This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
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 Gronewold, T. M. A.
Right arrow Articles by Kaiser, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gronewold, T. M. A.
Right arrow Articles by Kaiser, D.

 Previous Article  |  Next Article 

Journal of Bacteriology, March 2007, p. 1836-1844, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01618-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Mutations of the Act Promoter in Myxococcus xanthus{triangledown} ,{dagger}

Thomas M. A. Gronewold{ddagger} and Dale Kaiser*

Departments of Biochemistry and of Developmental Biology, Stanford University School of Medicine, Stanford, California 94305

Received 17 October 2006/ Accepted 12 December 2006

Mutations within the –12 and –24 elements provide evidence that the act promoter is recognized by sigma-54 RNA polymerase. Deletion of the –20 base pair, which lies between the two conserved elements of sigma-54 promoters, decreased expression by 90%. In addition, mutation of a potential enhancer sequence, around –120, led to an 80% reduction in act gene expression. actB, the second gene in the act operon, encodes a sigma-54 activator protein that is proposed to be an enhancer-binding protein for the act operon. All act genes, actA to actE, are expressed together and constitute an operon, because an in-frame deletion of actB decreased expression of actA and actE to the same extent. After an initially slow phase of act operon expression, which depends on FruA, there is a rapid phase. The rapid phase is shown to be due to the activation of the operon expression by ActB, which completes a positive feedback loop. That loop appears to be nested within a larger positive loop in which ActB is activated by the C signal via ActA, and the act operon activates transcription of the csgA gene. We propose that, as cells engage in more C signaling, positive feedback raises the number of C-signal molecules per cell and drives the process of fruiting body development forward.


* Corresponding author. Mailing address: Department of Developmental Biology, Beckman Center, B300, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305-5329. Phone: (650) 723-6165. Fax: (650) 725-7739. E-mail: kaiser{at}cmgm.stanford.edu.

{triangledown} Published ahead of print on 22 December 2006.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.

{ddagger} Present address: Center of Advanced European Studies and Research, Ludwig-Erhard-Allee 2, 53175 Bonn, Germany.


Journal of Bacteriology, March 2007, p. 1836-1844, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01618-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Ossa, F., Diodati, M. E., Caberoy, N. B., Giglio, K. M., Edmonds, M., Singer, M., Garza, A. G. (2007). The Myxococcus xanthus Nla4 Protein Is Important for Expression of Stringent Response-Associated Genes, ppGpp Accumulation, and Fruiting Body Development. J. Bacteriol. 189: 8474-8483 [Abstract] [Full Text]