A strong promoter of bacteriophage MB78 does not have minus 35 consensus sequence although it has a TGn motif immediately upstream of minus 10 sequence as well as the AT rich UP element. It is efficiently recognised by the sigma 70 RNA polymerase, however, a phage-specific factor competes with sigma 70 RNA polymerase for binding to this region, the binding of the factor being stronger than that of the polymerase. Contrary to the reports in the literature the polymerase appears not to bind to the UP element whereas the phage-specific factor does. The latter seems to be involved in the regulation of the promoter activity.
噬菌体MB78的一个强启动子没有-35共有序列,尽管它在-10序列上游紧邻处有一个TGn基序以及富含AT的上游元件(UP元件)。它能被σ70 RNA聚合酶有效识别,然而,一种噬菌体特异性因子与σ70 RNA聚合酶竞争结合该区域,该因子的结合比聚合酶更强。与文献报道相反,聚合酶似乎不结合UP元件,而噬菌体特异性因子能结合。后者似乎参与启动子活性的调控。