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 Cabrera, J. E.
Right arrow Articles by Jin, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cabrera, J. E.
Right arrow Articles by Jin, D. J.

 Previous Article  |  Next Article 

Journal of Bacteriology, October 2001, p. 6126-6134, Vol. 183, No. 20
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.20.6126-6134.2001

Growth Phase and Growth Rate Regulation of the rapA Gene, Encoding the RNA Polymerase-Associated Protein RapA in Escherichia coli

Julio E. Cabrera and Ding Jun Jin*

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892

Received 14 May 2001/Accepted 16 July 2001

The Escherichia coli rapA gene encodes the RNA polymerase (RNAP)-associated protein RapA, which is a bacterial member of the SWI/SNF helicase-like protein family. We have studied the rapA promoter and its regulation in vivo and determined the interaction between RNAP and the promoter in vitro. We have found that the expression of rapA is growth phase dependent, peaking at the early log phase. The growth phase control of rapA is determined at least by one particular feature of the promoter: it uses CTP as the transcription-initiating nucleotide instead of a purine, which is used for most E. coli promoters. We also found that the rapA promoter is subject to growth rate regulation in vivo and that it forms intrinsic unstable initiation complexes with RNAP in vitro. Furthermore, we have shown that a GC-rich or discriminator sequence between the -10 and +1 positions of the rapA promoter is responsible for its growth rate control and the instability of its initiation complexes with RNAP.


* Corresponding author. Mailing address: Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Building 37, Room 2B16, 9000 Rockville Pike, Bethesda, MD 20892. Phone: (301) 402-9281. Fax: (301) 594-3611. E-mail: djjin{at}helix.nih.gov.


Journal of Bacteriology, October 2001, p. 6126-6134, Vol. 183, No. 20
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.20.6126-6134.2001



This article has been cited by other articles:

  • Husnain, S. I., Busby, S. J. W., Thomas, M. S. (2009). Downregulation of the Escherichia coli guaB Promoter by Upstream-Bound Cyclic AMP Receptor Protein. J. Bacteriol. 191: 6094-6104 [Abstract] [Full Text]  
  • Lynch, S. V., Dixon, L., Benoit, M. R., Brodie, E. L., Keyhan, M., Hu, P., Ackerley, D. F., Andersen, G. L., Matin, A. (2007). Role of the rapA Gene in Controlling Antibiotic Resistance of Escherichia coli Biofilms. Antimicrob. Agents Chemother. 51: 3650-3658 [Abstract] [Full Text]  
  • Kawano, M., Storz, G., Rao, B. S., Rosner, J. L., Martin, R. G. (2005). Detection of low-level promoter activity within open reading frame sequences of Escherichia coli. Nucleic Acids Res 33: 6268-6276 [Abstract] [Full Text]  
  • Walker, K. A., Mallik, P., Pratt, T. S., Osuna, R. (2004). The Escherichia coli fis Promoter Is Regulated by Changes in the Levels of Its Transcription Initiation Nucleotide CTP. J. Biol. Chem. 279: 50818-50828 [Abstract] [Full Text]  
  • Zhi, H., Wang, X., Cabrera, J. E., Johnson, R. C., Jin, D. J. (2003). Fis Stabilizes the Interaction between RNA Polymerase and the Ribosomal Promoter rrnB P1, Leading to Transcriptional Activation. J. Biol. Chem. 278: 47340-47349 [Abstract] [Full Text]  
  • Voloshin, O. N., Vanevski, F., Khil, P. P., Camerini-Otero, R. D. (2003). Characterization of the DNA Damage-inducible Helicase DinG from Escherichia coli. J. Biol. Chem. 278: 28284-28293 [Abstract] [Full Text]  
  • Sukhodolets, M. V., Cabrera, J. E., Zhi, H., Jin, D. J. (2001). RapA, a bacterial homolog of SWI2/SNF2, stimulates RNA polymerase recycling in transcription. Genes Dev. 15: 3330-3341 [Abstract] [Full Text]