Browning Douglas F, Cole Jeffrey A, Busby Stephen J W
School of Biosciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
J Bacteriol. 2008 Nov;190(21):7258-67. doi: 10.1128/JB.01015-08. Epub 2008 Aug 29.
The Escherichia coli K-12 nir operon promoter can be fully activated by binding of the regulator of fumarate and nitrate reduction (FNR) to a site centered at position -41.5 upstream of the transcript start, and this activation is modulated by upstream binding of the integration host factor (IHF) and Fis (factor for inversion stimulation) proteins. Thus, transcription initiation is repressed by the binding of IHF and Fis to sites centered at position -88 (IHF I) and position -142 (Fis I) and activated by IHF binding to a site at position -115 (IHF II). Here, we have exploited mutational analysis and biochemistry to investigate the actions of IHF and Fis at these sites. We show that the effects of IHF and Fis are position dependent and that IHF II functions independently of IHF I and Fis I. Using in vitro assays, we report that IHF and Fis repress transcription initiation by interfering with RNA polymerase binding. Differences in the upstream IHF and Fis binding sites at the nir promoter in related enteric bacteria fix the level of nir operon expression under anaerobic growth conditions.
大肠杆菌K-12 nir操纵子启动子可通过延胡索酸和硝酸盐还原调节因子(FNR)与转录起始位点上游-41.5位置中心的位点结合而被完全激活,并且这种激活受整合宿主因子(IHF)和Fis(倒位刺激因子)蛋白的上游结合调节。因此,转录起始受到IHF和Fis与-88位置(IHF I)和-142位置(Fis I)中心位点的结合的抑制,并受到IHF与-115位置(IHF II)位点的结合的激活。在此,我们利用突变分析和生物化学方法来研究IHF和Fis在这些位点的作用。我们表明,IHF和Fis的作用是位置依赖性的,并且IHF II的功能独立于IHF I和Fis I。通过体外试验,我们报告IHF和Fis通过干扰RNA聚合酶结合来抑制转录起始。相关肠道细菌中nir启动子上游IHF和Fis结合位点的差异决定了厌氧生长条件下nir操纵子的表达水平。