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百日咳博德特氏菌中百日咳杆菌粘附素基因启动子的BvgA激活分析。

Analysis of BvgA activation of the pertactin gene promoter in Bordetella pertussis.

作者信息

Kinnear S M, Boucher P E, Stibitz S, Carbonetti N H

机构信息

Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.

出版信息

J Bacteriol. 1999 Sep;181(17):5234-41. doi: 10.1128/JB.181.17.5234-5241.1999.

Abstract

Bordetella pertussis, the causative agent of whooping cough, regulates expression of its virulence factors via a two-component signal transduction system encoded by the bvg regulatory locus. It has been shown by activation kinetics that several of the virulence factors are differentially regulated. fha is transcribed at 10 min following an inducing signal, while ptx is not transcribed until 2 to 4 h after the inducing signal. We present data indicating that prn is transcribed at 1 h, an intermediate time compared to those of fha and ptx. We have identified cis-acting sequences necessary for expression of prn in B. pertussis by using prn-lac fusions containing alterations in the sequence upstream of the prn open reading frame. In vitro transcription and DNase I footprinting analyses provided evidence to support our hypothesis that BvgA binds to this sequence upstream of prn to activate transcription from the promoter. Our genetic data indicate that the region critical for prn activation extends upstream to position -84. However, these data do not support the location of the prn transcription start site as previously published. We used a number of methods, including prn-lac fusions, reverse transcriptase PCR, and 5' rapid amplification of cDNA ends, to localize and identify the bvg-dependent 5' end of the prn transcript to the cytosine at -125 with respect to the published start site.

摘要

百日咳博德特氏菌是百日咳的病原体,它通过由bvg调控位点编码的双组分信号转导系统来调节其毒力因子的表达。通过激活动力学研究表明,几种毒力因子受到不同的调控。fha在诱导信号发出后10分钟开始转录,而ptx直到诱导信号发出后2至4小时才开始转录。我们提供的数据表明,prn在1小时时转录,这一时间介于fha和ptx之间。我们通过使用在prn开放阅读框上游序列中含有改变的prn-lac融合体,鉴定出了百日咳博德特氏菌中prn表达所必需的顺式作用序列。体外转录和DNase I足迹分析提供了证据来支持我们的假设,即BvgA结合到prn上游的该序列上以激活启动子的转录。我们的遗传学数据表明,对prn激活至关重要的区域向上游延伸至-84位。然而,这些数据并不支持先前发表的prn转录起始位点的位置。我们使用了多种方法,包括prn-lac融合体、逆转录酶PCR和5' cDNA末端快速扩增,将prn转录本的bvg依赖性5'末端相对于已发表的起始位点定位并鉴定为-125位的胞嘧啶。

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