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dc.contributor.authorSchuster, Martinen_US
dc.contributor.authorGreenberg, E. Peteren_US
dc.date.accessioned2010-04-21T15:52:28Z
dc.date.available2010-04-21T15:52:28Z
dc.date.issued2007en_US
dc.identifier.citationSchuster M, Greenberg EP. Early activation of quorum sensing in Pseudomonas aeruginosa reveals the architecture of a complex regulon. BMC Genomics. 2007;8(1):287.en_US
dc.identifier.other10.1186/1471-2164-8-287en_US
dc.identifier.urihttp://www.biomedcentral.com/1471-2164/8/287en_US
dc.identifier.urihttp://hdl.handle.net/1773/15746
dc.description.abstractBackground: Quorum-sensing regulation of gene expression in Pseudomonas aeruginosa is complex. Two interconnected acyl-homoserine lactone (acyl-HSL) signal-receptor pairs, 3-oxododecanoyl-HSL-LasR and butanoyl-HSL-RhlR, regulate more than 300 genes. The induction of most of the genes is delayed during growth of P. aeruginosa in complex medium, cannot be advanced by addition of exogenous signal, and requires additional regulatory components. Many of these late genes can be induced by addition of signals early by using specific media conditions. While several factors super-regulate the quorum receptors, others may co-regulate target promoters or may affect expression posttranscriptionally. Results: To better understand the contributions of super-regulation and co-regulation to quorumsensing gene expression, and to better understand the general structure of the quorum sensing network, we ectopically expressed the two receptors (in the presence of their cognate signals) and another component that affects quorum sensing, the stationary phase sigma factor RpoS, early in growth. We determined the effect on target gene expression by microarray and real-time PCR analysis. Our results show that many target genes (e.g. lasB and hcnABC) are directly responsive to receptor protein levels. Most genes (e.g. lasA, lecA, and phnAB), however, are not significantly affected, although at least some of these genes are directly regulated by quorum sensing. The majority of promoters advanced by RhlR appeared to be regulated directly, which allowed us to build a RhlR consensus sequence. Conclusion: The direct responsiveness of many quorum sensing target genes to receptor protein levels early in growth confirms the role of super-regulation in quorum sensing gene expression. The observation that the induction of most target genes is not affected by signal or receptor protein levels indicates that either target promoters are co-regulated by other transcription factors, or that expression is controlled posttranscriptionally. This architecture permits the integration of multiple signaling pathways resulting in quorum responses that require a "quorum" but are otherwise highly adaptable and receptive to environmental conditions.en_US
dc.description.sponsorshipUSPHS grant GM-59026.en_US
dc.language.isoen_USen_US
dc.titleEarly activation of quorum sensing in Pseudomonas aeruginosa reveals the architecture of a complex regulonen_US
dc.typeArticleen_US


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