@article{mbs:/content/journal/micro/10.1099/mic.0.27734-0, author = "Yang, Ji and Tauschek, Marija and Strugnell, Richard and Robins-Browne, Roy M.", title = "The H-NS protein represses transcription of the eltAB operon, which encodes heat-labile enterotoxin in enterotoxigenic Escherichia coli, by binding to regions downstream of the promoter", journal= "Microbiology", year = "2005", volume = "151", number = "4", pages = "1199-1208", doi = "https://doi.org/10.1099/mic.0.27734-0", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.27734-0", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "LT, heat-labile enterotoxin", keywords = "EMSA, electrophoretic mobility shift assay", keywords = "EPEC, enteropathogenic Escherichia coli", keywords = "H-NS protein, heat-stable nucleoid-structural protein", keywords = "ETEC, enterotoxigenic E. coli", keywords = "CT, cholera toxin", keywords = "DRE, downstream regulatory element", abstract = "Heat-labile enterotoxin, a major virulence determinant of enterotoxigenic Escherichia coli, is encoded by the eltAB operon. To elucidate the molecular mechanism by which the heat-stable nucleoid-structural (H-NS) protein controls transcription of eltAB, the authors constructed an eltAB–lacZ transcriptional fusion and performed β-galactosidase analysis. The results showed that H-NS protein exerts fivefold repression on transcription from the eltAB promoter at 37 °C and 10-fold repression at 22 °C. Two silencer regions that were required for H-NS-mediated repression of eltAB expression were identified, both of which were located downstream of the start site of transcription. One silencer was located between +31 and +110, the other between +460 and +556, relative to the start site of transcription, and they worked cooperatively in repression. DNA sequences containing the silencers were predicted to be curved by in silico analysis and bound H-NS protein directly in vitro. Repression of eltAB transcription by H-NS was independent of promoter strength, and the presence of H-NS protein did not affect promoter opening in vitro, indicating that repression was achieved by inhibiting promoter clearance or blocking transcription elongation, probably via DNA looping between the two silencers.", }