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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Veröffentlicht in:Genesis (New York, N.Y. : 2000) N.Y. : 2000), 2004-10, Vol.40 (2), p.118-123
Hauptverfasser: Liu, Ye, Festing, Maria H., Hester, Mark, Thompson, John C., Weinstein, Michael
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container_end_page 123
container_issue 2
container_start_page 118
container_title Genesis (New York, N.Y. : 2000)
container_volume 40
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. 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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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