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一个参与大肠杆菌ompF基因负调控的远上游位点。

A distant upstream site involved in the negative regulation of the Escherichia coli ompF gene.

作者信息

Huang K J, Schieberl J L, Igo M M

机构信息

Section of Microbiology, University of California, Davis 95616.

出版信息

J Bacteriol. 1994 Mar;176(5):1309-15. doi: 10.1128/jb.176.5.1309-1315.1994.

Abstract

The two-component regulatory system, OmpR-EnvZ, of Escherichia coli K-12 regulates the expression of the major outer membrane porin protein, OmpF. OmpR is a DNA-binding protein which acts as both an activator and a repressor to control ompF transcription. In this article, we describe a new OmpR-binding site that is located between 384 to 351 bp upstream from the ompF start point of transcription. Inactivation of this site by insertion of a 22-bp fragment prevents the repression of ompF expression conferred by the dominant negative mutation, envZ473. On the basis of the location of this binding site, the presence of bent DNA in the ompF regulatory region (T. Mizuno, Gene 54:57-64, 1987), and the fact that mutations altering integration host factor result in constitutive ompF expression (P. Tsui, V. Helu, and M. Freundlich, J. Bacteriol. 170:4950-4953, 1988), we propose that the negative regulation of ompF involves a DNA loop structure.

摘要

大肠杆菌K-12的双组分调节系统OmpR-EnvZ调控主要外膜孔蛋白OmpF的表达。OmpR是一种DNA结合蛋白,作为激活剂和阻遏物来控制ompF的转录。在本文中,我们描述了一个新的OmpR结合位点,它位于ompF转录起始点上游384至351 bp之间。通过插入一个22 bp的片段使该位点失活,可阻止显性负突变envZ473对ompF表达的抑制作用。基于该结合位点的位置、ompF调控区域中弯曲DNA的存在(T. Mizuno,《基因》54:57 - 64,1987)以及改变整合宿主因子的突变导致ompF组成型表达这一事实(P. Tsui、V. Helu和M. Freundlich,《细菌学杂志》170:4950 - 4953,1988),我们提出ompF的负调控涉及一种DNA环结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cfe/205194/7358b81fd375/jbacter00023-0117-a.jpg

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