PMID:11160809
| Citation |
Ozaki, T, Kumaki, Y, Kitagawa, R and Ogawa, T (2001) Anomalous DnaA protein binding to the regulatory region of the Escherichia coli aldA gene. Microbiology (Reading, Engl.) 147:153-9 |
|---|---|
| Abstract |
A binding site for DnaA protein was identified in the regulatory region of the aldA gene of Escherichia coli. Specific binding was demonstrated by in vitro assays including filter binding as well as mobility shift in a polyacrylamide gel of the DnaA-DNA complex. In cells growing in minimal medium containing glucose, expression of ss-galactosidase activity from an aldA-lacZ fusion gene was suppressed by oversupply of DnaA protein and was enhanced by reducing the free DnaA level. These results suggest that DnaA protein negatively regulates expression of the aldA gene under these conditions. Despite fairly strong binding, the bound DNA fragment had no consensus 9 bp DnaA binding sequence (DnaA box), and anomalous binding to an AT-rich sequence located close to the transcription start site was revealed by a footprinting experiment. |
| Links | |
| Keywords |
Aldehyde Dehydrogenase/genetics; Aldehyde Dehydrogenase/metabolism; Bacterial Proteins/genetics; Bacterial Proteins/metabolism; Base Sequence; Binding Sites/genetics; DNA Footprinting/methods; DNA Replication; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; Deoxyribonuclease I/metabolism; Escherichia coli/genetics; Escherichia coli/metabolism; Gene Expression Regulation, Bacterial; Molecular Sequence Data; Regulatory Sequences, Nucleic Acid/genetics; Regulatory Sequences, Nucleic Acid/physiology |
| edit table |
Significance
You can help EcoliWiki by summarizing why this paper is useful
Useful Materials and Methods
You can help Ecoliwiki by describing the useful materials (strains, plasmids, antibodies, etc) described in this paper.
Annotations
<annotationlinks/>
EcoliWiki Links
Add links to pages that link here (e.g. gene, product, method pages)
References
See Help:References for how to manage references in EcoliWiki.