A Transcriptional Regulator of a Pristinamycin Resistance Gene in Streptomyces coelicolor
Pip is apristinamycin-induced transcriptional regulatorprotein detected in many Streptomyces species by its ability to specifically bind sequence motifs within the promoter of a Streptomyces pristinaespiralis multidrug resistance gene (ptr). To investigate the possible role of Pip in regulating mult...
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description | Pip is apristinamycin-induced transcriptional regulatorprotein detected in many Streptomyces species by its ability to specifically bind sequence motifs within the promoter of a Streptomyces pristinaespiralis multidrug resistance gene (ptr). To investigate the possible role of Pip in regulating multidrug resistance, it was purified from a genetically characterized species, Streptomyces coelicolor, utilizing an affinity matrix of the ptr promoter conjugated to magnetic beads. Reverse genetics identified the corresponding locus and confirmed that it encoded Pip, a protein belonging to the TetR family of procaryotic transcriptional repressors. Pip binding motifs were located upstream of the adjacent gene pep, encoding a major facilitator antiporter homologous to ptr. In vivo analysis of antibiotic susceptibility profiles demonstrated that pep conferred elevated levels of resistance only to pristinamycin I (PI), a streptogramin B antibiotic having clinical importance. Purified recombinant Pip was a dimer (in the presence or absence of PI) and displayed a high affinity for its palindromic binding motifs within the ptr promoter and the upstream region of pep. The Pip/ptr promoter complex was dissociated by PI but not by any of the other nonstreptogramin antibiotics that were described previously as transcriptional inducers. These procaryotic regulatory elements served as the basis for the development of systems allowing repression or induction of cloned genes in mammalian and plant cells in response to streptogramin antibiotics (including pristinamycin, virginiamycin, and Synercid®). |
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To investigate the possible role of Pip in regulating multidrug resistance, it was purified from a genetically characterized species, Streptomyces coelicolor, utilizing an affinity matrix of the ptr promoter conjugated to magnetic beads. Reverse genetics identified the corresponding locus and confirmed that it encoded Pip, a protein belonging to the TetR family of procaryotic transcriptional repressors. Pip binding motifs were located upstream of the adjacent gene pep, encoding a major facilitator antiporter homologous to ptr. In vivo analysis of antibiotic susceptibility profiles demonstrated that pep conferred elevated levels of resistance only to pristinamycin I (PI), a streptogramin B antibiotic having clinical importance. Purified recombinant Pip was a dimer (in the presence or absence of PI) and displayed a high affinity for its palindromic binding motifs within the ptr promoter and the upstream region of pep. The Pip/ptr promoter complex was dissociated by PI but not by any of the other nonstreptogramin antibiotics that were described previously as transcriptional inducers. These procaryotic regulatory elements served as the basis for the development of systems allowing repression or induction of cloned genes in mammalian and plant cells in response to streptogramin antibiotics (including pristinamycin, virginiamycin, and Synercid®).</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M007690200</identifier><identifier>PMID: 11050092</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anti-Bacterial Agents - pharmacology ; Bacterial Proteins ; Base Sequence ; Drug Resistance, Microbial - genetics ; Drug Resistance, Multiple - genetics ; Gene Expression Regulation, Bacterial ; Membrane Proteins - genetics ; Molecular Sequence Data ; pep gene ; Peptide Synthases - genetics ; Pip protein ; Pristinamycin ; Promoter Regions, Genetic ; ptr gene ; Repressor Proteins - genetics ; Sequence Alignment ; Sequence Homology, Nucleic Acid ; streptogramin B ; Streptomyces - drug effects ; Streptomyces - genetics ; Streptomyces coelicolor ; Synercid ; TetR protein ; Transcription, Genetic ; virginiamycin ; Virginiamycin - pharmacology</subject><ispartof>The Journal of biological chemistry, 2001-01, Vol.276 (2), p.1479-1485</ispartof><rights>2001 © 2001 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-b87182282cd67de21a269cd195e313fca2cfe40d8d731fd5c79a8e6005d338ab3</citedby><cites>FETCH-LOGICAL-c506t-b87182282cd67de21a269cd195e313fca2cfe40d8d731fd5c79a8e6005d338ab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11050092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Folcher, Marc</creatorcontrib><creatorcontrib>Morris, Rowan P.