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Nucleic Acids Research Advance Access originally published online on November 2, 2007
Nucleic Acids Research 2008 36(1):10-20; doi:10.1093/nar/gkm915
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Nucleic Acids Research, 2008, Vol. 36, No. 1 10-20
© 2007 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

RNA

RNA secondary structure regulates the translation of sxy and competence development in Haemophilus influenzae

Andrew D.S. Cameron1,2, Milica Volar2, Laura A. Bannister2 and Rosemary J. Redfield2,*

1Department of Microbiology and Immunology and 2Department of Zoology, University of British Columbia, Vancouver, British Columbia, Canada

*To whom correspondence should be addressed. Tel: +604 822 3744; Fax: +604 827 4135; Email: redfield{at}zoology.ubc.ca

Received August 24, 2007. Revised October 4, 2007. Accepted October 7, 2007.

The sxy (tfoX) gene product is the central regulator of DNA uptake by naturally competent {gamma}-proteobacteria such as Haemophilus influenzae, Vibrio cholerae and probably Escherichia coli. However, the mechanisms regulating sxy gene expression are not understood despite being key to understanding the physiological role of DNA uptake. We have isolated mutations in H. influenzae sxy that greatly elevate translation and thus cause competence to develop in otherwise non-inducing conditions (hypercompetence). In vitro nuclease analysis confirmed the existence of an extensive secondary structure at the 5' end of sxy mRNA that sequesters the ribosome-binding site and start codon in a stem-loop. All of the hypercompetence mutations reduced mRNA base pairing, and one was shown to cause a global destabilization that increased translational efficiency. Conversely, mutations engineered to add mRNA base pairs strengthened the secondary structure, resulting in reduced translational efficiency and greatly reduced competence for genetic transformation. Transfer of wild-type cells to starvation medium improved translational efficiency of sxy while independently triggering the sugar starvation regulator (CRP) to stimulate transcription at the sxy promoter. Thus, mRNA secondary structure is responsive to conditions where DNA uptake will be favorable, and transcription of sxy is simultaneously enhanced if CRP activation signals that energy supplies are limited.


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 J. Bacteriol.Home page
S. Sinha, A. D. S. Cameron, and R. J. Redfield
Sxy Induces a CRP-S Regulon in Escherichia coli
J. Bacteriol., August 15, 2009; 191(16): 5180 - 5195.
[Abstract] [Full Text] [PDF]


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