Research Article: The cross-species prediction of bacterial promoters using a support vector machine

  • Authors:
  • Michael Towsey;Peter Timms;James Hogan;Sarah A. Mathews

  • Affiliations:
  • School of Life Sciences, Faculty of Science, Queensland University of Queensland, GPO Box 2434, Brisbane, Queensland 4001, Australia and School of Software Engineering and Data Communications, Fac ...;School of Life Sciences, Faculty of Science, Queensland University of Queensland, GPO Box 2434, Brisbane, Queensland 4001, Australia and Institute of Health and Biomedical Innovation, Cnr Blamey S ...;School of Software Engineering and Data Communications, Faculty of Information Technology, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia;School of Life Sciences, Faculty of Science, Queensland University of Queensland, GPO Box 2434, Brisbane, Queensland 4001, Australia and Institute of Health and Biomedical Innovation, Cnr Blamey S ...

  • Venue:
  • Computational Biology and Chemistry
  • Year:
  • 2008

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Abstract

Due to degeneracy of the observed binding sites, the in silico prediction of bacterial @s^7^0-like promoters remains a challenging problem. A large number of @s^7^0-like promoters has been biologically identified in only two species, Escherichia coli and Bacillus subtilis. In this paper we investigate the issues that arise when searching for promoters in other species using an ensemble of SVM classifiers trained on E. coli promoters. DNA sequences are represented using a tagged mismatch string kernel. The major benefit of our approach is that it does not require a prior definition of the typical -35 and -10 hexamers. This gives the SVM classifiers the freedom to discover other features relevant to the prediction of promoters. We use our approach to predict @s^A promoters in B. subtilis and @s^6^6 promoters in Chlamydia trachomatis. We extended the analysis to identify specific regulatory features of gene sets in C. trachomatis having different expression profiles. We found a strong -35 hexamer and TGN/-10 associated with a set of early expressed genes. Our analysis highlights the advantage of using TSS-PREDICT as a starting point for predicting promoters in species where few are known.