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肺炎克雷伯菌nifJ启动子:调控NifA启动子激活的启动子元件分析

The Klebsiella pneumoniae nifJ promoter: analysis of promoter elements regulating activation by the NifA promoter.

作者信息

Charlton W, Cannon W, Buck M

机构信息

AFRC Nitrogen Fixation Laboratory, University of Sussex, Falmer, Brighton, UK.

出版信息

Mol Microbiol. 1993 Mar;7(6):1007-21. doi: 10.1111/j.1365-2958.1993.tb01192.x.

Abstract

The nifJ and nifH promoters of Klebsiella pneumoniae are divergently transcribed sigma 54-dependent promoters that are positively activated by the NifA protein. NifA binds to upstream activator sequences (UASs), usually located 60-200 bp upstream of the start of transcription. Bound NifA is presented to the RNA polymerase-sigma 54 complex (E sigma 54) via DNA loop formation, mediated by the binding of integration host factor protein (IHF) between E sigma 54 and NifA. The nifJ promoter sequence contains three potential NifA binding sites (UAS1, 2 and 3) and two potential RNA polymerase-sigma 54-binding sites (downstream promoter elements, DPEs 1 and 2). DPE2 is located 420 bp into the coding region and DPE1 overlaps UAS1 by 5 bp. Mutational and footprinting analyses have shown efficient activation of the nifJ promoter requires that NifA is bound at UAS 2 and 3. Transcription is initiated at DPE1. Only a weak interaction of NifA with the UAS overlapping DPE1 was detected. Footprints demonstrated that E sigma 54 forms a closed complex at DPE1 but not DPE2 and that bound E sigma 54 closely approaches the -15 region of DPE1. Stimulation of nifJ promoter activity by IHF was not as great as that observed for other nif promoters. In the absence of IHF nifH promoter sequences stimulated activation of the nifJ promoter. This appeared to require NifA bound at the nifH UAS. Thus, one additional role of IHF may be to partition NifA between the two promoters by constraining the topology of the DNA.

摘要

肺炎克雷伯菌的nifJ和nifH启动子是双向转录的依赖σ54的启动子,由NifA蛋白正向激活。NifA与上游激活序列(UASs)结合,UASs通常位于转录起始点上游60 - 200 bp处。通过整合宿主因子蛋白(IHF)在Eσ54和NifA之间的结合介导的DNA环形成,将结合的NifA呈递给RNA聚合酶 - σ54复合物(Eσ54)。nifJ启动子序列包含三个潜在的NifA结合位点(UAS1、2和3)和两个潜在的RNA聚合酶 - σ54结合位点(下游启动子元件,DPEs 1和2)。DPE2位于编码区420 bp处,DPE1与UAS1重叠5 bp。突变和足迹分析表明,nifJ启动子的有效激活要求NifA结合在UAS 2和3处。转录在DPE1处起始。仅检测到NifA与重叠DPE1的UAS有微弱相互作用。足迹显示Eσ54在DPE1处形成封闭复合物,但在DPE2处不形成,并且结合的Eσ54紧密靠近DPE1的 - 15区域。IHF对nifJ启动子活性的刺激不如其他nif启动子观察到的那么大。在没有IHF的情况下,nifH启动子序列刺激了nifJ启动子的激活。这似乎需要NifA结合在nifH UAS处。因此,IHF的另一个作用可能是通过限制DNA的拓扑结构在两个启动子之间分配NifA。

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