Literature DB >> 12675812

DNA supercoiling contributes to disconnect sigmaS accumulation from sigmaS-dependent transcription in Escherichia coli.

Patricia Bordes1, Annie Conter, Violette Morales, Jean Bouvier, Annie Kolb, Claude Gutierrez.   

Abstract

The sigmaS subunit of RNA polymerase is a key regulator of Escherichia coli transcription in stress conditions. sigmaS accumulates in cells subjected to stresses such as an osmotic upshift or the entry into stationary phase. We show here that, at elevated osmolarity, sigmaS accumulates long before the beginning of the sigmaS-dependent induction of osmEp, one of its target promoters. A combination of in vivo and in vitro evidence indicates that a high level of DNA negative supercoiling inhibits transcription by EsigmaS. The variations in superhelical densities occurring as a function of growth conditions can modulate transcription of a subset of sigmaS targets and thereby contribute to the temporal disconnection between the accumulation of sigmaS and sigmaS-driven transcription. We propose that, in stress conditions leading to the accumulation of sigmaS without lowering the growth rate, the level of DNA supercoiling acts as a checkpoint that delays the shift from the major (Esigma70) to the general stress (EsigmaS) transcriptional machinery, retarding the induction of a subset of the sigmaS regulon until the conditions become unfavourable enough to cause entry into stationary phase.

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Year:  2003        PMID: 12675812     DOI: 10.1046/j.1365-2958.2003.03461.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  30 in total

1.  Interactions between the 2.4 and 4.2 regions of sigmaS, the stress-specific sigma factor of Escherichia coli, and the -10 and -35 promoter elements.

Authors:  Claire Checroun; Patricia Bordes; Olivier Leroy; Annie Kolb; Claude Gutierrez
Journal:  Nucleic Acids Res       Date:  2004-01-02       Impact factor: 16.971

2.  Gene order and chromosome dynamics coordinate spatiotemporal gene expression during the bacterial growth cycle.

Authors:  Patrick Sobetzko; Andrew Travers; Georgi Muskhelishvili
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-19       Impact factor: 11.205

Review 3.  Integration of syntactic and semantic properties of the DNA code reveals chromosomes as thermodynamic machines converting energy into information.

Authors:  Georgi Muskhelishvili; Andrew Travers
Journal:  Cell Mol Life Sci       Date:  2013-06-15       Impact factor: 9.261

Review 4.  DNA supercoiling is a fundamental regulatory principle in the control of bacterial gene expression.

Authors:  Charles J Dorman; Matthew J Dorman
Journal:  Biophys Rev       Date:  2016-06-16

Review 5.  The regulatory role of DNA supercoiling in nucleoprotein complex assembly and genetic activity.

Authors:  Georgi Muskhelishvili; Andrew Travers
Journal:  Biophys Rev       Date:  2016-11-19

Review 6.  DNA supercoiling is a fundamental regulatory principle in the control of bacterial gene expression.

Authors:  Charles J Dorman; Matthew J Dorman
Journal:  Biophys Rev       Date:  2016-11-14

Review 7.  Genome architecture and global gene regulation in bacteria: making progress towards a unified model?

Authors:  Charles J Dorman
Journal:  Nat Rev Microbiol       Date:  2013-04-03       Impact factor: 60.633

8.  Analysis of the ospC regulatory element controlled by the RpoN-RpoS regulatory pathway in Borrelia burgdorferi.

Authors:  Xiaofeng F Yang; Meghan C Lybecker; Utpal Pal; Sophie M Alani; Jon Blevins; Andrew T Revel; D Scott Samuels; Michael V Norgard
Journal:  J Bacteriol       Date:  2005-07       Impact factor: 3.490

9.  Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulation.

Authors:  Pooja Rawal; Veera Bhadra Rao Kummarasetti; Jinoy Ravindran; Nirmal Kumar; Kangkan Halder; Rakesh Sharma; Mitali Mukerji; Swapan Kumar Das; Shantanu Chowdhury
Journal:  Genome Res       Date:  2006-05       Impact factor: 9.043

10.  Loss of topoisomerase I function affects the RpoS-dependent and GAD systems of acid resistance in Escherichia coli.

Authors:  Natalee Stewart; Jingyang Feng; Xiaoping Liu; Devyani Chaudhuri; John W Foster; Marc Drolet; Yuk-Ching Tse-Dinh
Journal:  Microbiology (Reading)       Date:  2005-08       Impact factor: 2.777

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