Activation of transcription at divergent urea-dependent promoters by the urease gene regulator UreR

• Published in: Molecular microbiology Vol. 21; no. 3; p. 643
• Main Authors: D'Orazio, S E, Thomas, V, Collins, C M
• Format: Journal Article
• Language: English
• Published: England 01.08.1996
• Subjects: Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Base Sequence; Binding Sites; Chromosome Mapping; DNA, Bacterial; Molecular Sequence Data; Peptide Chain Initiation, Translational; Plasmids; Promoter Regions, Genetic; Proteus mirabilis - drug effects; Proteus mirabilis - enzymology; Sequence Homology, Nucleic Acid; Transcriptional Activation; Urea - pharmacology; Urease - genetics; Urease - metabolism
• ISSN: 0950-382X
• DOI: 10.1111/j.1365-2958.1996.tb02572.x

The Proteus mirabilis and plasmid-encoded urease loci contain seven contiguous structural and accessory genes (ureDABCEFG) and the divergently transcribed ureR, which codes for an AraC-like transcriptional activator. Previously, it was shown that the plasmid-encoded ureR to ureD intergenic region contained divergent promoters (ureRp and ureDp). Transcription from these promoters required both the effector molecule urea and the activator protein UreR. In this report, we demonstrate that the P. mirabilis urease gene cluster contains similar divergent urea- and UreR-dependent promoters. The ureR gene products from either urease locus were able to activate transcription at both the plasmid-encoded and P. mirabilis promoters. The minimal concentration of urea required to activate transcription at ureRp or ureDp from either gene cluster was approximately 4 mM. The transcriptional start sites for the plasmid-encoded and P. mirabilis divergent promoters were similar in an Escherichia coli DH5 alpha background, as determined by primer-extension analysis. However, in P. mirabilis HI4320, transcription of ureR initiated predominately at an alternative site. Physical mapping and inhibition studies were used to localize the UreR-binding sites within the plasmid-encoded ureRp and ureDp intergenic sequences to regions of 68 bp and 86 bp, respectively. Gel shift analysis demonstrated that UreR bound to a 135 bp fragment in the approximate centre of the plasmid-encoded ureR to ureD intergenic region. The results presented here suggest that the P. mirabilis and plasmid-encoded urease gene clusters utilize similar mechanisms of transcriptional activation in response to urea.