Modulation of inv gene expression by the OmpR two-component response regulator protein of Yersinia enterocolitica
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- bakteriální adheziny genetika MeSH
- bakteriální chromozomy genetika MeSH
- bakteriální proteiny genetika metabolismus MeSH
- Escherichia coli genetika metabolismus MeSH
- fúze genů MeSH
- genetická transkripce MeSH
- lac operon genetika MeSH
- osmolární koncentrace MeSH
- promotorové oblasti (genetika) MeSH
- regulace genové exprese u bakterií * MeSH
- trans-aktivátory genetika metabolismus MeSH
- Yersinia enterocolitica genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bakteriální adheziny MeSH
- bakteriální proteiny MeSH
- invasin, Yersinia MeSH Prohlížeč
- osmolarity response regulator proteins MeSH Prohlížeč
- trans-aktivátory 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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