| Literature DB >> 27237053 |
Wilma Ross1, Patricia Sanchez-Vazquez1, Albert Y Chen1, Jeong-Hyun Lee1, Hector L Burgos1, Richard L Gourse2.
Abstract
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.Entities:
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Year: 2016 PMID: 27237053 PMCID: PMC4912440 DOI: 10.1016/j.molcel.2016.04.029
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970