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Targeted integration of neomycin into yeast artificial chromosomes (YACs) for transfection into mammalian cells.

机译:将新霉素靶向整合到酵母人工染色体(YAC)中,以转染到哺乳动物细胞中。

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摘要

Vectors have been constructed for the introduction of the neomycin resistance gene (neo) into the left arm, right arm or human insert DNA of yeast artificial chromosomes (YACs) by homologous recombination. These vectors contain a yeast selectable marker Lys-2, i.e. the alpha-aminoadipidate reductase gene, and a mammalian selection marker, neo, which confers G418 resistance. The vectors can be used to modify YACs in the most commonly used yeast strain for YAC library construction, AB1380. Specific targeting can be carried out by transfection of restriction endonuclease treated linear plasmids, with highly specific recombinogenic ends, into the YAC containing yeast cells. Analysis of targeted YACs confirmed that all three vectors can target correctly in yeast. Introduction of one of the targeted YACs into V79 (Chinese hamster fibroblast) cells showed complete and intact transfer of the YAC.
机译:已经构建了通过同源重组将新霉素抗性基因(neo)引入酵母人工染色体(YAC)的左臂,右臂或人插入DNA的载体。这些载体包含酵母选择标记Lys-2,即α-氨基己二酸酯还原酶基因,和哺乳动物选择标记neo,其赋予G418抗性。载体可用于修饰最常用的酵母菌株中的YAC,用于YAC文库构建,AB1380。可以通过将限制性内切核酸酶处理的线性质粒(具有高度特异性的重组末端)转染到含YAC的酵母细胞中来进行特异性靶向。靶向YAC的分析证实,所有三种载体均可在酵母中正确靶向。将一种靶向的YAC导入V79(中国仓鼠成纤维细胞)细胞显示出YAC的完整转移。

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