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Nucleic Acids Research Advance Access originally published online on March 16, 2008
Nucleic Acids Research 2008 36(8):2667-2676; doi:10.1093/nar/gkn119
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Nucleic Acids Research, 2008, Vol. 36, No. 8 2667-2676
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Molecular Biology

Autoregulation of the Escherichia coli melR promoter: repression involves four molecules of MelR

Shivanthi Samarasinghe1, Mohamed Samir El-Robh1, David C. Grainger1, Wenke Zhang2, Panos Soultanas2 and Stephen J. W. Busby1,*

1School of Biosciences, The University of Birmingham, Edgbaston, Birmingham B15 2TT and 2The University of Nottingham, Centre for Biomolecular Sciences, University Park, Nottingham NG7 2RD, UK

*To whom correspondence should be addressed. Tel: (+44) 121 414 5439; Fax: (+44) 121 414 5925; Email: s.j.w.busby{at}bham.ac.uk

Received December 20, 2007. Revised February 29, 2008. Accepted March 3, 2008.

The Escherichia coli MelR protein is a transcription activator that autoregulates its own promoter by repressing transcription initiation. Optimal repression requires MelR binding to a site that overlaps the melR transcription start point and to upstream sites. In this work, we have investigated the different determinants needed for optimal repression and their spatial requirements. We show that repression requires a complex involving four DNA-bound MelR molecules, and that the global CRP regulator plays little or no role.


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