Wing H J, Williams S M, Busby S J
School of Biochemistry, University of Birmingham, United Kingdom.
J Bacteriol. 1995 Dec;177(23):6704-10. doi: 10.1128/jb.177.23.6704-6710.1995.
We cloned a consensus DNA site for the Escherichia coli FNR protein at different locations upstream of the E. coli melR promoter. FNR can activate transcription initiation at the melR promoter when the FNR binding site is centered around 41, 61, 71, 82, and 92 bp upstream from the transcription start. The SF73 positive control amino acid substitution in FNR interfered with transcription activation by FNR in each case. In contrast, the GA85 positive control substitution reduced activation only at the promoter, where the FNR binding site is 41 bp upstream of the transcript start. The SF73 substitution appears to identify an activating region of FNR that is important for transcription activation at promoters that differ in architecture. Experiments with oriented heterodimers showed that this activating region is functional in the upstream subunit of the FNR dimer at the promoter where FNR binds around 41 bp from the transcript start and in the downstream subunit at the promoters where FNR binds farther upstream.
我们在大肠杆菌melR启动子上游的不同位置克隆了大肠杆菌FNR蛋白的共有DNA位点。当FNR结合位点位于转录起始点上游约41、61、71、82和92 bp处时,FNR可激活melR启动子处的转录起始。在每种情况下,FNR中的SF73阳性对照氨基酸取代都会干扰FNR的转录激活。相比之下,GA85阳性对照取代仅在FNR结合位点位于转录起始点上游41 bp的启动子处降低激活作用。SF73取代似乎确定了FNR的一个激活区域,该区域对于结构不同的启动子处的转录激活很重要。对定向异二聚体的实验表明,该激活区域在FNR结合位点距转录起始点约41 bp的启动子处FNR二聚体的上游亚基中起作用,而在FNR结合更上游的启动子处的下游亚基中也起作用。