</creatorcontrib><creatorcontrib>Dale, Glenn</creatorcontrib><creatorcontrib>Salah-Bey-Hocini, Khadidja</creatorcontrib><creatorcontrib>Viollier, Patrick H.</creatorcontrib><creatorcontrib>Thompson, Charles J.</creatorcontrib><title>A Transcriptional Regulator of a Pristinamycin Resistance Gene in Streptomyces coelicolor</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Pip is apristinamycin-induced transcriptional regulatorprotein detected in many Streptomyces species by its ability to specifically bind sequence motifs within the promoter of a Streptomyces pristinaespiralis multidrug resistance gene (ptr). To investigate the possible role of Pip in regulating multidrug resistance, it was purified from a genetically characterized species, Streptomyces coelicolor, utilizing an affinity matrix of the ptr promoter conjugated to magnetic beads. Reverse genetics identified the corresponding locus and confirmed that it encoded Pip, a protein belonging to the TetR family of procaryotic transcriptional repressors. Pip binding motifs were located upstream of the adjacent gene pep, encoding a major facilitator antiporter homologous to ptr. In vivo analysis of antibiotic susceptibility profiles demonstrated that pep conferred elevated levels of resistance only to pristinamycin I (PI), a streptogramin B antibiotic having clinical importance. Purified recombinant Pip was a dimer (in the presence or absence of PI) and displayed a high affinity for its palindromic binding motifs within the ptr promoter and the upstream region of pep. The Pip/ptr promoter complex was dissociated by PI but not by any of the other nonstreptogramin antibiotics that were described previously as transcriptional inducers. These procaryotic regulatory elements served as the basis for the development of systems allowing repression or induction of cloned genes in mammalian and plant cells in response to streptogramin antibiotics (including pristinamycin, virginiamycin, and Synercid®).</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacterial Proteins</subject><subject>Base Sequence</subject><subject>Drug Resistance, Microbial - genetics</subject><subject>Drug Resistance, Multiple - genetics</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Membrane Proteins - genetics</subject><subject>Molecular Sequence Data</subject><subject>pep gene</subject><subject>Peptide Synthases - genetics</subject><subject>Pip protein</subject><subject>Pristinamycin</subject><subject>Promoter Regions, Genetic</subject><subject>ptr gene</subject><subject>Repressor Proteins - genetics</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>streptogramin B</subject><subject>Streptomyces - drug effects</subject><subject>Streptomyces - genetics</subject><subject>Streptomyces coelicolor</subject><subject>Synercid</subject><subject>TetR protein</subject><subject>Transcription, Genetic</subject><subject>virginiamycin</subject><subject>Virginiamycin - pharmacology</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFLxDAQRoMo7rp69Sg9ees6SdomPYroKiiKrqCnkCZTiXSbmnQF_72RXfAkzmWYmTff4RFyTGFOQRRn742Z3wGIqgYGsEOmFCTPeUlfdskUgNG8ZqWckIMY3yFVUdN9MqEUSoCaTcnrebYMuo8muGF0vtdd9ohv606PPmS-zXT2EFwcXa9XX8b16RjTqHuD2QJ7zNLqaQw4jD7dMWbGY-eM73w4JHut7iIebfuMPF9dLi-u89v7xc3F-W1uSqjGvJGCSsYkM7YSFhnVrKqNpXWJnPLWaGZaLMBKKzhtbWlErSVWAKXlXOqGz8jpJncI_mONcVQrFw12ne7Rr6MSUBWiouxfkArBq6KsEzjfgCb4GAO2aghupcOXoqB-rKtkXf1aTw8n2-R1s0L7i281J0BuAEwiPh0GFY3DJNG6gGZU1ru_sr8B9xqRBw</recordid><startdate>20010112</startdate><enddate>20010112</enddate><creator>Folcher, Marc</creator><creator>Morris, Rowan P.</creator><creator>Dale, Glenn</creator><creator>Salah-Bey-Hocini, Khadidja</creator><creator>Viollier, Patrick H.</creator><creator>Thompson, Charles J.