This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by De Las Penas, A.
Right arrow Articles by Gross, C. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by De Las Penas, A.
Right arrow Articles by Gross, C. A.

 Previous Article  |  Next Article 

J. Bacteriol., Nov 1997, 6862-6864, Vol 179, No. 21
Copyright © 1997, American Society for Microbiology

SigmaE is an essential sigma factor in Escherichia coli

A De Las Penas, L Connolly and CA Gross
Department of Bacteriology, University of Wisconsin-Madison, 53706, USA.

SigmaE is an alternative sigma factor that controls the extracytoplasmic stress response in Escherichia coli. SigmaE is essential at high temperatures but was previously thought to be nonessential at temperatures below 37 degrees C. We present evidence that sigmaE is an essential sigma factor at all temperatures. Cells lacking sigmaE are able to grow at low temperatures because of the presence of a frequently arising, unlinked suppressor mutation.


This article has been cited by other articles:

  • Mutalik, V. K., Nonaka, G., Ades, S. E., Rhodius, V. A., Gross, C. A. (2009). Promoter Strength Properties of the Complete Sigma E Regulon of Escherichia coli and Salmonella enterica. J. Bacteriol. 191: 7279-7287 [Abstract] [Full Text]  
  • Davis, B. M., Waldor, M. K. (2009). High-throughput sequencing reveals suppressors of Vibrio cholerae rpoE mutations: one fewer porin is enough. Nucleic Acids Res 37: 5757-5767 [Abstract] [Full Text]  
  • Martinez-Salazar, J. M., Salazar, E., Encarnacion, S., Ramirez-Romero, M. A., Rivera, J. (2009). Role of the Extracytoplasmic Function Sigma Factor RpoE4 in Oxidative and Osmotic Stress Responses in Rhizobium etli. J. Bacteriol. 191: 4122-4132 [Abstract] [Full Text]  
  • Noor, R., Murata, M., Nagamitsu, H., Klein, G., Raina, S., Yamada, M. (2009). Dissection of {sigma}E-dependent cell lysis in Escherichia coli: roles of RpoE regulators RseA, RseB and periplasmic folding catalyst PpiD. GENES CELLS 14: 885-899 [Abstract] [Full Text]  
  • Ahuja, N., Korkin, D., Chaba, R., Cezairliyan, B. O., Sauer, R. T., Kim, K. K., Gross, C. A. (2009). Analyzing the Interaction of RseA and RseB, the Two Negative Regulators of the {sigma}E Envelope Stress Response, Using a Combined Bioinformatic and Experimental Strategy. J. Biol. Chem. 284: 5403-5413 [Abstract] [Full Text]  
  • Asai, K., Ishiwata, K., Matsuzaki, K., Sadaie, Y. (2008). A Viable Bacillus subtilis Strain without Functional Extracytoplasmic Function Sigma Genes. J. Bacteriol. 190: 2633-2636 [Abstract] [Full Text]  
  • Flannagan, R. S., Valvano, M. A. (2008). Burkholderia cenocepacia requires RpoE for growth under stress conditions and delay of phagolysosomal fusion in macrophages. Microbiology 154: 643-653 [Abstract] [Full Text]  
  • King-Lyons, N. D., Smith, K. F., Connell, T. D. (2007). Expression of hurP, a Gene Encoding a Prospective Site 2 Protease, Is Essential for Heme-Dependent Induction of bhuR in Bordetella bronchiseptica. J. Bacteriol. 189: 6266-6275 [Abstract] [Full Text]  
  • Carlsson, K. E., Liu, J., Edqvist, P. J., Francis, M. S. (2007). Extracytoplasmic-Stress-Responsive Pathways Modulate Type III Secretion in Yersinia pseudotuberculosis. Infect. Immun. 75: 3913-3924 [Abstract] [Full Text]  
  • Sauviac, L., Philippe, H., Phok, K., Bruand, C. (2007). An Extracytoplasmic Function Sigma Factor Acts as a General Stress Response Regulator in Sinorhizobium meliloti. J. Bacteriol. 189: 4204-4216 [Abstract] [Full Text]  
  • Button, J. E., Silhavy, T. J., Ruiz, N. (2007). A Suppressor of Cell Death Caused by the Loss of {sigma}E Downregulates Extracytoplasmic Stress Responses and Outer Membrane Vesicle Production in Escherichia coli. J. Bacteriol. 189: 1523-1530 [Abstract] [Full Text]  
