Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island
A sensitive, ubiquitously expressed tetracycline inducible system would be a valuable tool in mouse transgenesis. However, this has been difficult to obtain due to position effects observed at different chromosomal sites of transgene integration, which negatively affect expression in many tissues. T...
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description | A sensitive, ubiquitously expressed tetracycline inducible system would be a valuable tool in mouse transgenesis. However, this has been difficult to obtain due to position effects observed at different chromosomal sites of transgene integration, which negatively affect expression in many tissues. The aim of this study was to test the utility of a mammalian methylation-free CpG island to drive ubiquitous expression of the sensitive doxycycline (Dox) inducible rtTA2S-M2 Tet-transactivator in transgenic mice.
An 8 kb genomic fragment from the methylation-free CpG island of the human hnRNPA2B1-CBX3 housekeeping gene locus was tested. In a number of transgenic mouse lines obtained, rtTA2S-M2 expression was detected in many tissues examined. Characterisation of the highest expressing rtTA2S-M2 transgenic mouse line demonstrated Dox-inducible GFP transgene expression in many tissues. Using this line we also show highly sensitive quantitative induction with low doses of Dox of an assayable plasma protein transgene under the control of a Tet Responsive Element (TRE). The utility of this rtTA2S-M2 line for inducible expression in mouse embryos was also demonstrated using a GATA-6 Tet-inducible transgene to show specific phenotypes in the embryonic lung, as well as broader effects resulting from the inducible widespread overexpression of the transgene.
The ubiquitously expressing rtTA2S-M2 transgenic mouse line described here provides a very useful tool for studying the effects of the widespread, inducible overexpression of genes during embryonic development and in adult mice. |
doi_str_mv | 10.1186/1471-213x-7-108 |
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An 8 kb genomic fragment from the methylation-free CpG island of the human hnRNPA2B1-CBX3 housekeeping gene locus was tested. In a number of transgenic mouse lines obtained, rtTA2S-M2 expression was detected in many tissues examined. Characterisation of the highest expressing rtTA2S-M2 transgenic mouse line demonstrated Dox-inducible GFP transgene expression in many tissues. Using this line we also show highly sensitive quantitative induction with low doses of Dox of an assayable plasma protein transgene under the control of a Tet Responsive Element (TRE). The utility of this rtTA2S-M2 line for inducible expression in mouse embryos was also demonstrated using a GATA-6 Tet-inducible transgene to show specific phenotypes in the embryonic lung, as well as broader effects resulting from the inducible widespread overexpression of the transgene.
The ubiquitously expressing rtTA2S-M2 transgenic mouse line described here provides a very useful tool for studying the effects of the widespread, inducible overexpression of genes during embryonic development and in adult mice.</description><identifier>ISSN: 1471-213X</identifier><identifier>EISSN: 1471-213X</identifier><identifier>DOI: 10.1186/1471-213x-7-108</identifier><identifier>PMID: 17900353</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Animals ; Blotting, Northern ; CpG Islands - genetics ; DNA binding proteins ; Doxycycline ; Doxycycline - pharmacology ; Evaluation ; Gene Expression ; Genetic aspects ; Genetic engineering ; Genetically modified mice ; Green Fluorescent Proteins ; Growth ; Humans ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Insulator Elements - genetics ; Methodology ; Methods ; Mice ; Mice, Transgenic ; Phospholipid Transfer Proteins - genetics ; Physiological aspects ; Reverse Transcriptase Polymerase Chain Reaction ; Tissue Distribution ; Transgenes</subject><ispartof>BMC developmental biology, 2007-09, Vol.7 (1), p.108-108, Article 108</ispartof><rights>COPYRIGHT 2007 BioMed Central Ltd.</rights><rights>Copyright © 2007 Katsantoni et al; licensee BioMed Central Ltd. 2007 Katsantoni et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b648t-2144be4af2d24c0d89503da172912ea01d8fc6cdf0517f67aa91379a1d5980fe3</citedby><cites>FETCH-LOGICAL-b648t-2144be4af2d24c0d89503da172912ea01d8fc6cdf0517f67aa91379a1d5980fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2080639/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2080639/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,24801,27924,27925,53791,53793,75738,75739</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17900353$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katsantoni, Eleni Z</creatorcontrib><creatorcontrib>Anghelescu, Nora E</creatorcontrib><creatorcontrib>Rottier, Robbert</creatorcontrib><creatorcontrib>Moerland, Matthijs</creatorcontrib><creatorcontrib>Antoniou, Michael</creatorcontrib><creatorcontrib>de Crom, Rini</creatorcontrib><creatorcontrib>Grosveld, Frank</creatorcontrib><creatorcontrib>Strouboulis, John</creatorcontrib><title>Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island</title><title>BMC developmental biology</title><addtitle>BMC Dev Biol</addtitle><description>A sensitive, ubiquitously expressed tetracycline inducible system would be a valuable tool in mouse transgenesis. However, this has been difficult to obtain due to position effects observed at different chromosomal sites of transgene integration, which negatively affect expression in many tissues. The aim of this study was to test the utility of a mammalian methylation-free CpG island to drive ubiquitous expression of the sensitive doxycycline (Dox) inducible rtTA2S-M2 Tet-transactivator in transgenic mice.
