Activation by NarL at the Escherichia coli ogt promoter

Author:

Ruanto Patcharawarin1,Chismon David L.1,Hothersall Joanne1,Godfrey Rita E.1,Lee David J.12,Busby Stephen J. W.1,Browning Douglas F.1ORCID

Affiliation:

1. Institute of Microbiology and Infection and School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.

2. Department of Life Sciences, School of Health Sciences, Birmingham City University, Birmingham B15 3TN, U.K.

Abstract

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 O6-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.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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