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Activation by NarL at the Escherichia coli ogt promoter

The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which control...

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Autores principales: Ruanto, Patcharawarin, Chismon, David L., Hothersall, Joanne, Godfrey, Rita E., Lee, David J., Busby, Stephen J. W., Browning, Douglas F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419079/
https://www.ncbi.nlm.nih.gov/pubmed/32662815
http://dx.doi.org/10.1042/BCJ20200408
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author Ruanto, Patcharawarin
Chismon, David L.
Hothersall, Joanne
Godfrey, Rita E.
Lee, David J.
Busby, Stephen J. W.
Browning, Douglas F.
author_facet Ruanto, Patcharawarin
Chismon, David L.
Hothersall, Joanne
Godfrey, Rita E.
Lee, David J.
Busby, Stephen J. W.
Browning, Douglas F.
author_sort Ruanto, Patcharawarin
collection PubMed
description The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which controls the expression of an O(6)-alkylguanine-DNA-alkyltransferase, is dependent on NarL binding to two DNA targets centred at positions −44.5 and −77.5 upstream from the transcript start. Here, we describe ogt promoter derivatives that can be activated solely by NarL binding either at position −44.5 or position −77.5. We show that NarL can also activate the ogt promoter when located at position −67.5. We present data to argue that NarL-dependent activation of transcript initiation at the ogt promoter results from a direct interaction between NarL and a determinant in the C-terminal domain of the RNA polymerase α subunit. Footprinting experiments show that, at the −44.5 promoter, NarL and the C-terminal domain of the RNA polymerase α subunit bind to opposite faces of promoter DNA, suggesting an unusual mechanism of transcription activation. Our work suggests new organisations for activator-dependent transcription at promoters and future applications for biotechnology.
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spelling pubmed-74190792020-08-19 Activation by NarL at the Escherichia coli ogt promoter Ruanto, Patcharawarin Chismon, David L. Hothersall, Joanne Godfrey, Rita E. Lee, David J. Busby, Stephen J. W. Browning, Douglas F. Biochem J Gene Expression & Regulation The Escherichia coli NarX/NarL two-component response-regulator system regulates gene expression in response to nitrate ions and the NarL protein is a global transcription factor, which activates transcript initiation at many target promoters. One such target, the E. coli ogt promoter, which controls the expression of an O(6)-alkylguanine-DNA-alkyltransferase, is dependent on NarL binding to two DNA targets centred at positions −44.5 and −77.5 upstream from the transcript start. Here, we describe ogt promoter derivatives that can be activated solely by NarL binding either at position −44.5 or position −77.5. We show that NarL can also activate the ogt promoter when located at position −67.5. We present data to argue that NarL-dependent activation of transcript initiation at the ogt promoter results from a direct interaction between NarL and a determinant in the C-terminal domain of the RNA polymerase α subunit. Footprinting experiments show that, at the −44.5 promoter, NarL and the C-terminal domain of the RNA polymerase α subunit bind to opposite faces of promoter DNA, suggesting an unusual mechanism of transcription activation. Our work suggests new organisations for activator-dependent transcription at promoters and future applications for biotechnology. Portland Press Ltd. 2020-08-14 2020-08-07 /pmc/articles/PMC7419079/ /pubmed/32662815 http://dx.doi.org/10.1042/BCJ20200408 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Birmingham in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC.
spellingShingle Gene Expression & Regulation
Ruanto, Patcharawarin
Chismon, David L.
Hothersall, Joanne
Godfrey, Rita E.
Lee, David J.
Busby, Stephen J. W.
Browning, Douglas F.
Activation by NarL at the Escherichia coli ogt promoter
title Activation by NarL at the Escherichia coli ogt promoter
title_full Activation by NarL at the Escherichia coli ogt promoter
title_fullStr Activation by NarL at the Escherichia coli ogt promoter
title_full_unstemmed Activation by NarL at the Escherichia coli ogt promoter
title_short Activation by NarL at the Escherichia coli ogt promoter
title_sort activation by narl at the escherichia coli ogt promoter
topic Gene Expression & Regulation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419079/
https://www.ncbi.nlm.nih.gov/pubmed/32662815
http://dx.doi.org/10.1042/BCJ20200408
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