Unveiling Mycoplasma hyopneumoniae Promoters: Sequence Definition and Genomic Distribution

Several Mycoplasma species have had their genome completely sequenced, including four strains of the swine pathogen Mycoplasma hyopneumoniae. Nevertheless, little is known about the nucleotide sequences that control transcriptional initiation in these microorganisms. Therefore, with the objective of...

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Published in:DNA research Vol. 19; no. 2; pp. 103 - 115
Main Authors: Weber, Shana de Souto, Sant'Anna, Fernando Hayashi, Schrank, Irene Silveira
Format: Journal Article
Language:English
Published: Oxford Oxford University Press 01-04-2012
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Summary:Several Mycoplasma species have had their genome completely sequenced, including four strains of the swine pathogen Mycoplasma hyopneumoniae. Nevertheless, little is known about the nucleotide sequences that control transcriptional initiation in these microorganisms. Therefore, with the objective of investigating the promoter sequences of M. hyopneumoniae, 23 transcriptional start sites (TSSs) of distinct genes were mapped. A pattern that resembles the σ70 promoter –10 element was found upstream of the TSSs. However, no –35 element was distinguished. Instead, an AT-rich periodic signal was identified. About half of the experimentally defined promoters contained the motif 5'-TRTGn-3', which was identical to the –16 element usually found in Gram-positive bacteria. The defined promoters were utilized to build position-specific scoring matrices in order to scan putative promoters upstream of all coding sequences (CDSs) in the M. hyopneumoniae genome. Two hundred and one signals were found associated with 169 CDSs. Most of these sequences were located within 100 nucleotides of the start codons. This study has shown that the number of promoter-like sequences in the M. hyopneumoniae genome is more frequent than expected by chance, indicating that most of the sequences detected are probably biologically functional.
Bibliography:http://dx.doi.org/10.1093/dnares/dsr045
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
Edited by Katsumi Isono
ISSN:1340-2838
1756-1663
DOI:10.1093/dnares/dsr045