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Modulation of inv gene expression by the OmpR two-component response regulator protein of Yersinia enterocolitica
A. Raczkowska, M. Brzóstkowska, A. Kwiatek, J. Bielecki, K. Brzostek
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Adhesins, Bacterial genetics MeSH
- Chromosomes, Bacterial genetics MeSH
- Bacterial Proteins genetics metabolism MeSH
- Escherichia coli genetics metabolism MeSH
- Gene Fusion MeSH
- Transcription, Genetic MeSH
- Lac Operon genetics MeSH
- Osmolar Concentration MeSH
- Promoter Regions, Genetic MeSH
- Gene Expression Regulation, Bacterial MeSH
- Trans-Activators genetics metabolism MeSH
- Yersinia enterocolitica genetics metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
To elucidate the physiological meaning of OmpR-dependent expression of invasin gene (inv) inhibition in Yersinia enterocolitica, the function of the EnvZ/OmpR regulatory pathway in osmoregulation of inv expression was analyzed in detail. The osmoregulation of inv expression was found to be a multifaceted process involving both OmpR-dependent and -independent mechanisms. Analysis of inv transcription in strains lacking OmpR or EnvZ proteins indicated that kinase EnvZ is not the only regulator of OmpR phosphorylation. Using the transcriptional inv::lacZ fusion in a heterologous system (Escherichia coli) we tried to clarify the role of OmpR in the inv regulatory circuit composed of negative (H-NS) and positive (RovA) regulators of inv gene transcription. We were able to show a significant increase in inv expression in E. coli ompR background under H-NS( Ecoli )-repressed condition. Moreover, H-NS-mediated inv repression was relieved when RovA of Y. enterocolitica was expressed from a plasmid. Furthermore, we showed that RovA may activate inv expression irrespective on the presence of H-NS protein. Using this strategy we showed that OmpR of Y. enterocolitica decrease RovA-mediated inv activation.
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- $a Raczkowska, A. $u Department of Applied Microbiology, University of Warsaw, Faculty of Biology, Institute of Microbiology, Miecznikowa 1, Warsaw, Poland
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- $a To elucidate the physiological meaning of OmpR-dependent expression of invasin gene (inv) inhibition in Yersinia enterocolitica, the function of the EnvZ/OmpR regulatory pathway in osmoregulation of inv expression was analyzed in detail. The osmoregulation of inv expression was found to be a multifaceted process involving both OmpR-dependent and -independent mechanisms. Analysis of inv transcription in strains lacking OmpR or EnvZ proteins indicated that kinase EnvZ is not the only regulator of OmpR phosphorylation. Using the transcriptional inv::lacZ fusion in a heterologous system (Escherichia coli) we tried to clarify the role of OmpR in the inv regulatory circuit composed of negative (H-NS) and positive (RovA) regulators of inv gene transcription. We were able to show a significant increase in inv expression in E. coli ompR background under H-NS( Ecoli )-repressed condition. Moreover, H-NS-mediated inv repression was relieved when RovA of Y. enterocolitica was expressed from a plasmid. Furthermore, we showed that RovA may activate inv expression irrespective on the presence of H-NS protein. Using this strategy we showed that OmpR of Y. enterocolitica decrease RovA-mediated inv activation.
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