Dole Sudhanshu, Nagarajavel V, Schnetz Karin
Institute for Genetics, University Cologne,Weyertal 121, 50931 Cologne, Germany.
Mol Microbiol. 2004 Apr;52(2):589-600. doi: 10.1111/j.1365-2958.2004.04001.x.
Specificity of repression by the histone-like nucleoid structuring protein and pleiotropic regulator, H-NS, is exceptionally high in case of the Escherichia coli bgl (beta-glucoside) operon. Here we present evidence that H-NS represses the operon at two levels. The binding of H-NS to an upstream silencer results in an approximately threefold repression of the catabolite gene regulator protein (CRP) dependent bgl promoter. In addition, H-NS binds to a silencer region located approximately 600-700 base pairs downstream of the promoter, within the coding region of first gene, bglG, resulting in a approximately sevenfold further decrease of expression. Repression by H-NS at the downstream silencer requires termination factor Rho and is reduced by translation of the bglG mRNA, but is independent of the promoter. This suggests that H-NS induces polarity of transcription by acting as a roadblock to the elongating RNA polymerase. The control of the bgl operon by H-NS at two levels results in a highly specific repression.
在大肠杆菌bgl(β-葡萄糖苷)操纵子的情况下,类组蛋白核仁结构蛋白和多效调节因子H-NS的阻遏特异性极高。在此,我们提供证据表明H-NS在两个水平上阻遏该操纵子。H-NS与上游沉默子的结合导致对依赖于分解代谢基因调节蛋白(CRP)的bgl启动子产生约三倍的阻遏作用。此外,H-NS与位于启动子下游约600 - 700个碱基对处、第一个基因bglG编码区内的一个沉默子区域结合,导致表达进一步降低约七倍。H-NS在下游沉默子处的阻遏作用需要终止因子Rho,并且会因bglG mRNA的翻译而降低,但与启动子无关。这表明H-NS通过作为延伸中的RNA聚合酶的障碍来诱导转录极性。H-NS在两个水平上对bgl操纵子的控制导致了高度特异性的阻遏。