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Nucleic Acids Research Advance Access published online on April 25, 2008

Nucleic Acids Research, doi:10.1093/nar/gkn135
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© 2008 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.


Computational Biology

Large-scale computational and statistical analyses of high transcription potentialities in 32 prokaryotic genomes

Christine Sinoquet1,*, Sylvain Demey1 and Frédérique Braun2

1Computer Science Institute of Nantes-Atlantic (Lina), U.M.R. C.N.R.S. 6241, University of Nantes, 2 rue de la Houssinière, BP 92208, 44322 Nantes Cedex and 2Inserm U601, Cancerology Research Department, University of Nantes, 9 quai Moncousu, 44093 Nantes Cedex 01, France

*To whom correspondence should be addressed. Tel: +33(0)25112 5805; Fax: +33(0)25112 5815; Email: christine.sinoquet{at}univ-nantes.fr

Received December 22, 2007. Revised February 20, 2008. Accepted March 10, 2008.

This article compares 32 bacterial genomes with respect to their high transcription potentialities. The {sigma}70 promoter has been widely studied for Escherichia coli model and a consensus is known. Since transcriptional regulations are known to compensate for promoter weakness (i.e. when the promoter similarity with regard to the consensus is rather low), predicting functional promoters is a hard task. Instead, the research work presented here comes within the scope of investigating potentially high ORF expression, in relation with three criteria: (i) high similarity to the {sigma}70 consensus (namely, the consensus variant appropriate for each genome), (ii) transcription strength reinforcement through a supplementary binding site—the upstream promoter (UP) element—and (iii) enhancement through an optimal Shine-Dalgarno (SD) sequence. We show that in the AT-rich Firmicutes genomes, frequencies of potentially strong {sigma}70-like promoters are exceptionally high. Besides, though they contain a low number of strong promoters (SPs), some genomes may show a high proportion of promoters harbouring an UP element. Putative SPs of lesser quality are more frequently associated with an UP element than putative strong promoters of better quality. A meaningful difference is statistically ascertained when comparing bacterial genomes with similarly AT-rich genomes generated at random; the difference is the highest for Firmicutes. Comparing some Firmicutes genomes with similarly AT-rich Proteobacteria genomes, we confirm the Firmicutes specificity. We show that this specificity is neither explained by AT-bias nor genome size bias; neither does it originate in the abundance of optimal SD sequences, a typical and significant feature of Firmicutes more thoroughly analysed in our study.


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