  • da Silva Neto, J. F., Koide, T., Gomes, S. L., Marques, M. V. (2007). The Single Extracytoplasmic-Function Sigma Factor of Xylella fastidiosa Is Involved in the Heat Shock Response and Presents an Unusual Regulatory Mechanism. J. Bacteriol. 189: 551-560 [Abstract] [Full Text]  
  • Asai, K., Ootsuji, T., Obata, K., Matsumoto, T., Fujita, Y., Sadaie, Y. (2007). Regulatory role of RsgI in sigI expression in Bacillus subtilis. Microbiology 153: 92-101 [Abstract] [Full Text]  
  • Hasenbein, S., Merdanovic, M., Ehrmann, M. (2007). Determinants of regulated proteolysis in signal transduction. Genes Dev. 21: 6-10 [Full Text]  
  • Chaba, R., Grigorova, I. L., Flynn, J. M., Baker, T. A., Gross, C. A. (2007). Design principles of the proteolytic cascade governing the {sigma}E-mediated envelope stress response in Escherichia coli: keys to graded, buffered, and rapid signal transduction. Genes Dev. 21: 124-136 [Abstract] [Full Text]  
  • Guillier, M., Gottesman, S., Storz, G. (2006). Modulating the outer membrane with small RNAs. Genes Dev. 20: 2338-2348 [Abstract] [Full Text]  
  • Costanzo, A., Ades, S. E. (2006). Growth Phase-Dependent Regulation of the Extracytoplasmic Stress Factor, {sigma}E, by Guanosine 3',5'-Bispyrophosphate (ppGpp). J. Bacteriol. 188: 4627-4634 [Abstract] [Full Text]  
  • Douchin, V., Bohn, C., Bouloc, P. (2006). Down-regulation of Porins by a Small RNA Bypasses the Essentiality of the Regulated Intramembrane Proteolysis Protease RseP in Escherichia coli. J. Biol. Chem. 281: 12253-12259 [Abstract] [Full Text]  
  • Wood, L. F., Ohman, D. E. (2006). Independent Regulation of MucD, an HtrA-Like Protease in Pseudomonas aeruginosa, and the Role of Its Proteolytic Motif in Alginate Gene Regulation.. J. Bacteriol. 188: 3134-3137 [Abstract] [Full Text]  
  • Kabir, Md. S., Yamashita, D., Koyama, S., Oshima, T., Kurokawa, K., Maeda, M., Tsunedomi, R., Murata, M., Wada, C., Mori, H., Yamada, M. (2005). Cell lysis directed by {sigma}E in early stationary phase and effect of induction of the rpoE gene on global gene expression in Escherichia coli. Microbiology 151: 2721-2735 [Abstract] [Full Text]  
  • Egler, M., Grosse, C., Grass, G., Nies, D. H. (2005). Role of the Extracytoplasmic Function Protein Family Sigma Factor RpoE in Metal Resistance of Escherichia coli. J. Bacteriol. 187: 2297-2307 [Abstract] [Full Text]  
  • Rowley, G., Stevenson, A., Kormanec, J., Roberts, M. (2005). Effect of Inactivation of degS on Salmonella enterica Serovar Typhimurium In Vitro and In Vivo. Infect. Immun. 73: 459-463 [Abstract] [Full Text]  
  • Grigorova, I. L., Chaba, R., Zhong, H. J., Alba, B. M., Rhodius, V., Herman, C., Gross, C. A. (2004). Fine-tuning of the Escherichia coli {sigma}E envelope stress response relies on multiple mechanisms to inhibit signal-independent proteolysis of the transmembrane anti-sigma factor, RseA. Genes Dev. 18: 2686-2697 [Abstract] [Full Text]  
  • Flynn, J. M., Levchenko, I., Sauer, R. T., Baker, T. A. (2004). Modulating substrate choice: the SspB adaptor delivers a regulator of the extracytoplasmic-stress response to the AAA+ protease ClpXP for degradation. Genes Dev. 18: 2292-2301 [Abstract] [Full Text]  
  • Maxson, M. E., Darwin, A. J. (2004). Identification of Inducers of the Yersinia enterocolitica Phage Shock Protein System and Comparison to the Regulation of the RpoE and Cpx Extracytoplasmic Stress Responses. J. Bacteriol. 186: 4199-4208 [Abstract] [Full Text]  
