Previous Article | Next Article 
Infection and Immunity, January 2001, p. 186-193, Vol. 69, No. 1
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.186-193.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Novel Group of Virulence Activators within the AraC
Family That Are Not Restricted to Upstream Binding Sites
George P.
Munson,
Lisa G.
Holcomb, and
June R.
Scott*
Department of Microbiology and Immunology,
Emory University School of Medicine, Atlanta, Georgia 30322
Received 3 August 2000/Returned for modification 21 September
2000/Accepted 2 October 2000
Several regulators within the AraC family control the expression of
genes known or thought to be required for virulence of bacterial
pathogens. One of these, Rns, activates transcription from an
unprecedented variety of binding-site locations. Although nearly all
prokaryotic activators bind within a small region upstream and adjacent
to the promoter that they regulate, Rns does not bind within this
region to activate its own promoter, Prns. Instead, to
activate Prns, Rns requires one binding site 224.5 bp
upstream and one downstream of the transcription start site. We show in this study that several other AraC family activators recognize the same
binding sites as Rns and share with it the ability to utilize a
downstream binding site. Like Rns, other members of this group of
activators positively regulate the expression of virulence factors in
pathogenic bacteria. These regulators are also able to activate
transcription from promoter-proximal upstream binding sites since they
are able to substitute for Rns at Pcoo, a promoter with
only upstream binding sites. Thus, Rns is the prototype for a group of
regulators, which include CfaR, VirF, AggR, and CsvR and which activate
transcription from locations that are more diverse than those of any
other known activator.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Emory University School of Medicine,
Atlanta, GA 30322. Phone: (404) 727-0402. Fax: (404) 727-8999. E-mail: Scott{at}microbio.emory.edu.
Infection and Immunity, January 2001, p. 186-193, Vol. 69, No. 1
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.186-193.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Basturea, G. N., Bodero, M. D., Moreno, M. E., Munson, G. P.
(2008). Residues near the Amino Terminus of Rns Are Essential for Positive Autoregulation and DNA Binding. J. Bacteriol.
190: 2279-2285
[Abstract]
[Full Text]
-
Mellies, J. L., Barron, A. M. S., Carmona, A. M.
(2007). Enteropathogenic and Enterohemorrhagic Escherichia coli Virulence Gene Regulation. Infect. Immun.
75: 4199-4210
[Full Text]
-
Pilonieta, M. C., Bodero, M. D., Munson, G. P.
(2007). CfaD-Dependent Expression of a Novel Extracytoplasmic Protein from Enterotoxigenic Escherichia coli. J. Bacteriol.
189: 5060-5067
[Abstract]
[Full Text]
-
Bodero, M. D., Pilonieta, M. C., Munson, G. P.
(2007). Repression of the Inner Membrane Lipoprotein NlpA by Rns in Enterotoxigenic Escherichia coli. J. Bacteriol.
189: 1627-1632
[Abstract]
[Full Text]
-
Lyzen, R., Wegrzyn, G., Wegrzyn, A., Szalewska-Palasz, A.
(2006). Stimulation of the {lambda} pR promoter by Escherichia coli SeqA protein requires downstream GATC sequences and involves late stages of transcription initiation.. Microbiology
152: 2985-2992
[Abstract]
[Full Text]
-
Arabolaza, A., Banchio, C., Gramajo, H.
(2006). Transcriptional regulation of the macs1-fadD1 operon encoding two acyl-CoA synthases involved in the physiological differentiation of Streptomyces coelicolor. Microbiology
152: 1427-1439
[Abstract]
[Full Text]
-
Knowle, D., Lintner, R. E., Touma, Y. M., Blumenthal, R. M.
(2005). Nature of the Promoter Activated by C.PvuII, an Unusual Regulatory Protein Conserved among Restriction-Modification Systems. J. Bacteriol.
187: 488-497
[Abstract]
[Full Text]
-
Froehlich, B., Holtzapple, E., Read, T. D., Scott, J. R.
(2004). Horizontal Transfer of CS1 Pilin Genes of Enterotoxigenic Escherichia coli. J. Bacteriol.
186: 3230-3237
[Abstract]
[Full Text]
-
Recchi, C., Sclavi, B., Rauzier, J., Gicquel, B., Reyrat, J.-M.
(2003). Mycobacterium tuberculosis Rv1395 Is a Class III Transcriptional Regulator of the AraC Family Involved in Cytochrome P450 Regulation. J. Biol. Chem.
278: 33763-33773
[Abstract]
[Full Text]
-
Clarke, S. C., Haigh, R. D., Freestone, P. P. E., Williams, P. H.
(2003). Virulence of Enteropathogenic Escherichia coli, a Global Pathogen. Clin. Microbiol. Rev.
16: 365-378
[Abstract]
[Full Text]
-
Ruiz, R., Marques, S., Ramos, J. L.
(2003). Leucines 193 and 194 at the N-Terminal Domain of the XylS Protein, the Positive Transcriptional Regulator of the TOL meta-Cleavage Pathway, Are Involved in Dimerization. J. Bacteriol.
185: 3036-3041
[Abstract]
[Full Text]
-
Ibarra, J. A., Villalba, M. I., Puente, J. L.
(2003). Identification of the DNA Binding Sites of PerA, the Transcriptional Activator of the bfp and per Operons in Enteropathogenic Escherichia coli. J. Bacteriol.
185: 2835-2847
[Abstract]
[Full Text]
-
Egan, S. M.
(2002). Growing Repertoire of AraC/XylS Activators. J. Bacteriol.
184: 5529-5532
[Full Text]
-
Tramonti, A., Visca, P., De Canio, M., Falconi, M., De Biase, D.
(2002). Functional Characterization and Regulation of gadX, a Gene Encoding an AraC/XylS-Like Transcriptional Activator of the Escherichia coli Glutamic Acid Decarboxylase System. J. Bacteriol.
184: 2603-2613
[Abstract]
[Full Text]
-
Munson, G. P., Holcomb, L. G., Alexander, H. L., Scott, J. R.
(2002). In Vitro Identification of Rns-Regulated Genes. J. Bacteriol.
184: 1196-1199
[Abstract]
[Full Text]
-
Porter, M. E., Dorman, C. J.
(2002). In Vivo DNA-Binding and Oligomerization Properties of the Shigella flexneri AraC-Like Transcriptional Regulator VirF as Identified by Random and Site-Specific Mutagenesis. J. Bacteriol.
184: 531-539
[Abstract]
[Full Text]
-
Okeke, I. N., Borneman, J. A., Shin, S., Mellies, J. L., Quinn, L. E., Kaper, J. B.
(2001). Comparative Sequence Analysis of the Plasmid-Encoded Regulator of Enteropathogenic Escherichia coli Strains. Infect. Immun.
69: 5553-5564
[Abstract]
[Full Text]