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Journal of Bacteriology, February 1999, p. 1269-1280, Vol. 181, No. 4
Department of Biological Sciences, University
at Albany, SUNY, Albany, New York
Received 24 August 1998/Accepted 30 November 1998
Escherichia coli Fis is a small DNA binding and bending
protein that has been implicated in a variety of biological processes. A minimal promoter sequence consisting of 43 bp is sufficient to
generate its characteristic growth phase-dependent expression pattern
and is also subject to negative regulation by stringent control.
However, information about the precise identification of nucleotides
contributing to basal promoter activity and its regulation has been
scant. In this work, 72 independent mutations were generated in the
fis promoter (fis P) region from
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Functional Determinants of the Escherichia
coli fis Promoter: Roles of
35,
10, and Transcription
Initiation Regions in the Response to Stringent Control and Growth
Phase-Dependent Regulation
108 to +78
using both random and site-directed PCR mutagenesis.
-Galactosidase activities from mutant promoters fused to the
(trp-lac)W200 fusion on a plasmid were used to
conclusively identify the sequences TTTCAT and TAATAT as the
35 and
10 regions, respectively, which are optimally separated by 17 bp. We
found that four consecutive substitutions within the GC-rich sequence
just upstream of +1 and mutations in the
35 region, but not in the
10 region, significantly reduced the response to stringent control.
Analysis of the effects of mutations on growth phase-dependent
regulation showed that replacing the predominant transcription
initiation nucleotide +1C with a preferred nucleotide (A or G)
profoundly altered expression such that high levels of fis
P mRNA were detected during late logarithmic and early stationary
phases. A less dramatic effect was seen with improvements in the
10
and
35 consensus sequences. These results suggest that the acute
growth phase-dependent regulation pattern observed with this promoter
requires an inefficient transcription initiation process that is
achieved with promoter sequences deviating from the
10 and
35
consensus sequences and, more importantly, a dependence upon the
availability of the least favored transcription initiation nucleotide, CTP.
*
Corresponding author. Mailing address: Department of
Biological Sciences, University at Albany, SUNY, 1400 Washington Ave., Albany, NY 12222. Phone: (518) 442-4333. Fax: (518) 442-4767. E-mail:
osuna{at}cnsunix.albany.edu.
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