Wu H, Tyson K L, Cole J A, Busby S J
School of Biochemistry, University of Birmingham, UK.
Mol Microbiol. 1998 Jan;27(2):493-505. doi: 10.1046/j.1365-2958.1998.00699.x.
Expression from the Escherichia coli nir promoter is co-dependent on Fnr (a transcription factor triggered by oxygen starvation) and on NarL or NarP (transcription factors triggered by nitrite and nitrate ions). Fnr binds to a single DNA site centred between basepairs 41 and 42 upstream from the nir transcript start, whereas NarL and NarP bind to a site upstream, centred between basepairs 69 and 70. A novel mechanism to account for co-dependence on Fnr and NarL/NarP is suggested from experiments in which the spacing between the DNA sites for Fnr and NarL/NarP was altered. DNA sequence elements located upstream of the NarL/NarP-binding site are the targets for two or more proteins that act to repress Fnr-dependent activation of the nir promoter. This inhibition is counteracted by NarL or NarP. The model has been corroborated by the effects of several deletions and single base substitutions in the nir promoter upstream sequences: these deletions and substitutions prevent the binding of the repressor proteins. One of these repressors has been identified as the Fis protein, that binds to a site located 135-149bp upstream of the nir transcript start: the binding of Fis is suppressed by a single base substitution at position -146. The other repressor protein(s) have yet to be identified, but appear to bind downstream of the DNA site for Fis: binding is suppressed by a single base substitution at position -99.
大肠杆菌nir启动子的表达共同依赖于Fnr(一种由氧饥饿触发的转录因子)以及NarL或NarP(由亚硝酸盐和硝酸根离子触发的转录因子)。Fnr结合到nir转录本起始位点上游碱基对41和42之间中心位置的单个DNA位点,而NarL和NarP则结合到上游一个位点,该位点位于碱基对69和70之间的中心位置。通过改变Fnr和NarL/NarP的DNA位点之间间距的实验,提出了一种解释对Fnr和NarL/NarP共同依赖的新机制。位于NarL/NarP结合位点上游的DNA序列元件是两种或更多种蛋白质的作用靶点,这些蛋白质会抑制Fnr依赖的nir启动子激活。这种抑制作用会被NarL或NarP抵消。该模型已通过nir启动子上游序列中几个缺失和单碱基替换的效应得到证实:这些缺失和替换会阻止阻遏蛋白的结合。其中一种阻遏蛋白已被鉴定为Fis蛋白,它结合到nir转录本起始位点上游135 - 149bp处的一个位点:在位置 - 146处的单个碱基替换会抑制Fis的结合。其他阻遏蛋白尚未被鉴定,但似乎结合在Fis的DNA位点下游:在位置 - 99处的单个碱基替换会抑制其结合。