DksA and ppGpp Regulate the σ S Stress Response by Activating Promoters for the Small RNA DsrA and the Anti-Adapter Protein IraP.

Autor: Girard ME; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA., Gopalkrishnan S; Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA., Grace ED; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA., Halliday JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Gourse RL; Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA., Herman C; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA herman@bcm.edu.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Jazyk: angličtina
Zdroj: Journal of bacteriology [J Bacteriol] 2017 Dec 20; Vol. 200 (2). Date of Electronic Publication: 2017 Dec 20 (Print Publication: 2018).
DOI: 10.1128/JB.00463-17
Abstrakt: σ S is an alternative sigma factor, encoded by the rpoS gene, that redirects cellular transcription to a large family of genes in response to stressful environmental signals. This so-called σ S general stress response is necessary for survival in many bacterial species and is controlled by a complex, multifactorial pathway that regulates σ S levels transcriptionally, translationally, and posttranslationally in Escherichia coli It was shown previously that the transcription factor DksA and its cofactor, ppGpp, are among the many factors governing σ S synthesis, thus playing an important role in activation of the σ S stress response. However, the mechanisms responsible for the effects of DksA and ppGpp have not been elucidated fully. We describe here how DksA and ppGpp directly activate the promoters for the anti-adaptor protein IraP and the small regulatory RNA DsrA, thereby indirectly influencing σ S levels. In addition, based on effects of DksA N88I , a previously identified DksA variant with increased affinity for RNA polymerase (RNAP), we show that DksA can increase σ S activity by another indirect mechanism. We propose that by reducing rRNA transcription, DksA and ppGpp increase the availability of core RNAP for binding to σ S and also increase transcription from other promoters, including P dsrA and P iraP By improving the translation and stabilization of σ S , as well as the ability of other promoters to compete for RNAP, DksA and ppGpp contribute to the switch in the transcription program needed for stress adaptation. IMPORTANCE Bacteria spend relatively little time in log phase outside the optimized environment found in a laboratory. They have evolved to make the most of alternating feast and famine conditions by seamlessly transitioning between rapid growth and stationary phase, a lower metabolic mode that is crucial for long-term survival. One of the key regulators of the switch in gene expression that characterizes stationary phase is the alternative sigma factor σ S Understanding the factors governing σ S activity is central to unraveling the complexities of growth, adaptation to stress, and pathogenesis. Here, we describe three mechanisms by which the RNA polymerase binding factor DksA and the second messenger ppGpp regulate σ S levels.
(Copyright © 2017 American Society for Microbiology.)
Databáze: MEDLINE
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