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 |
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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. |
doi_str_mv | 10.1016/S0021-9258(18)42570-7 |
format | Article |
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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.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(18)42570-7</identifier><identifier>PMID: 1560004</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Biochemistry and Molecular Biology</publisher><subject>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</subject><ispartof>The Journal of biological chemistry, 1992-04, Vol.267 (11), p.7690-7695</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-f43a6943d90a681c00f26ec467d22891e4908a4bb9e31809d6c1f208a1d350753</citedby><cites>FETCH-LOGICAL-c439t-f43a6943d90a681c00f26ec467d22891e4908a4bb9e31809d6c1f208a1d350753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5290480$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1560004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SHADEL, G. S</creatorcontrib><creatorcontrib>BALDWIN, T. O</creatorcontrib><title>Identification of a distantly located regulatory element in the luxD gene required for negative autoregulation of the Vibrio fischeri luxR gene</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><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.</description><subject>Bacterial Proteins - genetics</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosome Deletion</subject><subject>DNA, Bacterial</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes, Bacterial</subject><subject>Marine</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis, Site-Directed</subject><subject>Operon</subject><subject>Plasmids</subject><subject>Regulatory Sequences, Nucleic Acid</subject><subject>Repressor Proteins</subject><subject>Trans-Activators</subject><subject>Transcription Factors - genetics</subject><subject>Transcription, Genetic</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><subject>Vibrio - genetics</subject><subject>Vibrio fischeri</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkd1u1DAQhS1EVZbCI1SyBEJwEfDYjhNfovLTSpWQ-BN3lpOMd42SuLUT2n0KXhlnsyq-sTXznTPWGULOgb0FBurdN8Y4FJqX9Wuo30heVqyoHpENsFoUooRfj8nmAXlCnqb0m-UjNZySUyjV8t6Qv1cdjpN3vrWTDyMNjlra-TTZcer3tA-5jh2NuJ17O4W4p9jjkCXUj3TaIe3n-w90iyNm5nb2McMuRDriNhv-QWrnrFrVR_9F9dM30QfqfGp3GP3i8vXg8oycONsnfH68z8iPTx-_X1wW118-X128vy5aKfRUOCms0lJ0mllVQ8uY4wpbqaqO81oDSs1qK5tGo4Ca6U614HguQSdKVpXijLxafW9iuJ0xTWbIf8G-tyOGORlQIEHoBSxXsI0hpYjO3EQ_2Lg3wMyyCHNYhFlSNlCbwyJMlXXnxwFzM2D3X7Umn_svj32bWtu7aMfWpwes5JrJmmXsxYrt_HZ3l-M1jQ85s8FwVRkAUynNxD-bt53a</recordid><startdate>19920415</startdate><enddate>19920415</enddate><creator>SHADEL, G. S</creator><creator>BALDWIN, T. 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O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-f43a6943d90a681c00f26ec467d22891e4908a4bb9e31809d6c1f208a1d350753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosome Deletion</topic><topic>DNA, Bacterial</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genes, Bacterial</topic><topic>Marine</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis, Site-Directed</topic><topic>Operon</topic><topic>Plasmids</topic><topic>Regulatory Sequences, Nucleic Acid</topic><topic>Repressor Proteins</topic><topic>Trans-Activators</topic><topic>Transcription Factors - genetics</topic><topic>Transcription, Genetic</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><topic>Vibrio - genetics</topic><topic>Vibrio fischeri</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHADEL, G. S</creatorcontrib><creatorcontrib>BALDWIN, T. O</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SHADEL, G. S</au><au>BALDWIN, T. O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a distantly located regulatory element in the luxD gene required for negative autoregulation of the Vibrio fischeri luxR gene</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1992-04-15</date><risdate>1992</risdate><volume>267</volume><issue>11</issue><spage>7690</spage><epage>7695</epage><pages>7690-7695</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>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.</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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ispartof | The Journal of biological chemistry, 1992-04, Vol.267 (11), p.7690-7695 |
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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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