Schedl A, Montoliu L, Kelsey G, Schütz G
Division Molecular Biology of the Cell I, German Cancer Research Center, Heidelberg.
Nature. 1993 Mar 18;362(6417):258-61. doi: 10.1038/362258a0.
Expression of transgenes in mice often fails to follow the normal temporal and spatial pattern and to reach the same level as the endogenous copies. Only in exceptional cases has position-independent and copy number-dependent expression been reproduced. The size constraint of standard constructs may prevent the inclusion of important remote regulatory elements. Yeast artificial chromosomes (YACs) provide a means of cloning large DNA fragments and the transfer of YAC DNA into somatic cells has been reported. We have previously produced transgenic mice carrying a 35 kilobase YAC construct. Here we report the transfer of a 250 kilobase YAC covering the mouse tyrosinase gene into mice by pronuclear injection of gel-purified YAC DNA. The YAC was inserted into the mouse genome without major rearrangements and expression of the YAC-borne tyrosinase gene resulted in complete rescue of the albino phenotype of the recipient mice. Expression from the transgene reached levels comparable to that of the endogenous gene and showed copy number dependence and position independence.
转基因在小鼠中的表达往往无法遵循正常的时空模式,也无法达到与内源基因相同的水平。只有在特殊情况下,才能重现位置独立和拷贝数依赖的表达。标准构建体的大小限制可能会妨碍重要的远程调控元件的纳入。酵母人工染色体(YAC)提供了一种克隆大片段DNA的方法,并且已有报道将YAC DNA转移到体细胞中。我们之前已经培育出携带35千碱基YAC构建体的转基因小鼠。在此,我们报告通过原核注射凝胶纯化的YAC DNA,将覆盖小鼠酪氨酸酶基因的250千碱基YAC转移到小鼠体内。YAC被插入到小鼠基因组中,没有发生重大重排,并且YAC携带的酪氨酸酶基因的表达完全拯救了受体小鼠的白化病表型。转基因的表达水平与内源基因相当,显示出拷贝数依赖性和位置独立性。