Differential Plasmid Rescue From Transgenic Mouse DNAs Into Escherichia coli Methylation-Restriction Mutants
Plasmids comprising transgene insertions in four lines of transgenic mice have been retrieved by plasmid rescue into a set of Escherichia coli strains with mutations in different members of the methylation-dependent restriction system (MDRS). Statistical analysis of plasmid rescue frequencies has re...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1990-06, Vol.87 (12), p.4645-4649 |
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creator | Seth G. N. Grant Jessee, Joel Bloom, Fredric R. Hanahan, Douglas |
description | Plasmids comprising transgene insertions in four lines of transgenic mice have been retrieved by plasmid rescue into a set of Escherichia coli strains with mutations in different members of the methylation-dependent restriction system (MDRS). Statistical analysis of plasmid rescue frequencies has revealed that the MDRS loci detect differential modifications of the transgene insertions among mouse lines that show distinctive patterns of transgene expression. Plasmids in mice that express hybrid insulin transgenes during development can be readily cloned into E. coli strains carrying mutations in two of the MDRS loci, mcrA and mcrB. In mice in which transgene expression is inappropriately delayed into adulthood, plasmids can only be cloned into E. coli that carry mutations in all known MDRS activities. Differential cloning frequencies in the presence or absence of the various methylation-dependent restriction genes represent a further way to distinguish regions of mammalian chromosomes. These multiply deficient E. coli strains will also facilitate the molecular cloning of modified chromosomal DNA. |
doi_str_mv | 10.1073/pnas.87.12.4645 |
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N. Grant ; Jessee, Joel ; Bloom, Fredric R. ; Hanahan, Douglas</creator><creatorcontrib>Seth G. N. Grant ; Jessee, Joel ; Bloom, Fredric R. ; Hanahan, Douglas</creatorcontrib><description>Plasmids comprising transgene insertions in four lines of transgenic mice have been retrieved by plasmid rescue into a set of Escherichia coli strains with mutations in different members of the methylation-dependent restriction system (MDRS). Statistical analysis of plasmid rescue frequencies has revealed that the MDRS loci detect differential modifications of the transgene insertions among mouse lines that show distinctive patterns of transgene expression. Plasmids in mice that express hybrid insulin transgenes during development can be readily cloned into E. coli strains carrying mutations in two of the MDRS loci, mcrA and mcrB. In mice in which transgene expression is inappropriately delayed into adulthood, plasmids can only be cloned into E. coli that carry mutations in all known MDRS activities. Differential cloning frequencies in the presence or absence of the various methylation-dependent restriction genes represent a further way to distinguish regions of mammalian chromosomes. These multiply deficient E. coli strains will also facilitate the molecular cloning of modified chromosomal DNA.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.87.12.4645</identifier><identifier>PMID: 2162051</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Biological and medical sciences ; Biotechnology ; Chromosome Mapping ; DNA ; DNA - genetics ; DNA Transposable Elements ; Enzymes ; Escherichia coli ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Genes ; Genetic engineering ; Genetic loci ; Genetic mutation ; Genetic technics ; Genotype ; Methods. Procedures. Technologies ; Methylation ; Mice ; Mice, Transgenic ; Mutation ; Plasmids ; Plasmids - genetics ; Restriction Mapping ; Transgenes ; Transgenic animals ; Transgenic animals and transgenic plants</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (12), p.4645-4649</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-994b8b44d258f433268ed62f7a1eb8c1e91f712314f2a6df1304c62dd1046b1d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/87/12.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2354378$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2354378$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,724,777,781,800,882,27905,27906,53772,53774,57998,58231</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19508608$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2162051$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seth G. N. Grant</creatorcontrib><creatorcontrib>Jessee, Joel</creatorcontrib><creatorcontrib>Bloom, Fredric R.</creatorcontrib><creatorcontrib>Hanahan, Douglas</creatorcontrib><title>Differential Plasmid Rescue From Transgenic Mouse DNAs Into Escherichia coli Methylation-Restriction Mutants</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Plasmids comprising transgene insertions in four lines of transgenic mice have been retrieved by plasmid rescue into a set of Escherichia coli strains with mutations in different members of the methylation-dependent restriction system (MDRS). Statistical analysis of plasmid rescue frequencies has revealed that the MDRS loci detect differential modifications of the transgene insertions among mouse lines that show distinctive patterns of transgene expression. Plasmids in mice that express hybrid insulin transgenes during development can be readily cloned into E. coli strains carrying mutations in two of the MDRS loci, mcrA and mcrB. In mice in which transgene expression is inappropriately delayed into adulthood, plasmids can only be cloned into E. coli that carry mutations in all known MDRS activities. Differential cloning frequencies in the presence or absence of the various methylation-dependent restriction genes represent a further way to distinguish regions of mammalian chromosomes. These multiply deficient E. coli strains will also facilitate the molecular cloning of modified chromosomal DNA.