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分析盐诱导上调 CagA 表达所需的幽门螺杆菌 cagA 启动子元件。

Analysis of Helicobacter pylori cagA promoter elements required for salt-induced upregulation of CagA expression.

机构信息

Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

出版信息

Infect Immun. 2012 Sep;80(9):3094-106. doi: 10.1128/IAI.00232-12. Epub 2012 Jun 18.

Abstract

Helicobacter pylori infection and consumption of a high-salt diet are each associated with an increased risk for the development of gastric cancer. To investigate potential synergism between these factors, we used a global proteomic approach to analyze H. pylori strains cultured in media containing varying salt concentrations. Among the differentially expressed proteins identified, CagA exhibited the greatest increase in expression in response to high salt concentrations. Analysis of 36 H. pylori strains isolated from patients in two regions of Colombia with differing incidences of gastric cancer revealed marked differences among strains in salt-responsive CagA expression. Sequence analysis of the cagA promoter region in these strains revealed a DNA motif (TAATGA) that was present in either one or two copies. Salt-induced upregulation of CagA expression was detected more commonly in strains containing two copies of the TAATGA motif than in strains containing one copy. Mutagenesis experiments confirmed that two copies of the TAATGA motif are required for salt-induced upregulation of CagA expression. In summary, there is considerable heterogeneity among H. pylori strains in salt-regulated CagA expression, and these differences are attributable to variation in a specific DNA motif upstream of the cagA transcriptional start site.

摘要

幽门螺杆菌感染和高盐饮食均会增加胃癌发生的风险。为了研究这些因素之间的潜在协同作用,我们使用了一种全局蛋白质组学方法来分析在含有不同盐浓度的培养基中培养的幽门螺杆菌菌株。在鉴定出的差异表达蛋白中,CagA 蛋白在高盐浓度下的表达增加最为显著。对来自哥伦比亚两个胃癌发病率不同地区的 36 株幽门螺杆菌的分析表明,盐响应性 CagA 表达在菌株间存在显著差异。对这些菌株中 cagA 启动子区域的序列分析显示,存在一个或两个 TAATGA 基序。含有两个 TAATGA 基序的菌株中更常检测到盐诱导的 CagA 表达上调,而含有一个 TAATGA 基序的菌株则不然。突变实验证实,盐诱导 CagA 表达上调需要两个 TAATGA 基序。总之,在盐调节的 CagA 表达方面,幽门螺杆菌菌株之间存在相当大的异质性,这些差异归因于 cagA 转录起始位点上游特定 DNA 基序的变异。

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