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Nucleic Acids Research, 2001, Vol. 29, No. 12 2607-2618
© 2001 Oxford University Press

GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions

John Besemer1, Alexandre Lomsadze1,3 and Mark Borodovsky1,2,*

1School of Biology and 2School of Mathematics, Georgia Institute of Technology, Atlanta, GA 30332-0230, USA and 3Gene Probe, Inc., 883 Heritage Place, Atlanta, GA 30033-4103, USA

Improving the accuracy of prediction of gene starts is one of a few remaining open problems in computer prediction of prokaryotic genes. Its difficulty is caused by the absence of relatively strong sequence patterns identifying true translation initiation sites. In the current paper we show that the accuracy of gene start prediction can be improved by combining models of protein-coding and non-coding regions and models of regulatory sites near gene start within an iterative Hidden Markov model based algorithm. The new gene prediction method, called GeneMarkS, utilizes a non-supervised training procedure and can be used for a newly sequenced prokaryotic genome with no prior knowledge of any protein or rRNA genes. The GeneMarkS implementation uses an improved version of the gene finding program GeneMark.hmm, heuristic Markov models of coding and non-coding regions and the Gibbs sampling multiple alignment program. GeneMarkS predicted precisely 83.2% of the translation starts of GenBank annotated Bacillus subtilis genes and 94.4% of translation starts in an experimentally validated set of Escherichia coli genes. We have also observed that GeneMarkS detects prokaryotic genes, in terms of identifying open reading frames containing real genes, with an accuracy matching the level of the best currently used gene detection methods. Accurate translation start prediction, in addition to the refinement of protein sequence N-terminal data, provides the benefit of precise positioning of the sequence region situated upstream to a gene start. Therefore, sequence motifs related to transcription and translation regulatory sites can be revealed and analyzed with higher precision. These motifs were shown to possess a significant variability, the functional and evolutionary connections of which are discussed.

* To whom correspondence should be addressed at: School of Biology, Georgia Institute of Technology, Atlanta, GA 30332-0230, USA. Tel: +1 404 894 8432; Fax: +1 404 894 0519; Email: mark{at}amber.gatech.edu


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