Generation of novel conditional and hypomorphic alleles of the Smad2 gene
Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFβ) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and...
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creator | Liu, Ye Festing, Maria H. Hester, Mark Thompson, John C. Weinstein, Michael |
description | Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFβ) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre‐loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2flox, was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre‐mediated recombination results in a deletion allele which phenocopies our previously reported Smad2ΔC null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad23loxP) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state. genesis 40:118–123, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/gene.20072 |
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It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre‐loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2flox, was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre‐mediated recombination results in a deletion allele which phenocopies our previously reported Smad2ΔC null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad23loxP) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state. genesis 40:118–123, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 1526-954X</identifier><identifier>EISSN: 1526-968X</identifier><identifier>DOI: 10.1002/gene.20072</identifier><identifier>PMID: 15452874</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Alleles ; Amino Acid Substitution ; Animals ; beta-Galactosidase - metabolism ; Blotting, Western ; Chromosome Mapping ; Cloning, Molecular ; conditional ; Cre ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Embryo, Mammalian - cytology ; Embryo, Mammalian - metabolism ; Embryo, Nonmammalian ; Embryonic Development ; Epitopes ; Exons ; Gene Deletion ; Gene Targeting ; Genetic Engineering - methods ; Genetic Vectors ; Homozygote ; hypomorph ; Integrases ; Introns ; loxP ; Mice ; Microinjections ; Mosaicism ; mouse ; Mutation ; null ; Polymerase Chain Reaction ; Recombination, Genetic ; Smad2 ; Smad2 Protein ; Stem Cells ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Viral Proteins ; Xenopus ; Xenopus Proteins</subject><ispartof>Genesis (New York, N.Y. : 2000), 2004-10, Vol.40 (2), p.118-123</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3752-ab9c801322baed7980e6c019842b92c6e12a8710eec2827da74d27a3112d7d3f3</citedby><cites>FETCH-LOGICAL-c3752-ab9c801322baed7980e6c019842b92c6e12a8710eec2827da74d27a3112d7d3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fgene.20072$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fgene.20072$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15452874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Ye</creatorcontrib><creatorcontrib>Festing, Maria H.</creatorcontrib><creatorcontrib>Hester, Mark</creatorcontrib><creatorcontrib>Thompson, John C.</creatorcontrib><creatorcontrib>Weinstein, Michael</creatorcontrib><title>Generation of novel conditional and hypomorphic alleles of the Smad2 gene</title><title>Genesis (New York, N.Y. : 2000)</title><addtitle>Genesis</addtitle><description>Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFβ) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre‐loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2flox, was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre‐mediated recombination results in a deletion allele which phenocopies our previously reported Smad2ΔC null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad23loxP) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state. genesis 40:118–123, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Alleles</subject><subject>Amino Acid Substitution</subject><subject>Animals</subject><subject>beta-Galactosidase - metabolism</subject><subject>Blotting, Western</subject><subject>Chromosome Mapping</subject><subject>Cloning, Molecular</subject><subject>conditional</subject><subject>Cre</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Embryo, Mammalian - cytology</subject><subject>Embryo, Mammalian - metabolism</subject><subject>Embryo, Nonmammalian</subject><subject>Embryonic Development</subject><subject>Epitopes</subject><subject>Exons</subject><subject>Gene Deletion</subject><subject>Gene Targeting</subject><subject>Genetic Engineering - methods</subject><subject>Genetic Vectors</subject><subject>Homozygote</subject><subject>hypomorph</subject><subject>Integrases</subject><subject>Introns</subject><subject>loxP</subject><subject>Mice</subject><subject>Microinjections</subject><subject>Mosaicism</subject><subject>mouse</subject><subject>Mutation</subject><subject>null</subject><subject>Polymerase Chain Reaction</subject><subject>Recombination, Genetic</subject><subject>Smad2</subject><subject>Smad2 