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Suppression of FNR-dependent transcription activation at the Escherichia coli nir promoter by Fis, IHF and H-NS: modulation of transcription initiation by a complex nucleo-protein assembly

机译:Fis,IHF和H-NS在大肠杆菌nir启动子上抑制FNR依赖性转录激活:通过复杂的核蛋白组装调节转录起始

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Expression from the Escherichia coil nir promoter is co-dependent on both the FNR protein (an anaerobically triggered transcription activator) and the NarL or Harp proteins (transcription activators triggered by nitrite and nitrate). Under anaerobic conditions, FNR binds to a site centred between positions -41 and -42, activating transcription of the nir operon. In previous work, we showed that this activation is suppressed by the binding of Fis protein, and at least one other protein, to sequence elements located upstream of the nir promoter. We proposed that the binding of NarL or Harp to a site centred between positions -69 and -70 counteracts this suppression, resulting in increased transcription in response to nitrite or nitrate. Here we have further investigated the different proteins that downregulate the nir promoter. We show that the nir promoter is repressed by three DNA binding proteins, Fis, IHF and H-NS. We demonstrate that, in addition to binding to its previously characterized upstream site located at position -142, Fis also binds to a second downstream site located at position +23. A second suppressing factor is IHF, that binds to a site located at position -88. Finally, the nucleoid associated protein, H-NS, preferentially binds to upstream sequences at the nir promoter and represses promoter activity. The association of Fis, IHF and H-NS suggests that nir promoter DNA is sequestrated into a highly ordered nucleo-protein structure that represses FNR-dependent transcription activation. NarL and NarP can relieve both IHF- and Fis-mediated repression, but are unable to counteract H-NS-mediated repression. [References: 44]
机译:大肠杆菌线圈nir启动子的表达共同依赖于FNR蛋白(厌氧触发的转录激活因子)和NarL或Harp蛋白(由亚硝酸盐和硝酸盐触发的转录激活因子)。在厌氧条件下,FNR结合到位于位置-41和-42之间的位点,激活nir操纵子的转录。在以前的工作中,我们表明,Fis蛋白和至少一种其他蛋白与位于nir启动子上游的序列元件的结合可抑制这种激活。我们提出,NarL或Harp结合到位于位置-69和-70之间的位点可以抵消这种抑制,从而导致响应亚硝酸盐或硝酸盐的转录增加。在这里,我们进一步研究了下调nir启动子的不同蛋白质。我们显示,nir启动子被三种DNA结合蛋白,Fis,IHF和H-NS抑制。我们证明,除了与其先前定位在位置-142的上游位点结合外,Fis还与定位在+23位置的第二下游位点结合。第二抑制因子是IHF,其与位于-88位置的位点结合。最后,与核苷相关的蛋白H-NS在nir启动子上优先结合上游序列,并抑制启动子活性。 Fis,IHF和H-NS的关联表明,nir启动子DNA被隔离为抑制FNR依赖性转录激活的高度有序的核蛋白结构。 NarL和NarP可以缓解IHF和Fis介导的阻抑,但不能抵消H-NS介导的阻抑。 [参考:44]

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