Identification of a distantly located regulatory element in the luxD gene required for negative autoregulation of the Vibrio fischeri luxR gene

Expression of bioluminescence in the marine bacterium Vibrio fischeri is controlled by a unique cell density-dependent regulatory mechanism called auto-induction. The genes required for bioluminescence (the lux genes) are organized in two divergently transcribed operons (luxR-luxICDABEG). One operon...

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Veröffentlicht in:The Journal of biological chemistry 1992-04, Vol.267 (11), p.7690-7695
Hauptverfasser: SHADEL, G. S, BALDWIN, T. O
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description Expression of bioluminescence in the marine bacterium Vibrio fischeri is controlled by a unique cell density-dependent regulatory mechanism called auto-induction. The genes required for bioluminescence (the lux genes) are organized in two divergently transcribed operons (luxR-luxICDABEG). One operon (luxICDABEG) contains the genes required for light production (luxCDABE) and the synthesis of a diffusible signal molecule called autoinducer (luxI). The other operon contains the luxR gene which encodes a transcriptional regulatory protein that activates transcription of both lux operons in the presence of autoinducer. This bidirectional stimulatory mechanism leads to a positive feedback circuit that results in a rapid increase in light production at a particular culture cell density which is characteristic of autoinduction. Transcriptional positive feedback is apparently limited by a negative autoregulatory circuit through which LuxR acts to inhibit its own synthesis. Transcriptional negative autoregulation requires autoinducer, the lux operator located in the control region (which is the binding site for LuxR), and negative acting DNA sequences in the luxICDABEG operon. Deletion analysis of the luxICDABEG operon demonstrated that a negative acting element is located in the luxD gene at a position 2.0 kilobases from the lux operator. The nucleotide sequence of this luxD element is similar to the lux operator (11 of 20 base pairs identical) and can function as a LuxR-binding site when it replaces the lux operator in the control region. These results suggest that the luxD element functions as a low affinity binding site for LuxR and that occupancy of this site is required to achieve transcriptional negative autoregulation of luxR.
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Transcriptional positive feedback is apparently limited by a negative autoregulatory circuit through which LuxR acts to inhibit its own synthesis. Transcriptional negative autoregulation requires autoinducer, the lux operator located in the control region (which is the binding site for LuxR), and negative acting DNA sequences in the luxICDABEG operon. Deletion analysis of the luxICDABEG operon demonstrated that a negative acting element is located in the luxD gene at a position 2.0 kilobases from the lux operator. The nucleotide sequence of this luxD element is similar to the lux operator (11 of 20 base pairs identical) and can function as a LuxR-binding site when it replaces the lux operator in the control region. 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One operon (luxICDABEG) contains the genes required for light production (luxCDABE) and the synthesis of a diffusible signal molecule called autoinducer (luxI). The other operon contains the luxR gene which encodes a transcriptional regulatory protein that activates transcription of both lux operons in the presence of autoinducer. This bidirectional stimulatory mechanism leads to a positive feedback circuit that results in a rapid increase in light production at a particular culture cell density which is characteristic of autoinduction. Transcriptional positive feedback is apparently limited by a negative autoregulatory circuit through which LuxR acts to inhibit its own synthesis. Transcriptional negative autoregulation requires autoinducer, the lux operator located in the control region (which is the binding site for LuxR), and negative acting DNA sequences in the luxICDABEG operon. Deletion analysis of the luxICDABEG operon demonstrated that a negative acting element is located in the luxD gene at a position 2.0 kilobases from the lux operator. The nucleotide sequence of this luxD element is similar to the lux operator (11 of 20 base pairs identical) and can function as a LuxR-binding site when it replaces the lux operator in the control region. These results suggest that the luxD element functions as a low affinity binding site for LuxR and that occupancy of this site is required to achieve transcriptional negative autoregulation of luxR.</abstract><cop>Bethesda, MD</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>1560004</pmid><doi>10.1016/S0021-9258(18)42570-7</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Bacterial Proteins - genetics
Base Sequence
Biological and medical sciences
Chromosome Deletion
DNA, Bacterial
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Bacterial
Genes, Bacterial
Marine
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Mutagenesis, Site-Directed
Operon
Plasmids
Regulatory Sequences, Nucleic Acid
Repressor Proteins
Trans-Activators
Transcription Factors - genetics
Transcription, Genetic
Transcription. Transcription factor. Splicing. Rna processing
Vibrio - genetics
Vibrio fischeri
title Identification of a distantly located regulatory element in the luxD gene required for negative autoregulation of the Vibrio fischeri luxR gene
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