Ross Wilma, Sanchez-Vazquez Patricia, Chen Albert Y, Lee Jeong-Hyun, Burgos Hector L, Gourse Richard L
Department of Bacteriology, University of Wisconsin-Madison, 1550 Linden Drive, Madison, WI 53706, USA.
Department of Bacteriology, University of Wisconsin-Madison, 1550 Linden Drive, Madison, WI 53706, USA.
Mol Cell. 2016 Jun 16;62(6):811-823. doi: 10.1016/j.molcel.2016.04.029. Epub 2016 May 26.
Throughout the bacterial domain, the alarmone ppGpp dramatically reprograms transcription following nutrient limitation. This "stringent response" is critical for survival and antibiotic tolerance and is a model for transcriptional regulation by small ligands. We report that ppGpp binds to two distinct sites 60 Å apart on E. coli RNA polymerase (RNAP), one characterized previously (site 1) and a second identified here at an interface of RNAP and the transcription factor DksA (site 2). The location and unusual tripartite nature of site 2 account for the DksA-ppGpp synergism and suggest mechanisms for ppGpp enhancement of DksA's effects on RNAP. Site 2 binding results in the majority of ppGpp's effects on transcription initiation in vitro and in vivo, and strains lacking site 2 are severely impaired for growth following nutritional shifts. Filling of the two sites at different ppGpp concentrations would expand the dynamic range of cellular responses to changes in ppGpp levels.
在整个细菌域中,警报素鸟苷四磷酸(ppGpp)在营养限制后会显著重新编程转录。这种“严格反应”对于生存和抗生素耐受性至关重要,并且是小分子配体进行转录调控的一个模型。我们报告称,ppGpp结合在大肠杆菌RNA聚合酶(RNAP)上相距60埃的两个不同位点,一个是先前已确定的(位点1),另一个是在此处确定的位于RNAP与转录因子DksA的界面处(位点2)。位点2的位置和不寻常的三重性质解释了DksA-ppGpp的协同作用,并提出了ppGpp增强DksA对RNAP作用的机制。位点2的结合导致了ppGpp在体外和体内对转录起始的大部分影响,并且缺乏位点2的菌株在营养变化后生长严重受损。在不同的ppGpp浓度下填充这两个位点将扩大细胞对ppGpp水平变化反应的动态范围。