DNase I protection of the plasmid-borne clcABD promoter and chromosomal catBC promoter generated a binding footprint for ClcR on each. EMSA confirmed binding to these regions. Qualitative growth analysis and beta-gal assay demonstrated that despite confirmed binding to the catBC promoter, clcR did not activate its transcription.
Regulated genes for each binding site are displayed below. Gene regulation diagrams show binding sites, positively-regulated genes, negatively-regulated genes, both positively and negatively regulated genes, genes with unspecified type of regulation. For each indvidual site, experimental techniques used to determine the site are also given.
Site sequence | Regulated genes | Gene diagram | Experimental techniques | TF function | TF type |
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