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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.
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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.
Published ahead of print on 22 December 2006.
Supplemental material for this article may be found at http://jb.asm.org/.
Present address: Center of Advanced European Studies and Research, Ludwig-Erhard-Allee 2, 53175 Bonn, Germany.
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