Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions
Macromolecular interactions define many biological phenomena. Although genetic methods are available to identify novel protein-protein and DNA-protein interactions, no genetic system has thus far been described to identify molecules or mutations that dissociate known interactions. Herein, we describ...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1996-09, Vol.93 (19), p.10315-10320 |
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creator | Vidal, Marc Brachmann, Rainer K. Fattaey, Ali Harlow, Ed Boeke, Jef D. |
description | Macromolecular interactions define many biological phenomena. Although genetic methods are available to identify novel protein-protein and DNA-protein interactions, no genetic system has thus far been described to identify molecules or mutations that dissociate known interactions. Herein, we describe genetic systems that detect such events in the yeast Saccharomyces cerevisiae. We have engineered yeast strains in which the interaction of two proteins expressed in the context of the two-hybrid system or the interaction between a DNA-binding protein and its binding site in the context of the one-hybrid system is deleterious to growth. Under these conditions, dissociation of the interaction provides a selective growth advantage, thereby facilitating detection. These methods referred to as the ``reverse two-hybrid system'' and ``reverse one-hybrid system'' facilitate the study of the structure-function relationships and regulation of protein-protein and DNA-protein interactions. They should also facilitate the selection of dissociator molecules that could be used as therapeutic agents. |
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Although genetic methods are available to identify novel protein-protein and DNA-protein interactions, no genetic system has thus far been described to identify molecules or mutations that dissociate known interactions. Herein, we describe genetic systems that detect such events in the yeast Saccharomyces cerevisiae. We have engineered yeast strains in which the interaction of two proteins expressed in the context of the two-hybrid system or the interaction between a DNA-binding protein and its binding site in the context of the one-hybrid system is deleterious to growth. Under these conditions, dissociation of the interaction provides a selective growth advantage, thereby facilitating detection. These methods referred to as the ``reverse two-hybrid system'' and ``reverse one-hybrid system'' facilitate the study of the structure-function relationships and regulation of protein-protein and DNA-protein interactions. They should also facilitate the selection of dissociator molecules that could be used as therapeutic agents.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.93.19.10315</identifier><identifier>PMID: 8816797</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Alleles ; Base Sequence ; Binding Sites ; Blotting, Western ; Consensus Sequence ; Deoxyribonucleic acid ; DNA ; DNA Primers ; DNA, Fungal - metabolism ; DNA-Binding Proteins - metabolism ; Drug interactions ; Fungal Proteins - biosynthesis ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Genes, Reporter ; Genetic mutation ; Genetics ; Medical genetics ; Models, Genetic ; Molecular Sequence Data ; Molecules ; Mutation ; Phenotypes ; Plasmids ; Polymerase Chain Reaction ; Promoter Regions, Genetic ; Protein Multimerization ; Proteins ; Recombinant Proteins - biosynthesis ; Reporter genes ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - growth & development ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins ; Transcription Factors ; Two-Hybrid System Techniques ; Yeast ; Yeasts</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1996-09, Vol.93 (19), p.10315-10320</ispartof><rights>Copyright 1996 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Sep 17, 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-708ba68758ccbfef343ce3e6107ee4304cf992ed4dbf235f600402f84c266f7b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/93/19.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/40382$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/40382$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8816797$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vidal, Marc</creatorcontrib><creatorcontrib>Brachmann, Rainer K.</creatorcontrib><creatorcontrib>Fattaey, Ali</creatorcontrib><creatorcontrib>Harlow, Ed</creatorcontrib><creatorcontrib>Boeke, Jef D.</creatorcontrib><title>Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Macromolecular interactions define many biological phenomena. Although genetic methods are available to identify novel protein-protein and DNA-protein interactions, no genetic system has thus far been described to identify molecules or mutations that dissociate known interactions. Herein, we describe genetic systems that detect such events in the yeast Saccharomyces cerevisiae. We have engineered yeast strains in which the interaction of two proteins expressed in the context of the two-hybrid system or the interaction between a DNA-binding protein and its binding site in the context of the one-hybrid system is deleterious to growth. Under these conditions, dissociation of the interaction provides a selective growth advantage, thereby facilitating detection. These methods referred to as the ``reverse two-hybrid system'' and ``reverse one-hybrid system'' facilitate the study of the structure-function relationships and regulation of protein-protein and DNA-protein interactions. They should also facilitate the selection of dissociator molecules that could be used as therapeutic agents.