The role of FIS in trans activation of stable RNA operons of E. coli.
Open Access
- 1 March 1990
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 9 (3) , 727-734
- https://doi.org/10.1002/j.1460-2075.1990.tb08166.x
Abstract
The thrU(tufB) operon of Escherichia coli is endowed with a cis‐acting region upstream of the promoter, designated UAS for Upstream Activator Sequence. A protein fraction has been isolated that binds specifically to DNA fragments of the UAS, thus forming three protein‐DNA complexes corresponding to three binding sites on the UAS. It stimulates in vitro transcription of the operon by facilitating the binding of the RNA polymerase to the promoter. All three protein‐DNA complexes contain one and the same protein. Dissociation constants for the three complexes have been determined, the lowest being in the sub‐nanomolar range. The protein also binds to the UAS of the tyrT operon and to the UAS upstream of the P1 promoter of the rrnB operon, suggesting that transcription of the three operons, if not of more stable RNA operons, is activated by a common trans activator. We demonstrate that the E.coli protein FIS (Factor for Inversion Stimulation) also binds to the UAS of the thrU(tufB) operon forming three protein‐DNA complexes. A burst of UAS‐ and FIS‐dependent promoter activity is observed after reinitiation of growth of stationary cultures in fresh medium.This publication has 29 references indexed in Scilit:
- Bent DNA is needed for recombinational enhancer activity in the site-specific recombination system cin of bacteriophage P1 the role of FIS proteinJournal of Molecular Biology, 1989
- Purification and DNA-binding properties of FIS and Cin, two proteins required for the bacteriophage P1 site-specific recombination system, cinJournal of Molecular Biology, 1987
- The tRNA-tufB operon transcription termination and processing upstream from tufBJournal of Molecular Biology, 1987
- Cellular factors couple recombination with growth phase: Characterization of a new component in the λ site-specific recombination pathwayCell, 1987
- Host protein requirements for in vitro site-specific DNA inversionCell, 1986
- DNA determinants of rRNA synthesis in E. coli: Growth rate dependent regulation, feedback inhibition, upstream activation, antiterminationCell, 1986
- Hin-mediated site-specific recombination requires two 26 by recombination sites and a 60 by recombinational enhancerCell, 1985
- G inversion in bacteriophage Mu DNA is stimulated by a site within the invertase gene and a host factorCell, 1985
- Genetically separable functional elements mediate the optimal expression and stringent regulation of a bacterial tRNA geneCell, 1985
- Control of Ribosomal RNA Synthesis in vitroNature, 1973