This Article
Right arrow Full Text
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 Glover, R. T.
Right arrow Articles by Jacobs, W. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Glover, R. T.
Right arrow Articles by Jacobs, W. R., Jr.

 Previous Article  |  Next Article 

Journal of Bacteriology, August 2007, p. 5495-5503, Vol. 189, No. 15
0021-9193/07/$08.00+0     doi:10.1128/JB.00190-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

The Two-Component Regulatory System senX3-regX3 Regulates Phosphate-Dependent Gene Expression in Mycobacterium smegmatis{triangledown}

Robert T. Glover,1,2 Jordan Kriakov,1,2 Scott J. Garforth,2 Anthony D. Baughn,1,2 and William R. Jacobs Jr.1,2*

Howard Hughes Medical Institute,1 Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York 104612

Received 5 February 2007/ Accepted 15 May 2007

Phosphate import is required for the growth of mycobacteria and is regulated by environmental inorganic phosphate (Pi) concentrations, although the mechanism of this regulation has not been characterized. The expression of genes involved in Pi acquisition is frequently regulated by two-component regulatory systems (2CRs) consisting of a sensor histidine kinase and a DNA-binding response regulator. In this work, we have identified the senX3-regX3 2CR as a Pi-dependent regulator of genes involved in phosphate acquisition in Mycobacterium smegmatis. Characterization of senX3 mutants with different PhoA phenotypes suggests a dual role for SenX3 as a phosphatase or a phosphodonor for the response regulator RegX3, depending upon Pi availability. Expression of PhoA activity required phosphorylation of RegX3, consistent with a role for phosphorylated RegX3 (RegX3~P) as a transcriptional activator of phoA. Furthermore, purified RegX3~P bound to promoter sequences from phoA, senX3, and the high-affinity phosphate transporter component pstS, demonstrating direct transcriptional control of all three genes. DNase I footprinting and primer extension analyses have further defined the DNA-binding region and transcriptional start site within the phoA promoter. A DNA motif consisting of an inverted repeat was identified in each of the promoters bound by RegX3~P. Based upon our findings, we propose a model for Pi-regulated gene expression mediated by SenX3-RegX3 in mycobacteria.


* Corresponding author. Mailing address: Albert Einstein College of Medicine, Department of Microbiology and Immunology, 1300 Morris Park Avenue, Forchheimer 405, Bronx, NY 10461. Phone: (718) 430-2888. Fax: (718) 518-0366. E-mail: jacobs{at}aecom.yu.edu

{triangledown} Published ahead of print on 25 May 2007.


Journal of Bacteriology, August 2007, p. 5495-5503, Vol. 189, No. 15
0021-9193/07/$08.00+0     doi:10.1128/JB.00190-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Gupta, S., Pathak, A., Sinha, A., Sarkar, D. (2009). Mycobacterium tuberculosis PhoP Recognizes Two Adjacent Direct-Repeat Sequences To Form Head-to-Head Dimers. J. Bacteriol. 191: 7466-7476 [Abstract] [Full Text]  
  • Garcia Pelayo, M. C., Uplekar, S., Keniry, A., Mendoza Lopez, P., Garnier, T., Nunez Garcia, J., Boschiroli, L., Zhou, X., Parkhill, J., Smith, N., Hewinson, R. G., Cole, S. T., Gordon, S. V. (2009). A Comprehensive Survey of Single Nucleotide Polymorphisms (SNPs) across Mycobacterium bovis Strains and M. bovis BCG Vaccine Strains Refines the Genealogy and Defines a Minimal Set of SNPs That Separate Virulent M. bovis Strains and M. bovis BCG Strains. Infect. Immun. 77: 2230-2238 [Abstract] [Full Text]  
  • Chacon, O., Bermudez, L. E., Zinniel, D. K., Chahal, H. K., Fenton, R. J., Feng, Z., Hanford, K., Adams, L. G., Barletta, R. G. (2009). Impairment of D-alanine biosynthesis in Mycobacterium smegmatis determines decreased intracellular survival in human macrophages. Microbiology 155: 1440-1450 [Abstract] [Full Text]  
  • Gebhard, S., Cook, G. M. (2008). Differential Regulation of High-Affinity Phosphate Transport Systems of Mycobacterium smegmatis: Identification of PhnF, a Repressor of the phnDCE Operon. J. Bacteriol. 190: 1335-1343 [Abstract] [Full Text]  
  • King-Scott, J., Nowak, E., Mylonas, E., Panjikar, S., Roessle, M., Svergun, D. I., Tucker, P. A. (2007). The Structure of a Full-length Response Regulator from Mycobacterium tuberculosis in a Stabilized Three-dimensional Domain-swapped, Activated State. J. Biol. Chem. 282: 37717-37729 [Abstract] [Full Text]