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Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells.

Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells. Research Abstract Details 

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  • Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells. Abstract Text:

    sanae hamanakaSanae Hamanaka,tsukasa nabekuraTsukasa Nabekura,makoto otsuMakoto Otsu,hisahiro yoshidaHisahiro Yoshida,michio nagataMichio Nagata,joichi usuiJoichi Usui,satoru takahashiSatoru Takahashi,toshiro nagasawaToshiro Nagasawa,hiromitsu nakauchiHiromitsu Nakauchi,masafumi onoderaMasafumi Onodera,sanae hamanakaSanae Hamanaka,tsukasa nabekuraTsukasa Nabekura,makoto otsuMakoto Otsu,hisahiro yoshidaHisahiro Yoshida,michio nagataMichio Nagata,joichi usuiJoichi Usui,satoru takahashiSatoru Takahashi,toshiro nagasawaToshiro Nagasawa,hiromitsu nakauchiHiromitsu Nakauchi,masafumi onoderaMasafumi Onodera,

    Silencing of transduced genes hampers production of transgenic mice using retroviral vectors. We show stable expression of the enhanced green fluorescent protein (EGFP) gene in chimeric mice generated from retrovirally transduced embryonic stem cells. The vector was a murine stem cell virus-typed retroviral vector (GCDsap) in which the long terminal repeat and primer-binding site were derived from a PCC4 cell-passaged myeloproliferative sarcoma virus and the endogenous retrovirus dl587rev, respectively. To increase the viral titer, the vector was packaged with vesicular stomatitis virus G protein, which allowed concentration of the virus into pellets followed by resuspension in serum-free medium. In chimeric mice, EGFP was detected in various tissues including hematopoietic cells, neurons, cardiac muscle, and intestine. Furthermore, high expression was maintained in the progeny of these mice, suggesting successful germline transmission of active proviruses. Although the proportion of EGFP-expressing cells and the mean intensity of EGFP expression varied among tissues and mice, 100% of peripheral blood leukocytes expressed EGFP in mice carrying a single provirus copy, as well as in their progeny. Therefore, the gene transfer system described here provides a useful tool not only to generate transgenic animals but also to manipulate human embryonic stem cells.Molecular Therapy (2007) 15, 560-565. doi:10.1038/sj.mt.6300063; published online 19 December 2006.

    Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells. Publishing Authors By Initials

    s hamanakaS Hamanaka,t nabekuraT Nabekura,m otsuM Otsu,h yoshidaH Yoshida,m nagataM Nagata,j usuiJ Usui,s takahashiS Takahashi,t nagasawaT Nagasawa,h nakauchiH Nakauchi,m onoderaM Onodera,s hamanakaS Hamanaka,t nabekuraT Nabekura,m otsuM Otsu,h yoshidaH Yoshida,m nagataM Nagata,j usuiJ Usui,s takahashiS Takahashi,t nagasawaT Nagasawa,h nakauchiH Nakauchi,m onoderaM Onodera,

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    Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Molecular therapy : the journal of the American So

    VOLUME: 15

    Page Numbers: 560-5

    Journal Abbreviation: Mol. Ther.

    ISSN: 1525-0016

    DAY: 19

    MONTH: 12

    YEAR: 2006

    Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells. Information

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    LANGUAGE: eng

    NlmUniqueID: 100890581

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    Grant and Affiliation Information for Stable transgene expression in mice generated from retrovirally transduced embryonic stem cells.

    AFFILIATION: 1Major of Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Mol Ther

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