Transcription-Driven Site-Specific DNA Recombination in vitro
Transcription of a topologically relaxed, circular DNA triggers recombination between two directly repeated res sites by γδ resolvase in vitro. This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase track...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1993-04, Vol.90 (7), p.2759-2763 |
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description | Transcription of a topologically relaxed, circular DNA triggers recombination between two directly repeated res sites by γδ resolvase in vitro. This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase tracking. In addition to functioning as a site-specific recombinase, γδ resolvase acts as a site-specific topoisomerase and increases the topological linking number of templates during transcription. The data suggest that the link between transcription and recombination could be negative DNA supercoiling that transiently builds up on a relatively short DNA segment in the wake of an advancing RNA polymerase. Surprisingly, transcription-driven recombination is not inhibited by the presence of large amounts of eukaryotic topoisomerase type I, indicating that site-specific recombination can override relaxation by diffusible topoisomerases. This in vitro system might therefore serve as a model for some transcription-directed recombination events observed in vivo. |
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This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase tracking. In addition to functioning as a site-specific recombinase, γδ resolvase acts as a site-specific topoisomerase and increases the topological linking number of templates during transcription. The data suggest that the link between transcription and recombination could be negative DNA supercoiling that transiently builds up on a relatively short DNA segment in the wake of an advancing RNA polymerase. Surprisingly, transcription-driven recombination is not inhibited by the presence of large amounts of eukaryotic topoisomerase type I, indicating that site-specific recombination can override relaxation by diffusible topoisomerases. This in vitro system might therefore serve as a model for some transcription-directed recombination events observed in vivo.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.90.7.2759</identifier><identifier>PMID: 8385342</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Bacteria ; Bacteriophage T7 - enzymology ; Bacteriophage T7 - genetics ; Biochemistry ; Biological and medical sciences ; Bromides ; Cattle ; Cytidine Monophosphate - metabolism ; Deoxyribonucleic acid ; DNA ; DNA - genetics ; DNA Topoisomerases, Type I - metabolism ; DNA-Directed RNA Polymerases - genetics ; Electrophoresis ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Gels ; Genic rearrangement. Recombination. Transposable element ; Kinetics ; Molecular and cellular biology ; Molecular genetics ; Nucleic acids ; Nucleotidyltransferases - metabolism ; Phosphorus Radioisotopes ; Plasmids ; Promoter Regions, Genetic ; Recombination, Genetic ; Restriction Mapping ; Ribonucleic acid ; RNA ; Templates, Genetic ; Thymus Gland - enzymology ; Topology ; Transcription, Genetic ; Transposases</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1993-04, Vol.90 (7), p.2759-2763</ispartof><rights>Copyright 1993 The National Academy of Sciences of the United States of America</rights><rights>1993 INIST-CNRS</rights><rights>Copyright National Academy of Sciences Apr 1, 1993</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5549-7075dde83e6588eaf17ae037e04968532e2fdbe280a8cb17eda3635f727dc7583</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/90/7.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2361617$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2361617$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27923,27924,53790,53792,58016,58249</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4737159$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8385342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Droge, Peter</creatorcontrib><title>Transcription-Driven Site-Specific DNA Recombination in vitro</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Transcription of a topologically relaxed, circular DNA triggers recombination between two directly repeated res sites by γδ resolvase in vitro. This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase tracking. In addition to functioning as a site-specific recombinase, γδ resolvase acts as a site-specific topoisomerase and increases the topological linking number of templates during transcription. The data suggest that the link between transcription and recombination could be negative DNA supercoiling that transiently builds up on a relatively short DNA segment in the wake of an advancing RNA polymerase. Surprisingly, transcription-driven recombination is not inhibited by the presence of large amounts of eukaryotic topoisomerase type I, indicating that site-specific recombination can override relaxation by diffusible topoisomerases. This in vitro system might therefore serve as a model for some transcription-directed recombination events observed in vivo.