Activation of Escherichia coli rRNA Transcription by FIS during a Growth Cycle

Author:

Appleman J. Alex1,Ross Wilma1,Salomon Julia1,Gourse Richard L.1

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

Reference54 articles.

1. Appleman J. A. and R. L. Gourse. Unpublished results.

2. Bachmann B. J. Linkage map of Escherichia coli K-12 edition 7 Escherichia coli and Salmonella typhimurium: cellular and molecular biology. Neidhardt F. C. Ingraham J. L. Low K. B. Magasanik B. Schaechter M. Umbarger H. E. 1987 807 876 American Society for Microbiology Washington D.C

3. Dramatic changes in Fis levels upon nutrient upshift in Escherichia coli

4. Bartlett M. T. Gaal W. Ross and R. L. Gourse. RNA polymerase mutants defective in the NTP-sensing mechanism for growth rate-dependent control of rRNA transcription. Submitted for publication.

5. Growth rate-dependent control of the rrnB P1 core promoter in Escherichia coli

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