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J. Bacteriol., 12 1995, 6704-6710, Vol 177, No. 23
HJ Wing, SM Williams and SJ Busby
We cloned a consensus DNA site for the Escherichia coli FNR protein at
different locations upstream of the E. coli melR promoter. FNR can activate
transcription initiation at the melR promoter when the FNR binding site is
centered around 41, 61, 71, 82, and 92 bp upstream from the transcription
start. The SF73 positive control amino acid substitution in FNR interfered
with transcription activation by FNR in each case. In contrast, the GA85
positive control substitution reduced activation only at the promoter,
where the FNR binding site is 41 bp upstream of the transcript start. The
SF73 substitution appears to identify an activating region of FNR that is
important for transcription activation at promoters that differ in
architecture. Experiments with oriented heterodimers showed that this
activating region is functional in the upstream subunit of the FNR dimer at
the promoter where FNR binds around 41 bp from the transcript start and in
the downstream subunit at the promoters where FNR binds farther upstream.
Copyright © 1995, American Society for Microbiology
Spacing requirements for transcription activation by Escherichia coli FNR protein
School of Biochemistry, University of Birmingham, United Kingdom.
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