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Chromosome Mapping</subject><subject>DNA</subject><subject>DNA - genetics</subject><subject>DNA Transposable Elements</subject><subject>Enzymes</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genetic engineering</subject><subject>Genetic loci</subject><subject>Genetic mutation</subject><subject>Genetic technics</subject><subject>Genotype</subject><subject>Methods. Procedures. Technologies</subject><subject>Methylation</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mutation</subject><subject>Plasmids</subject><subject>Plasmids - genetics</subject><subject>Restriction Mapping</subject><subject>Transgenes</subject><subject>Transgenic animals</subject><subject>Transgenic animals and transgenic plants</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhSMEKkNhzQaQN8AqUz9jR2JT9QGVOoBQWVuOY3dcOfFgO4j-exxNaOkGVrZ0vvs491TVSwTXCHJytBtVWgu-RnhNG8oeVSsEW1Q3tIWPqxWEmNeCYvq0epbSDYSwZQIeVAcYNRgytKr8qbPWRDNmpzz46lUaXA--maQnA85jGMBVVGO6NqPTYBOmZMDp5-MELsYcwFnSWxOd3joFdPAObEze3nqVXRjr0iMXbf6DzZTVmNPz6olVPpkXy3tYfT8_uzr5VF9--XhxcnxZa4ZJrtuWdqKjtMdMWEoIboTpG2y5QqYTGpkWWY4wQdRi1fQWEUh1g_seQdp0qCeH1Yd9393UDabXxV1UXu6iG1S8lUE5-VAZ3VZeh5-SUcRJKX-3lMfwYyo25OCSNt6r0ZQLSN4KLGAh_wcixhmmLS7g0R7UMaQUjb3bBUE55yjnHKXgEmE551gqXv9t4Y5fgiv620VXSStvS0japfu2LYOigaJwbxZuHvBHfjDo_T8BaSfvs_mVC_lqT96kHOL9RoRRwgX5DVeXyXU</recordid><startdate>19900601</startdate><enddate>19900601</enddate><creator>Seth G. N. Grant</creator><creator>Jessee, Joel</creator><creator>Bloom, Fredric R.</creator><creator>Hanahan, Douglas</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad 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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19900601</creationdate><title>Differential Plasmid Rescue From Transgenic Mouse DNAs Into Escherichia coli Methylation-Restriction Mutants</title><author>Seth G. N. Grant ; Jessee, Joel ; Bloom, Fredric R. ; Hanahan, Douglas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-994b8b44d258f433268ed62f7a1eb8c1e91f712314f2a6df1304c62dd1046b1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Chromosome Mapping</topic><topic>DNA</topic><topic>DNA - genetics</topic><topic>DNA Transposable Elements</topic><topic>Enzymes</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genetic engineering</topic><topic>Genetic loci</topic><topic>Genetic mutation</topic><topic>Genetic technics</topic><topic>Genotype</topic><topic>Methods. Procedures. Technologies</topic><topic>Methylation</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mutation</topic><topic>Plasmids</topic><topic>Plasmids - genetics</topic><topic>Restriction Mapping</topic><topic>Transgenes</topic><topic>Transgenic animals</topic><topic>Transgenic animals and transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seth G. N. Grant</creatorcontrib><creatorcontrib>Jessee, Joel</creatorcontrib><creatorcontrib>Bloom, Fredric R.</creatorcontrib><creatorcontrib>Hanahan, Douglas</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>Technology Research Database</collection><collection>Engineering Research Database</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>Seth G. N. Grant</au><au>Jessee, Joel</au><au>Bloom, Fredric R.</au><au>Hanahan, Douglas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Plasmid Rescue From Transgenic Mouse DNAs Into Escherichia coli Methylation-Restriction Mutants</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1990-06-01</date><risdate>1990</risdate><volume>87</volume><issue>12</issue><spage>4645</spage><epage>4649</epage><pages>4645-4649</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>Plasmids comprising transgene insertions in four lines of transgenic mice have been retrieved by plasmid rescue into a set of Escherichia coli strains with mutations in different members of the methylation-dependent restriction system (MDRS). Statistical analysis of plasmid rescue frequencies has revealed that the MDRS loci detect differential modifications of the transgene insertions among mouse lines that show distinctive patterns of transgene expression. Plasmids in mice that express hybrid insulin transgenes during development can be readily cloned into E. coli strains carrying mutations in two of the MDRS loci, mcrA and mcrB. In mice in which transgene expression is inappropriately delayed into adulthood, plasmids can only be cloned into E. coli that carry mutations in all known MDRS activities. Differential cloning frequencies in the presence or absence of the various methylation-dependent restriction genes represent a further way to distinguish regions of mammalian chromosomes. These multiply deficient E. coli strains will also facilitate the molecular cloning of modified chromosomal DNA.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>2162051</pmid><doi>10.1073/pnas.87.12.4645</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Biotechnology Chromosome Mapping DNA DNA - genetics DNA Transposable Elements Enzymes Escherichia coli Escherichia coli - genetics Fundamental and applied biological sciences. Psychology Genes Genetic engineering Genetic loci Genetic mutation Genetic technics Genotype Methods. Procedures. Technologies Methylation Mice Mice, Transgenic Mutation Plasmids Plasmids - genetics Restriction Mapping Transgenes Transgenic animals Transgenic animals and transgenic plants |
title | Differential Plasmid Rescue From Transgenic Mouse DNAs Into Escherichia coli Methylation-Restriction Mutants |
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