Wintermantel Tim M, Mayer Anja K, Schütz Günther, Greiner Erich F
Division Molecular Biology of the Cell I, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Genesis. 2002 Jul;33(3):125-30. doi: 10.1002/gene.10097.
We describe the generation of transgenic mouse lines expressing Cre recombinase in epithelial cells of the lactating mammary gland. As an expression vector, we used a P1-derived bacterial artificial chromosome (PAC) which harbors the gene for the secretory milk protein, whey acidic protein (Wap). Using homologous recombination in E. coli, the PAC was modified to carry the improved coding sequence of Cre recombinase (iCre). Transgenic lines carrying the WAPiCre PAC express Cre recombinase efficiently in the majority of mammary epithelial cells upon lactation. Of only four transgenic lines produced, three express Cre recombinase to a high efficiency. LoxP-flanked DNA sequences are recombined in virtually all epithelial cells of WAPiCre transgenic mice at lactation day 3.
我们描述了在哺乳期乳腺上皮细胞中表达Cre重组酶的转基因小鼠品系的产生。作为表达载体,我们使用了一种源自P1的细菌人工染色体(PAC),其携带分泌性乳蛋白乳清酸性蛋白(Wap)的基因。通过在大肠杆菌中进行同源重组,对PAC进行修饰以携带改进的Cre重组酶编码序列(iCre)。携带WAPiCre PAC的转基因品系在哺乳期时在大多数乳腺上皮细胞中高效表达Cre重组酶。在仅产生的四个转基因品系中,有三个高效表达Cre重组酶。在哺乳期第3天,loxP侧翼的DNA序列在WAPiCre转基因小鼠的几乎所有上皮细胞中发生重组。