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公开(公告)号:EP2262898B1
公开(公告)日:2018-01-24
申请号:EP09718915.3
申请日:2009-03-06
发明人: POUEYMIROU, William , DECHIARA, Thomas, M. , AUERBACH, Wojtek , ECONOMIDES, Aris, N. , GALE, Nicholas, W. , FRENDEWEY, David , VALENZUELA,David, M.
CPC分类号: A01K67/0271 , A01K67/0275 , A01K2207/12 , A01K2217/00 , A01K2217/05 , A01K2217/07 , A01K2217/15 , A01K2217/203 , A01K2217/30 , A01K2227/105 , A01K2267/02 , C12N5/16 , C12N15/8509 , C12N15/907 , C12N2510/00 , C12N2517/02
摘要: Genetically modified mice and nucleic acid constructs for making the genetically modified mice are described. A first mouse having a gene encoding an activator (such as a Cre recombinase) operably linked to a developmentally-regulated promoter (such as a Nanog promoter) is provided. A second mouse having a toxic responder gene (such as a gene encoding diphtheria toxin A) is provided, where the toxic gene is expressed only in the presence of an activator, Embryos from a mating of the first and the second mouse are provided as host embryos suitable for generating mice from donor cells introduced into the host embryos. Ablating the ICM of a mouse embryo physically, chemically, or genetically is described, as well as making F0 generation mice that are substantially or in full derived from donor cells, employing a host mouse embryo with an ablated or nonproliferating ICM.
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公开(公告)号:EP2262898A1
公开(公告)日:2010-12-22
申请号:EP09718915.3
申请日:2009-03-06
发明人: POUEYMIROU, William , DECHIARA, Thomas, M. , AUERBACH, Wojtek , ECONOMIDES, Aris, N. , GALE, Nicholas, W. , FRENDEWEY, David , VALENZUELA,David, M.
CPC分类号: A01K67/0271 , A01K67/0275 , A01K2207/12 , A01K2217/00 , A01K2217/05 , A01K2217/07 , A01K2217/15 , A01K2217/203 , A01K2217/30 , A01K2227/105 , A01K2267/02 , C12N5/16 , C12N15/8509 , C12N15/907 , C12N2510/00 , C12N2517/02
摘要: Genetically modified mice and nucleic acid constructs for making the genetically modified mice are described. A first mouse having a gene encoding an activator (such as a Cre recombinase) operably linked to a developmentally-regulated promoter (such as a Nanog promoter) is provided. A second mouse having a toxic responder gene (such as a gene encoding diphtheria toxin A) is provided, where the toxic gene is expressed only in the presence of an activator, Embryos from a mating of the first and the second mouse are provided as host embryos suitable for generating mice from donor cells introduced into the host embryos. Ablating the ICM of a mouse embryo physically, chemically, or genetically is described, as well as making F0 generation mice that are substantially or in full derived from donor cells, employing a host mouse embryo with an ablated or nonproliferating ICM.
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