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大肠杆菌stpA基因在丰富培养基中生长期间短暂表达,并在基本培养基中以及在应激条件下被诱导表达。

The Escherichia coli stpA gene is transiently expressed during growth in rich medium and is induced in minimal medium and by stress conditions.

作者信息

Free A, Dorman C J

机构信息

Department of Microbiology, Trinity College, Dublin 2, Republic of Ireland.

出版信息

J Bacteriol. 1997 Feb;179(3):909-18. doi: 10.1128/jb.179.3.909-918.1997.

Abstract

The transcriptional regulation of the stpA gene, encoding the Escherichia coli H-NS-like protein StpA, has been studied as a function of a variety of environmental conditions, and its response to trans-acting factors has been characterized. Chromosomally located stpA is expressed primarily from a promoter immediately upstream of the gene which is severely repressed by the homologous nucleoid-associated protein H-NS. However, we show here that even in a strain containing functional H-NS, stpA is transiently induced during growth of a batch culture in rich medium. It can also be induced strongly by osmotic shock and, to a lesser extent, by an increase in growth temperature. Moreover, when cells are grown in minimal medium, we observe a more sustained induction of stpA which is dependent on the leucine-responsive regulatory protein (Lrp). This enhanced level of stpA transcription is virtually abolished in an H-NS-independent manner when the culture undergoes carbon starvation. A sensitivity of the stpA promoter to DNA topology may contribute to some of these responses. Results reported here show that cloned fragments of the stpA promoter region can confer H-NS and Lrp responsiveness upon a lacZ reporter gene and suggest that several hundred base pairs of DNA upstream of the transcriptional start may be required for regulation by these two proteins.

摘要

编码大肠杆菌H-NS样蛋白StpA的stpA基因的转录调控已作为多种环境条件的函数进行了研究,并且其对反式作用因子的反应也已得到表征。位于染色体上的stpA主要从该基因上游紧邻的一个启动子表达,该启动子受到同源类核相关蛋白H-NS的严重抑制。然而,我们在此表明,即使在含有功能性H-NS的菌株中,stpA在丰富培养基中分批培养生长期间也会被短暂诱导。它也可被渗透压休克强烈诱导,在较小程度上还可被生长温度升高诱导。此外,当细胞在基本培养基中生长时,我们观察到stpA有更持续的诱导,这依赖于亮氨酸响应调节蛋白(Lrp)。当培养物经历碳饥饿时,这种增强的stpA转录水平以不依赖H-NS的方式几乎完全消失。stpA启动子对DNA拓扑结构的敏感性可能是这些反应的部分原因。此处报道的结果表明,stpA启动子区域的克隆片段可赋予lacZ报告基因对H-NS和Lrp的响应性,并表明转录起始上游几百个碱基对的DNA可能是这两种蛋白进行调控所必需的。

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