Protein</subject><subject>Stem Cells</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Viral Proteins</subject><subject>Xenopus</subject><subject>Xenopus Proteins</subject><issn>1526-954X</issn><issn>1526-968X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhi1UBCHlwg9Ae-oBaak9u-uPYxWFJYhCpVLBzXLsCVnwrsM6acm_Z5cEuNGTR9bzPpp5CTli9JRRCt_vscFToFTADhmwAniquLz78jYX-d0-OYjxgVJaSIA9ss-KvAAp8gGZlF24NcsqNEmYJU34iz6xoXFV_2V8YhqXzNeLUId2Ma9sYrxHj7GHl3NMftfGQdJv8JXszoyPeLh9h-TP2fhmdJ5eXpeT0Y_L1GaigNRMlZWUZQBTg04oSZFbypTMYarAcmRgpGAU0YIE4YzIHQiTMQZOuGyWDcm3jXfRhqcVxqWuq2jRe9NgWEXNuWIFZ-q_IFNKgaJZB55sQNuGGFuc6UVb1aZda0Z137Du79OvDXfw8da6mtboPtBtpR3ANsC_yuP6E5Uux1fjN2m6yVRxic_vGdM-ai662vTtVakvcvlL8fKnvsleAM-ZlDw</recordid><startdate>200410</startdate><enddate>200410</enddate><creator>Liu, Ye</creator><creator>Festing, Maria H.</creator><creator>Hester, Mark</creator><creator>Thompson, John C.</creator><creator>Weinstein, Michael</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>200410</creationdate><title>Generation of novel conditional and hypomorphic alleles of the Smad2 gene</title><author>Liu, Ye ; Festing, Maria H. ; Hester, Mark ; Thompson, John C. ; Weinstein, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3752-ab9c801322baed7980e6c019842b92c6e12a8710eec2827da74d27a3112d7d3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Alleles</topic><topic>Amino Acid Substitution</topic><topic>Animals</topic><topic>beta-Galactosidase - metabolism</topic><topic>Blotting, Western</topic><topic>Chromosome Mapping</topic><topic>Cloning, Molecular</topic><topic>conditional</topic><topic>Cre</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Embryo, Mammalian - cytology</topic><topic>Embryo, Mammalian - metabolism</topic><topic>Embryo, Nonmammalian</topic><topic>Embryonic Development</topic><topic>Epitopes</topic><topic>Exons</topic><topic>Gene Deletion</topic><topic>Gene Targeting</topic><topic>Genetic Engineering - methods</topic><topic>Genetic Vectors</topic><topic>Homozygote</topic><topic>hypomorph</topic><topic>Integrases</topic><topic>Introns</topic><topic>loxP</topic><topic>Mice</topic><topic>Microinjections</topic><topic>Mosaicism</topic><topic>mouse</topic><topic>Mutation</topic><topic>null</topic><topic>Polymerase Chain Reaction</topic><topic>Recombination, Genetic</topic><topic>Smad2</topic><topic>Smad2 Protein</topic><topic>Stem Cells</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Viral Proteins</topic><topic>Xenopus</topic><topic>Xenopus Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Ye</creatorcontrib><creatorcontrib>Festing, Maria H.</creatorcontrib><creatorcontrib>Hester, Mark</creatorcontrib><creatorcontrib>Thompson, John C.</creatorcontrib><creatorcontrib>Weinstein, Michael</creatorcontrib><collection>Istex</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><jtitle>Genesis (New York, N.Y. : 2000)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Ye</au><au>Festing, Maria H.</au><au>Hester, Mark</au><au>Thompson, John C.</au><au>Weinstein, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of novel conditional and hypomorphic alleles of the Smad2 gene</atitle><jtitle>Genesis (New York, N.Y. : 2000)</jtitle><addtitle>Genesis</addtitle><date>2004-10</date><risdate>2004</risdate><volume>40</volume><issue>2</issue><spage>118</spage><epage>123</epage><pages>118-123</pages><issn>1526-954X</issn><eissn>1526-968X</eissn><abstract>Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFβ) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre‐loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2flox, was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre‐mediated recombination results in a deletion allele which phenocopies our previously reported Smad2ΔC null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad23loxP) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state. genesis 40:118–123, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15452874</pmid><doi>10.1002/gene.20072</doi><tpages>6</tpages></addata></record> |
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subjects | Alleles Amino Acid Substitution Animals beta-Galactosidase - metabolism Blotting, Western Chromosome Mapping Cloning, Molecular conditional Cre DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Embryo, Mammalian - cytology Embryo, Mammalian - metabolism Embryo, Nonmammalian Embryonic Development Epitopes Exons Gene Deletion Gene Targeting Genetic Engineering - methods Genetic Vectors Homozygote hypomorph Integrases Introns loxP Mice Microinjections Mosaicism mouse Mutation null Polymerase Chain Reaction Recombination, Genetic Smad2 Smad2 Protein Stem Cells Trans-Activators - genetics Trans-Activators - metabolism Viral Proteins Xenopus Xenopus Proteins |
title | Generation of novel conditional and hypomorphic alleles of the Smad2 gene |
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