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赖斯氏菌属调控因子AtzR结合位点:参与激活、抑制及氰尿酸依赖性重新定位的DNA序列

The LysR-type regulator AtzR binding site: DNA sequences involved in activation, repression and cyanuric acid-dependent repositioning.

作者信息

Porrúa Odil, García-Jaramillo Manuel, Santero Eduardo, Govantes Fernando

机构信息

Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide/CSIC, and Departamento de Biología Molecular e Ingeniería Bioquímica, Universidad Pablo de Olavide.

出版信息

Mol Microbiol. 2007 Oct;66(2):410-27. doi: 10.1111/j.1365-2958.2007.05927.x. Epub 2007 Sep 14.

DOI:10.1111/j.1365-2958.2007.05927.x
PMID:17854404
Abstract

The LysR-type transcriptional regulator (LTTR) AtzR of Pseudomonas sp. strain ADP activates the cyanuric acid-utilization atzDEF operon in response to low nitrogen availability and the presence of cyanuric acid. AtzR also represses expression of its own gene, atzR, transcribed divergently from atzDEF. Here we identify and functionally characterize the cis-acting sequences at the atzR-atzDEF divergent promoter region required for AtzR-dependent regulation. AtzR binds a single site overlapping both the PatzR and PatzDEF promoters and induces a DNA bend immediately upstream from PatzDEF. Interaction of AtzR with the inducer cyanuric acid shortens the protein-DNA interaction region and relaxes the DNA bend. The AtzR binding site contains a strong binding determinant, the repression binding site (RBS), centred at position -65 relative to the atzDEF transcriptional start, containing the LTTR binding consensus motif. Integrity of the RBS is essential for high-affinity AtzR binding, activation and autorepression. A second, weaker binding determinant, the activation binding site (ABS), is present between the RBS and PatzDEF. Deletion of the ABS only provokes a modest decrease in AtzR affinity for the promoter region in vitro, but abolishes repression of PatzR in vivo. Involvement of the ABS in autorepression has not been previously reported.

摘要

假单胞菌属ADP菌株的LysR型转录调节因子(LTTR)AtzR可响应低氮可用性和氰尿酸的存在激活氰尿酸利用atzDEF操纵子。AtzR还抑制其自身基因atzR的表达,atzR与atzDEF转录方向相反。在此,我们鉴定并功能表征了AtzR依赖性调控所需的atzR-atzDEF反向启动子区域的顺式作用序列。AtzR结合一个与PatzR和PatzDEF启动子均重叠的单一位点,并在PatzDEF上游紧邻处诱导DNA弯曲。AtzR与诱导物氰尿酸的相互作用缩短了蛋白质-DNA相互作用区域并使DNA弯曲松弛。AtzR结合位点包含一个强结合决定簇,即阻遏结合位点(RBS),相对于atzDEF转录起始位点位于-65位置,包含LTTR结合共有基序。RBS的完整性对于高亲和力AtzR结合、激活和自阻遏至关重要。第二个较弱的结合决定簇,即激活结合位点(ABS),存在于RBS和PatzDEF之间。仅缺失ABS在体外仅引起AtzR对启动子区域亲和力的适度降低,但在体内消除了PatzR的阻遏作用。ABS参与自阻遏作用此前尚未见报道。

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