</description><subject>Alleles</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Blotting, Western</subject><subject>Consensus Sequence</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Primers</subject><subject>DNA, Fungal - metabolism</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Drug interactions</subject><subject>Fungal Proteins - biosynthesis</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Genes, Reporter</subject><subject>Genetic mutation</subject><subject>Genetics</subject><subject>Medical genetics</subject><subject>Models, Genetic</subject><subject>Molecular Sequence Data</subject><subject>Molecules</subject><subject>Mutation</subject><subject>Phenotypes</subject><subject>Plasmids</subject><subject>Polymerase Chain Reaction</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Multimerization</subject><subject>Proteins</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Reporter genes</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - growth & development</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Transcription Factors</subject><subject>Two-Hybrid System Techniques</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EKsvCHSEhIg6ISxZ_JbYlLlUXaKWKIihny3HGkFXWXmxv2_3vSbrpinKA02j0fm8844fQc4IXBAv2buNNWii2IGroGakeoBnBipQ1V_ghmmFMRSk55Y_Rk5RWGGNVSXyEjqQktVBihjZf4QpiguLyOpSnuyZ2bWF8W1x4uGu_7VKGdSpyKJaQweZi2aUUbGdyF3wRXPElhgydL6d6O2D5-fjQn_kM0dgRT0_RI2f6BM-mOkffP364PDktzy8-nZ0cn5e2oiyXAsvG1FJU0trGgWOcWWBQD1cDcIa5dUpRaHnbOMoqV2PMMXWSW1rXTjRsjt7v5262zRpaCz5H0-tN7NYm7nQwnb6v-O6n_hGuNJNMksH-ZrLH8GsLKet1lyz0vfEQtkkLyZioGP0vSKpaVHjIao5e_wWuwjb64Q80xYQRJtT4LN5DNoaUIrjDwgTrMXE9Jq4V00Tp28QHy8s_Dz0YpogH_dWkj8479f6Et_8mtNv2fYabPKAv9ugq5RAPLMdMUvYbjFDKEA</recordid><startdate>19960917</startdate><enddate>19960917</enddate><creator>Vidal, Marc</creator><creator>Brachmann, Rainer K.</creator><creator>Fattaey, Ali</creator><creator>Harlow, Ed</creator><creator>Boeke, Jef D.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19960917</creationdate><title>Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions</title><author>Vidal, Marc ; Brachmann, Rainer K. ; Fattaey, Ali ; Harlow, Ed ; Boeke, Jef D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-708ba68758ccbfef343ce3e6107ee4304cf992ed4dbf235f600402f84c266f7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Alleles</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Blotting, Western</topic><topic>Consensus Sequence</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Primers</topic><topic>DNA, Fungal - metabolism</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Drug interactions</topic><topic>Fungal Proteins - biosynthesis</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>Genes, Reporter</topic><topic>Genetic mutation</topic><topic>Genetics</topic><topic>Medical genetics</topic><topic>Models, Genetic</topic><topic>Molecular Sequence Data</topic><topic>Molecules</topic><topic>Mutation</topic><topic>Phenotypes</topic><topic>Plasmids</topic><topic>Polymerase Chain Reaction</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Multimerization</topic><topic>Proteins</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Reporter genes</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - growth & development</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Transcription Factors</topic><topic>Two-Hybrid System Techniques</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vidal, Marc</creatorcontrib><creatorcontrib>Brachmann, Rainer K.</creatorcontrib><creatorcontrib>Fattaey, Ali</creatorcontrib><creatorcontrib>Harlow, Ed</creatorcontrib><creatorcontrib>Boeke, Jef D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vidal, Marc</au><au>Brachmann, Rainer K.</au><au>Fattaey, Ali</au><au>Harlow, Ed</au><au>Boeke, Jef D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1996-09-17</date><risdate>1996</risdate><volume>93</volume><issue>19</issue><spage>10315</spage><epage>10320</epage><pages>10315-10320</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Macromolecular interactions define many biological phenomena. Although genetic methods are available to identify novel protein-protein and DNA-protein interactions, no genetic system has thus far been described to identify molecules or mutations that dissociate known interactions. Herein, we describe genetic systems that detect such events in the yeast Saccharomyces cerevisiae. We have engineered yeast strains in which the interaction of two proteins expressed in the context of the two-hybrid system or the interaction between a DNA-binding protein and its binding site in the context of the one-hybrid system is deleterious to growth. Under these conditions, dissociation of the interaction provides a selective growth advantage, thereby facilitating detection. These methods referred to as the ``reverse two-hybrid system'' and ``reverse one-hybrid system'' facilitate the study of the structure-function relationships and regulation of protein-protein and DNA-protein interactions. They should also facilitate the selection of dissociator molecules that could be used as therapeutic agents.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8816797</pmid><doi>10.1073/pnas.93.19.10315</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Alleles Base Sequence Binding Sites Blotting, Western Consensus Sequence Deoxyribonucleic acid DNA DNA Primers DNA, Fungal - metabolism DNA-Binding Proteins - metabolism Drug interactions Fungal Proteins - biosynthesis Fungal Proteins - genetics Fungal Proteins - metabolism Genes, Reporter Genetic mutation Genetics Medical genetics Models, Genetic Molecular Sequence Data Molecules Mutation Phenotypes Plasmids Polymerase Chain Reaction Promoter Regions, Genetic Protein Multimerization Proteins Recombinant Proteins - biosynthesis Reporter genes Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - growth & development Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins Transcription Factors Two-Hybrid System Techniques Yeast Yeasts |
title | Reverse Two-Hybrid and One-Hybrid Systems to Detect Dissociation of Protein-Protein and DNA-Protein Interactions |
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