An 8 kb genomic fragment from the methylation-free CpG island of the human hnRNPA2B1-CBX3 housekeeping gene locus was tested. In a number of transgenic mouse lines obtained, rtTA2S-M2 expression was detected in many tissues examined. Characterisation of the highest expressing rtTA2S-M2 transgenic mouse line demonstrated Dox-inducible GFP transgene expression in many tissues. Using this line we also show highly sensitive quantitative induction with low doses of Dox of an assayable plasma protein transgene under the control of a Tet Responsive Element (TRE). The utility of this rtTA2S-M2 line for inducible expression in mouse embryos was also demonstrated using a GATA-6 Tet-inducible transgene to show specific phenotypes in the embryonic lung, as well as broader effects resulting from the inducible widespread overexpression of the transgene.
The ubiquitously expressing rtTA2S-M2 transgenic mouse line described here provides a very useful tool for studying the effects of the widespread, inducible overexpression of genes during embryonic development and in adult mice.</description><subject>Animals</subject><subject>Blotting, Northern</subject><subject>CpG Islands - genetics</subject><subject>DNA binding proteins</subject><subject>Doxycycline</subject><subject>Doxycycline - pharmacology</subject><subject>Evaluation</subject><subject>Gene Expression</subject><subject>Genetic aspects</subject><subject>Genetic engineering</subject><subject>Genetically modified mice</subject><subject>Green Fluorescent Proteins</subject><subject>Growth</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Insulator Elements - genetics</subject><subject>Methodology</subject><subject>Methods</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Phospholipid Transfer Proteins - genetics</subject><subject>Physiological aspects</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tissue Distribution</subject><subject>Transgenes</subject><issn>1471-213X</issn><issn>1471-213X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1Uk1r3DAQNaWlSbc991YEhUAPzmosr2VfCrtLmwbSD_IBuQlZGu-q2NLGssPuv4-c3bYxpOggMfPm6c2biaL3QE8B8mwKKYc4AbaNeQw0fxEd_4ncvnzyPoreeP-bUuA5ZK-jI-AFpWzGjqPtTWnuetO53hPcblr03jhLXEW6NZK2u54nV_H3hBire2XKGonf-Q6bECBdK61foTWKNEYh0a25R0vK3WPtum-kJWt7-ePXPFnAdLm4ZWS5OSPG19Lqt9GrStYe3x3uSXTz9cv18lt88fPsfDm_iMsszbugPk1LTGWV6CRVVOfFjDItgScFJCgp6LxSmdIVnQGvMi5lAYwXEvSsyGmFbBJ93vNu-rJBrdAG2bXYtKaR7U44acQ4Y81arNy9SGhOM1YEgsWeoDTuPwTjjHKNGJwXg_OCizCXQHJyUNG6ux59JxrjFdbBCQzWh89YWrAwk0n0cQ9cyRqFsZULnGoAizlwSLMMYNB0-gwqHI1hEs5iZUJ8VPBpVBAwHW67ley9F-dXl2PsdI9VrfO-xepvr0DFsHXPdPfhqcf_8Ic1Yw8BDtGU</recordid><startdate>20070927</startdate><enddate>20070927</enddate><creator>Katsantoni, Eleni Z</creator><creator>Anghelescu, Nora E</creator><creator>Rottier, Robbert</creator><creator>Moerland, Matthijs</creator><creator>Antoniou, Michael</creator><creator>de Crom, Rini</creator><creator>Grosveld, Frank</creator><creator>Strouboulis, John</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>ISR</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20070927</creationdate><title>Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island</title><author>Katsantoni, Eleni Z ; Anghelescu, Nora E ; Rottier, Robbert ; Moerland, Matthijs ; Antoniou, Michael ; de Crom, Rini ; Grosveld, Frank ; Strouboulis, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b648t-2144be4af2d24c0d89503da172912ea01d8fc6cdf0517f67aa91379a1d5980fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Blotting, Northern</topic><topic>CpG Islands - genetics</topic><topic>DNA binding proteins</topic><topic>Doxycycline</topic><topic>Doxycycline - pharmacology</topic><topic>Evaluation</topic><topic>Gene Expression</topic><topic>Genetic aspects</topic><topic>Genetic engineering</topic><topic>Genetically modified