Properties of RNA polymerase bypass mutants -: Implications for the role of ppGpp and its co-factor DksA in controlling transcription dependent on σ54
Properties of RNA polymerase bypass mutants -: Implications for the role of ppGpp and its co-factor DksA in controlling transcription dependent on σ54
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DOI：
10.1074/jbc.m610181200
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发表时间：
2007-06-22
影响因子：
4.8
通讯作者：
Shingler, Victoria
中科院分区：
文献类型：
--
作者：
Szalewska-Palasz, Agnieszka;Johansson, Linda U. M.;Shingler, Victoria
The bacterial nutritional and stress alarmone ppGpp and its co-factor DksA directly bind RNA polymerase to regulate its activity at certain sigma(70)-dependent promoters. A number of promoters that are dependent on alternative sigma-factors function poorly in the absence of ppGpp. These include the Pseudomonas-derived sigma(54)-dependent Po promoter and several other sigma(54-)promoters, the transcription from which is essentially abolished in Escherichia coli devoid of ppGpp and DksA. However, ppGpp and DksA have no apparent effect on reconstituted in vitro sigma(54)-transcription, which suggests an indirect mechanism of control. Here we report analysis of five hyper-suppressor mutants within the beta- and beta'-subunits of core RNA polymerase that allow high levels of transcription from the sigma(54)-Po promoter in the absence of ppGpp. Using in vitro transcription and competition assays, we present evidence that these core RNA polymerase mutants are defective in one or both of two properties that could combine to explain their hyper-suppressor phenotypes: (i) modulation of competitive association with sigma-factors to favor sigma(54)-holoenzyme formation over that with sigma(70), and (ii) reduced innate stability of RNA polymerase-promoter complexes, which mimics the essential effects of ppGpp and DksA for negative regulation of stringent sigma(70)-promoters. Both these properties of the mutant holoenzymes support a recently proposed mechanism for regulation of sigma(54)-transcription that depends on the potent negative effects of ppGpp and DksA on transcription from powerful stringent sigma(70)-promoters, and suggests that stringent regulation is a key mechanism by which the activity of alternative sigma-factors is controlled to meet cellular requirements.