  • Mooney, R. A., Landick, R. (2003). Tethering {sigma}70 to RNA polymerase reveals high in vivo activity of {sigma} factors and {sigma}70-dependent pausing at promoter-distal locations. Genes Dev. 17: 2839-2851 [Abstract] [Full Text]  
  • Redford, P., Roesch, P. L., Welch, R. A. (2003). degS Is Necessary for Virulence and Is among Extraintestinal Escherichia coli Genes Induced in Murine Peritonitis. Infect. Immun. 71: 3088-3096 [Abstract] [Full Text]  
  • Kinghorn, S. M., O'Byrne, C. P., Booth, I. R., Stansfield, I. (2002). Physiological analysis of the role of truB in Escherichia coli: a role for tRNA modification in extreme temperature resistance. Microbiology 148: 3511-3520 [Abstract] [Full Text]  
  • Kanehara, K., Ito, K., Akiyama, Y. (2002). YaeL (EcfE) activates the sigma E pathway of stress response through a site-2 cleavage of anti-sigma E, RseA. Genes Dev. 16: 2147-2155 [Abstract] [Full Text]  
  • Alba, B. M., Leeds, J. A., Onufryk, C., Lu, C. Z., Gross, C. A. (2002). DegS and YaeL participate sequentially in the cleavage of RseA to activate the sigma E-dependent extracytoplasmic stress response. Genes Dev. 16: 2156-2168 [Abstract] [Full Text]  
  • Craig, J. E., Nobbs, A., High, N. J. (2002). The Extracytoplasmic Sigma Factor, {varsigma}E, Is Required for Intracellular Survival of Nontypeable Haemophilus influenzae in J774 Macrophages. Infect. Immun. 70: 708-715 [Abstract] [Full Text]  
  • Kenyon, W. J., Sayers, D. G., Humphreys, S., Roberts, M., Spector, M. P. (2002). The starvation-stress response of Salmonella enterica serovar Typhimurium requires {sigma}E-, but not CpxR-regulated extracytoplasmic functions. Microbiology 148: 113-122 [Abstract] [Full Text]  
  • Langen, G. R., Harper, J. R., Silhavy, T. J., Howard, S. P. (2001). Absence of the Outer Membrane Phospholipase A Suppresses the Temperature-Sensitive Phenotype of Escherichia coli degP Mutants and Induces the Cpx and {sigma}E Extracytoplasmic Stress Responses. J. Bacteriol. 183: 5230-5238 [Abstract] [Full Text]  
  • Guigueno, A., Dassa, J., Belin, P., Boquet, P. L. (2001). Oversynthesis of a New Escherichia coli Small RNA Suppresses Export Toxicity of DsbA'-PhoA Unfoldable Periplasmic Proteins. J. Bacteriol. 183: 1147-1158 [Abstract] [Full Text]  
  • Hild, E., Takayama, K., Olsson, R.-M., Kjelleberg, S. (2000). Evidence for a Role of rpoE in Stressed and Unstressed Cells of Marine Vibrio angustum Strain S14. J. Bacteriol. 182: 6964-6974 [Abstract] [Full Text]  
  • Collinet, B., Yuzawa, H., Chen, T., Herrera, C., Missiakas, D. (2000). RseB Binding to the Periplasmic Domain of RseA Modulates the RseA:sigma E Interaction in the Cytoplasm and the Availability of sigma E{middle dot}RNA Polymerase. J. Biol. Chem. 275: 33898-33904 [Abstract] [Full Text]  
  • Resto-Ruiz, S. I., Sweger, D., Widen, R. H., Valkov, N., Anderson, B. E. (2000). Transcriptional Activation of the htrA (High-Temperature Requirement A) Gene from Bartonella henselae. Infect. Immun. 68: 5970-5978 [Abstract] [Full Text]  
  • Nitta, T., Nagamitsu, H., Murata, M., Izu, H., Yamada, M. (2000). Function of the sigma E Regulon in Dead-Cell Lysis in Stationary-Phase Escherichia coli. J. Bacteriol. 182: 5231-5237 [Abstract] [Full Text]  
  • Ades, S. E., Connolly, L. E., Alba, B. M., Gross, C. A. (1999). The Escherichia coli sigma E-dependent extracytoplasmic stress response is controlled by the regulated proteolysis of an anti-sigma factor. Genes Dev. 13: 2449-2461 [Abstract] [Full Text]  
  • Cosma, C. L., Crotwell, M. D., Burrows, S. Y., Silhavy, T. J. (1998). . J. Bacteriol. 180: 3120-3130 [Abstract] [Full Text]  
  • Dartigalongue, C., Missiakas, D., Raina, S. (2001). Characterization of the Escherichia colisigma E Regulon. J. Biol. Chem. 276: 20866-20875 [Abstract] [Full Text]