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Establishment of Smad2 conditional gene targeting mice based on the Cre-LoxP system

Establishment of Smad2 conditional gene targeting mice based on the Cre-LoxP system
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摘要 Smads is a new gene family in transforming growth factor-β(TGF-β) signaling pathway. Smad2 mutated in multiple human tumors and may be a candidate tumor suppressor gene. Targeted disruption of murine Smad2 gene resulted in embryonic lethality at E6.5. To study the function of Smad2 in vertebrate organgenesis and tumorigenesis, we constructed the Smad2 conditional targeting vector in which two LoxP sequences were placed to flank the sequences encoding the C terminal functional domain of Smad2. The validity of the LoxP sites in the targeting construct was tested in E. coli that express the Cre recombinase constitutively. The vector was electroporated into ES cells and 3 targeted ES cell clones were obtained by Southern blot screening. Targeted ES cells were introduced into C57BL/6J blastocysts by microinjection to generate germ-line chimeras. Genotyping analysis showed that 2 progeny among these chimeras carried the Smad2 conditional targeted allele. The establishment of Smad2 conditional gene targeting mouse has laid a solid foundation for producing the tissue specific Smad2 gene knockout mice. Smads is a new gene family in transforming growth factor-@ (TGF- @) signaling pathway. Smad2 mutated in multiple human tumors and may be a candidate tumor suppressor gene. Targeted disruption of murine Smad2 gene resulted in embryonic lethality at E6.5. To study the function of Smad2 in vertebrate organgenesis and tumorigenesis, we constructed the Smad2 conditional targeting vector in which two LoxP sequences were placed to flank the sequences encoding the C terminal functional domain of Smad2. The validity of the LoxP sites in the targeting construct was tested in E. coli that express the Cre recombinase constitutively. The vector was electropo-rated into ES cells and 3 targeted ES cell clones were obtained by Southern blot screening. Targeted ES cells were introduced into C57BL/6J blastocysts by microinjection to generate germ-line chimeras. Genotyping analysis showed that 2 progeny among these chimeras carried the Smad2 conditional targeted allele. The establishment of Smad2 conditional gene targeting mouse has laid a solid foundation for producing the tissue specific Smad2 gene knockout mice.
出处 《Science China(Life Sciences)》 SCIE CAS 2002年第2期129-137,共10页 中国科学(生命科学英文版)
基金 This work was supported by Hi-Tech Research and Development Program of China (102-08-08-02 ) National Science Fund for Distinguished Young Scholars ( 30025028 ).
关键词 Smad2 EMBRYONIC stem cell CRE-LOXP system CONDITIONAL gene knockout. Smad2, embryonic stem cell, Cre-LoxP system, conditional gene knockout.
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  • 1Stewart. C. L.Production of chimeras between embryonic stem cells and embryos, Meth[].Enzymol.1994

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