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FEMS Microbiol Lett ; 257(1): 99-105, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16553838

ABSTRACT

A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a sigma54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at -55 with respect to the transcription start site (+1). Binding of FIS at this site activates the transcription of glnAp2 both in vivo and in vitro. Furthermore, we substituted the FIS-mediated DNA bending with other protein (cAMP receptor protein or integration host factor)-mediated DNA bending, without changing the position of the bending center. In vitro transcription assays indicated that all DNA bends centered at -55 activate transcriptional initiation of glnAp2, especially when linear templates were used.


Subject(s)
DNA, Bacterial/metabolism , Escherichia coli/metabolism , Factor For Inversion Stimulation Protein/metabolism , Gene Expression Regulation, Bacterial , Glutamate-Ammonia Ligase/metabolism , Base Sequence , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Enhancer Elements, Genetic , Escherichia coli/genetics , Escherichia coli Proteins/genetics , Escherichia coli Proteins/metabolism , Factor For Inversion Stimulation Protein/genetics , Glutamate-Ammonia Ligase/chemistry , Glutamate-Ammonia Ligase/genetics , Molecular Sequence Data , Nucleic Acid Conformation , Promoter Regions, Genetic , Transcription, Genetic
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