Affiliation:
1. Department of Bacteriology, University of Wisconsin, Madison, Wisconsin 53706
Abstract
ABSTRACT
rRNA transcription in
Escherichia coli
is activated by the FIS protein, which binds upstream of
rrnp
1
promoters and interacts directly with RNA polymerase. Analysis of the contribution of FIS to
rrn
transcription under changing physiological conditions is complicated by several factors: the wide variation in cellular FIS concentrations with growth conditions, the contributions of several other regulatory systems to rRNA synthesis, and the pleiotropy of
fis
mutations. In this report, we show by in vivo footprinting and Western blot analysis that occupancy of the
rrnBp
1
FIS sites correlates with cellular levels of FIS. We find, using two methods of measurement (pulse induction of a FIS-activated hybrid promoter and primer extension from an unstable transcript made from
rrnBp
1
), that the extent of transcription activation by FIS parallels the degree of FIS site occupancy and therefore cellular FIS levels. FIS activates transcription throughout exponential growth at low culture density, but
rrnp
1
transcription increases independently of FIS immediately following upshift, before FIS accumulates. These results support the model that FIS is one of a set of overlapping signals that together contribute to transcription from
rrnp
1
promoters during steady-state growth.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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