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类组蛋白核仁结构蛋白H-NS在启动子下游抑制大肠杆菌bgl操纵子。

The histone-like nucleoid structuring protein H-NS represses the Escherichia coli bgl operon downstream of the promoter.

作者信息

Dole Sudhanshu, Nagarajavel V, Schnetz Karin

机构信息

Institute for Genetics, University Cologne,Weyertal 121, 50931 Cologne, Germany.

出版信息

Mol Microbiol. 2004 Apr;52(2):589-600. doi: 10.1111/j.1365-2958.2004.04001.x.

Abstract

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.

摘要

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。

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