Gross R, Rappuoli R
Scalvo Research Center, Siena, Italy.
J Bacteriol. 1989 Jul;171(7):4026-30. doi: 10.1128/jb.171.7.4026-4030.1989.
Previous analysis of the pertussis toxin (PT) promoter has shown that expression of PT requires a trans-activating factor encoded by the vir locus and a 170-base-pair DNA sequence upstream from the transcription start site containing a 21-base-pair direct repeat sequence crucial trans-activation (R. Gross and R. Rappuoli, Proc. Natl. Acad. Sci. USA 85:3913-3917, 1988). In this paper we extend the analysis to the modulative response to environmental stimuli. We show that modulation acts at the transcriptional level and occurs only in phase I bacteria. Modulation also requires a functional vir locus and the same promoter region of 170 base pairs. We show that, in addition to the previously identified direct repeat, even the sequences downstream from position -117 are required for trans-activation and modulation and that the deletion of four cytosine residues at position -31 causes the inactivation of the promoter. The kinetics of the change in transcription show that the PT promoter can be shut off very rapidly by adding 50 mM MgSO4 to the medium, whereas resumption of transcription after removal of the modulative agents from the medium is slow.
先前对百日咳毒素(PT)启动子的分析表明,PT的表达需要由vir位点编码的反式激活因子以及转录起始位点上游170个碱基对的DNA序列,该序列包含一个对反式激活至关重要的21个碱基对的直接重复序列(R. 格罗斯和R. 拉普奥利,《美国国家科学院院刊》85:3913 - 3917,1988年)。在本文中,我们将分析扩展至对环境刺激的调节反应。我们表明,调节作用发生在转录水平,且仅在I期细菌中出现。调节还需要一个功能性的vir位点以及相同的170个碱基对的启动子区域。我们表明,除了先前鉴定出的直接重复序列外,转录起始位点上游-117位下游的序列对于反式激活和调节也是必需的,并且在-31位缺失四个胞嘧啶残基会导致启动子失活。转录变化的动力学表明,通过向培养基中添加50 mM MgSO4,PT启动子可以非常迅速地关闭,而从培养基中去除调节因子后转录的恢复则很缓慢。