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Journal of Bacteriology, May 2000, p. 2982-2984, Vol. 182, No. 10
School of Biosciences, The University of
Birmingham, Edgbaston, Birmingham B15 2TT, United
Kingdom1; Institut Pasteur, Unité
de Physico-chimie des Macromolécules Biologiques, 75724 Paris
Cedex 15, France2; Department of
Chemistry, University of California, Davis, California
956163; and Department of Molecular
Genetics, National Institute of Genetics, Mishima, Shizuoka 411, Japan4
Received 10 September 1999/Accepted 12 January 2000
A DNA cleavage reagent, specifically tethered to residue 581 of the
Escherichia coli RNA polymerase
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Positioning of Region 4 of the Escherichia
coli RNA Polymerase
70 Subunit by a
Transcription Activator
70 subunit,
has been used to investigate the location of
70 region 4 in different complexes at the galp1 promoter
and the effect of the cyclic AMP receptor protein. The positions of DNA cleavage by the reagent are not affected by the cyclic AMP receptor protein. We conclude that transcription activation at the
galp1 promoter by the cyclic AMP receptor
protein does not involve major conformation changes in or repositioning
of
70 region 4.
*
Corresponding author. Mailing address: School of
Biosciences, The University of Birmingham, Edgbaston, Birmingham B15
2TT, United Kingdom. Phone: 44-121-414-5439. Fax:
44-121-414-7366. E-mail:
S.J.W.Busby{at}bham.ac.uk.
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