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20010112</creationdate><title>A Transcriptional Regulator of a Pristinamycin Resistance Gene in Streptomyces coelicolor</title><author>Folcher, Marc ; Morris, Rowan P. ; Dale, Glenn ; Salah-Bey-Hocini, Khadidja ; Viollier, Patrick H. ; Thompson, Charles J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-b87182282cd67de21a269cd195e313fca2cfe40d8d731fd5c79a8e6005d338ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Bacterial Proteins</topic><topic>Base Sequence</topic><topic>Drug Resistance, Microbial - genetics</topic><topic>Drug Resistance, Multiple - genetics</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Membrane Proteins - genetics</topic><topic>Molecular Sequence Data</topic><topic>pep gene</topic><topic>Peptide Synthases - genetics</topic><topic>Pip protein</topic><topic>Pristinamycin</topic><topic>Promoter Regions, Genetic</topic><topic>ptr gene</topic><topic>Repressor Proteins - genetics</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>streptogramin B</topic><topic>Streptomyces - drug effects</topic><topic>Streptomyces - genetics</topic><topic>Streptomyces coelicolor</topic><topic>Synercid</topic><topic>TetR protein</topic><topic>Transcription, Genetic</topic><topic>virginiamycin</topic><topic>Virginiamycin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Folcher, Marc</creatorcontrib><creatorcontrib>Morris, Rowan P.</creatorcontrib><creatorcontrib>Dale, Glenn</creatorcontrib><creatorcontrib>Salah-Bey-Hocini, Khadidja</creatorcontrib><creatorcontrib>Viollier, Patrick H.</creatorcontrib><creatorcontrib>Thompson, Charles J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Folcher, Marc</au><au>Morris, Rowan P.</au><au>Dale, Glenn</au><au>Salah-Bey-Hocini, Khadidja</au><au>Viollier, Patrick H.</au><au>Thompson, Charles J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Transcriptional Regulator of a Pristinamycin Resistance Gene in Streptomyces coelicolor</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-01-12</date><risdate>2001</risdate><volume>276</volume><issue>2</issue><spage>1479</spage><epage>1485</epage><pages>1479-1485</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Pip is apristinamycin-induced transcriptional regulatorprotein detected in many Streptomyces species by its ability to specifically bind sequence motifs within the promoter of a Streptomyces pristinaespiralis multidrug resistance gene (ptr). To investigate the possible role of Pip in regulating multidrug resistance, it was purified from a genetically characterized species, Streptomyces coelicolor, utilizing an affinity matrix of the ptr promoter conjugated to magnetic beads. Reverse genetics identified the corresponding locus and confirmed that it encoded Pip, a protein belonging to the TetR family of procaryotic transcriptional repressors. Pip binding motifs were located upstream of the adjacent gene pep, encoding a major facilitator antiporter homologous to ptr. In vivo analysis of antibiotic susceptibility profiles demonstrated that pep conferred elevated levels of resistance only to pristinamycin I (PI), a streptogramin B antibiotic having clinical importance. Purified recombinant Pip was a dimer (in the presence or absence of PI) and displayed a high affinity for its palindromic binding motifs within the ptr promoter and the upstream region of pep. The Pip/ptr promoter complex was dissociated by PI but not by any of the other nonstreptogramin antibiotics that were described previously as transcriptional inducers. These procaryotic regulatory elements served as the basis for the development of systems allowing repression or induction of cloned genes in mammalian and plant cells in response to streptogramin antibiotics (including pristinamycin, virginiamycin, and Synercid®).</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11050092</pmid><doi>10.1074/jbc.M007690200</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents - pharmacology Bacterial Proteins Base Sequence Drug Resistance, Microbial - genetics Drug Resistance, Multiple - genetics Gene Expression Regulation, Bacterial Membrane Proteins - genetics Molecular Sequence Data pep gene Peptide Synthases - genetics Pip protein Pristinamycin Promoter Regions, Genetic ptr gene Repressor Proteins - genetics Sequence Alignment Sequence Homology, Nucleic Acid streptogramin B Streptomyces - drug effects Streptomyces - genetics Streptomyces coelicolor Synercid TetR protein Transcription, Genetic virginiamycin Virginiamycin - pharmacology |
title | A Transcriptional Regulator of a Pristinamycin Resistance Gene in Streptomyces coelicolor |
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