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Bacteriophage T7 - enzymology</subject><subject>Bacteriophage T7 - genetics</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Bromides</subject><subject>Cattle</subject><subject>Cytidine Monophosphate - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - genetics</subject><subject>DNA Topoisomerases, Type I - metabolism</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>Electrophoresis</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Genic rearrangement. Recombination. Transposable element</subject><subject>Kinetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Nucleic acids</subject><subject>Nucleotidyltransferases - metabolism</subject><subject>Phosphorus Radioisotopes</subject><subject>Plasmids</subject><subject>Promoter Regions, Genetic</subject><subject>Recombination, Genetic</subject><subject>Restriction Mapping</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Templates, Genetic</subject><subject>Thymus Gland - enzymology</subject><subject>Topology</subject><subject>Transcription, Genetic</subject><subject>Transposases</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhYMoYzu6daXQiLirMs9KAroYZnzBoOCM65BO3dI01UmZVDX6703ZPcUogqu7ON-5r4PQY4JrgiV7OQSba41rWVMp9B20IliTquEa30UrjKmsFKf8PnqQ8xZjrIXCJ-hEMSUYpyv0-jrZkF3yw-hjqC6S30NYX_kRqqsBnO-8W198PFt_Bhd3Gx_sjK19WO_9mOJDdK-zfYZHx3qKvrx9c33-vrr89O7D-dll5YTgupJYirYFxaARSoHtiLSAmQTMdVMWoUC7dgNUYavchkhoLWuY6CSVrZNCsVP06tB3mDY7aB2EMdneDMnvbPppovXmTyX4b-Zr3BveECmK_cXRnuL3CfJodj476HsbIE7ZSNFwqrn6L0gaQWmDSQGf_QVu45RC-YGhmFCpuKYFqg-QSzHnBN2yMMFmDs_M4RmNjTRzeMXw9PaZC35Mq-jPj7rNzvZdic75vGBcMkl-t7m5Ym5_oy5jTDf1_Qg_xlvz_gkW_clB3-YxpgWgrCHlr-wXJczCvg</recordid><startdate>19930401</startdate><enddate>19930401</enddate><creator>Droge, Peter</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>IQODW</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>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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19930401</creationdate><title>Transcription-Driven Site-Specific DNA Recombination in vitro</title><author>Droge, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5549-7075dde83e6588eaf17ae037e04968532e2fdbe280a8cb17eda3635f727dc7583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Bacteria</topic><topic>Bacteriophage T7 - enzymology</topic><topic>Bacteriophage T7 - genetics</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>Bromides</topic><topic>Cattle</topic><topic>Cytidine Monophosphate - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - genetics</topic><topic>DNA Topoisomerases, Type I - metabolism</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>Electrophoresis</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Genic rearrangement. Recombination. Transposable element</topic><topic>Kinetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Nucleic acids</topic><topic>Nucleotidyltransferases - metabolism</topic><topic>Phosphorus Radioisotopes</topic><topic>Plasmids</topic><topic>Promoter Regions, Genetic</topic><topic>Recombination, Genetic</topic><topic>Restriction Mapping</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Templates, Genetic</topic><topic>Thymus Gland - enzymology</topic><topic>Topology</topic><topic>Transcription, Genetic</topic><topic>Transposases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Droge, Peter</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>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>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>Droge, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcription-Driven Site-Specific DNA Recombination in vitro</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1993-04-01</date><risdate>1993</risdate><volume>90</volume><issue>7</issue><spage>2759</spage><epage>2763</epage><pages>2759-2763</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>Transcription of a topologically relaxed, circular DNA triggers recombination between two directly repeated res sites by γδ resolvase in vitro. This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase tracking. In addition to functioning as a site-specific recombinase, γδ resolvase acts as a site-specific topoisomerase and increases the topological linking number of templates during transcription. The data suggest that the link between transcription and recombination could be negative DNA supercoiling that transiently builds up on a relatively short DNA segment in the wake of an advancing RNA polymerase. Surprisingly, transcription-driven recombination is not inhibited by the presence of large amounts of eukaryotic topoisomerase type I, indicating that site-specific recombination can override relaxation by diffusible topoisomerases. This in vitro system might therefore serve as a model for some transcription-directed recombination events observed in vivo.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8385342</pmid><doi>10.1073/pnas.90.7.2759</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bacteria Bacteriophage T7 - enzymology Bacteriophage T7 - genetics Biochemistry Biological and medical sciences Bromides Cattle Cytidine Monophosphate - metabolism Deoxyribonucleic acid DNA DNA - genetics DNA Topoisomerases, Type I - metabolism DNA-Directed RNA Polymerases - genetics Electrophoresis Enzymes Fundamental and applied biological sciences. Psychology Gels Genic rearrangement. Recombination. Transposable element Kinetics Molecular and cellular biology Molecular genetics Nucleic acids Nucleotidyltransferases - metabolism Phosphorus Radioisotopes Plasmids Promoter Regions, Genetic Recombination, Genetic Restriction Mapping Ribonucleic acid RNA Templates, Genetic Thymus Gland - enzymology Topology Transcription, Genetic Transposases |
title | Transcription-Driven Site-Specific DNA Recombination in vitro |
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