Minchin S D, Austin S, Dixon R A
AFRC-IPSR Nitrogen Fixation Laboratory, University of Sussex, Brighton, UK.
Mol Microbiol. 1988 Jul;2(4):433-42. doi: 10.1111/j.1365-2958.1988.tb00049.x.
The regulatory region spanning the divergently transcribed nifF and nifLA promoters contains a NIFA-specific upstream activator sequence (UAS) located around +59, and two NTRC binding sites centred at -142 and -163 with respect to the nifLA transcription start site. We have constructed mutations in each of these binding sites and examined their role in transcriptional activation of the divergently transcribed promoters. Analysis of a mutation at +60 confirms that the UAS is required for efficient NIFA-mediated activation of nifF transcription. This sequence is also required for maximal activation of the nifLA promoter. Mutations at -169 and -148, within the two NTRC binding sites, reduce activation of the nifLA promoter by NTRC in vivo and lower the affinity of the activator for these sites in vitro. Phosphorylation of NTRC by NTRB is required for efficient binding of NTRC to these sites.
跨越反向转录的nifF和nifLA启动子的调控区域包含一个位于+59左右的NIFA特异性上游激活序列(UAS),以及相对于nifLA转录起始位点分别位于-142和-163中心位置的两个NTRC结合位点。我们在每个这些结合位点构建了突变,并研究了它们在反向转录启动子转录激活中的作用。对+60处突变的分析证实,UAS是NIFA介导的nifF转录有效激活所必需的。该序列也是nifLA启动子最大激活所必需的。两个NTRC结合位点内-169和-148处的突变,在体内降低了NTRC对nifLA启动子的激活作用,并在体外降低了激活剂对这些位点的亲和力。NTRB对NTRC的磷酸化是NTRC有效结合这些位点所必需的。