mice</topic><topic>Green Fluorescent Proteins</topic><topic>Growth</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Insulator Elements - genetics</topic><topic>Methodology</topic><topic>Methods</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Phospholipid Transfer Proteins - genetics</topic><topic>Physiological aspects</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Tissue Distribution</topic><topic>Transgenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katsantoni, Eleni Z</creatorcontrib><creatorcontrib>Anghelescu, Nora E</creatorcontrib><creatorcontrib>Rottier, Robbert</creatorcontrib><creatorcontrib>Moerland, Matthijs</creatorcontrib><creatorcontrib>Antoniou, Michael</creatorcontrib><creatorcontrib>de Crom, Rini</creatorcontrib><creatorcontrib>Grosveld, Frank</creatorcontrib><creatorcontrib>Strouboulis, John</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katsantoni, Eleni Z</au><au>Anghelescu, Nora E</au><au>Rottier, Robbert</au><au>Moerland, Matthijs</au><au>Antoniou, Michael</au><au>de Crom, Rini</au><au>Grosveld, Frank</au><au>Strouboulis, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island</atitle><jtitle>BMC developmental biology</jtitle><addtitle>BMC Dev Biol</addtitle><date>2007-09-27</date><risdate>2007</risdate><volume>7</volume><issue>1</issue><spage>108</spage><epage>108</epage><pages>108-108</pages><artnum>108</artnum><issn>1471-213X</issn><eissn>1471-213X</eissn><abstract>A sensitive, ubiquitously expressed tetracycline inducible system would be a valuable tool in mouse transgenesis. However, this has been difficult to obtain due to position effects observed at different chromosomal sites of transgene integration, which negatively affect expression in many tissues. The aim of this study was to test the utility of a mammalian methylation-free CpG island to drive ubiquitous expression of the sensitive doxycycline (Dox) inducible rtTA2S-M2 Tet-transactivator in transgenic mice.
An 8 kb genomic fragment from the methylation-free CpG island of the human hnRNPA2B1-CBX3 housekeeping gene locus was tested. In a number of transgenic mouse lines obtained, rtTA2S-M2 expression was detected in many tissues examined. Characterisation of the highest expressing rtTA2S-M2 transgenic mouse line demonstrated Dox-inducible GFP transgene expression in many tissues. Using this line we also show highly sensitive quantitative induction with low doses of Dox of an assayable plasma protein transgene under the control of a Tet Responsive Element (TRE). The utility of this rtTA2S-M2 line for inducible expression in mouse embryos was also demonstrated using a GATA-6 Tet-inducible transgene to show specific phenotypes in the embryonic lung, as well as broader effects resulting from the inducible widespread overexpression of the transgene.
The ubiquitously expressing rtTA2S-M2 transgenic mouse line described here provides a very useful tool for studying the effects of the widespread, inducible overexpression of genes during embryonic development and in adult mice.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>17900353</pmid><doi>10.1186/1471-213x-7-108</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blotting, Northern CpG Islands - genetics DNA binding proteins Doxycycline Doxycycline - pharmacology Evaluation Gene Expression Genetic aspects Genetic engineering Genetically modified mice Green Fluorescent Proteins Growth Humans Immunohistochemistry In Situ Hybridization, Fluorescence Insulator Elements - genetics Methodology Methods Mice Mice, Transgenic Phospholipid Transfer Proteins - genetics Physiological aspects Reverse Transcriptase Polymerase Chain Reaction Tissue Distribution Transgenes |
title | Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island |
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