Summary:
The "Rhamnose regulator," RhaR, is a transcription factor that regulates genes involved in L-rhamnose degradation and coregulates with the global transcriptional regulator CRP. These regulators bind cooperatively to activate transcription of the unusual operon rhaSR, which encodes two transcriptional regulators, RhaS and RhaR (30% identical), both members of the AraC/XylS family of transcriptional regulators and involved in L-rhamnose transport and degradation [3, 8]. In vitro transcription assays indicate that the α-CTD of the RNA polymerase is partially dispensable for RhaR activation and is required for CRP activation of the rhaSR operon [3, 8].
Apparently, expression of the operons involved in transport and degradation of L-rhamnose first requires expression of RhaR, which induces transcription of the rhaSR operon. In this way, RhaS activates transcription of L-rhamnose gene clusters.
Transcription of the rhaSR operon is induced when E. coli is grown on L-rhamnose in the absence of glucose. Gene induction occurs when the physiological inducer, L-rhamnose, binds to RhaR and when cellular cyclic AMP levels are high [3, 8].
This transcription factor is composed of two domains, a C-terminal domain that contains two potential helix-turn-helix DNA-binding motifs and an N-terminal domain involved in l-rhamnose binding and dimerization of the protein [2, 4, 9].
In the presence of L-rhamnose, RhaR binds in tandem to two repeat sequences upstream of the
rhaS intergenic region to activate transcription by overlapping the -35 box of
rhaSp. The binding targets for RhaR consist of 17-nucleotide-long sequences that possess conserved motifs; each monomer binds to one of these conserved sequences located on different faces of the DNA
[8].
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