Selfridge J, Pow A M, McWhir J, Magin T M, Melton D W
Institute of Cell and Molecular Biology, University of Edinburgh, Scotland.
Somat Cell Mol Genet. 1992 Jul;18(4):325-36. doi: 10.1007/BF01235756.
A convenient system for gene targeting that uses hypoxanthine phosphoribosyltransferase (HPRT) minigenes as the selectable marker in HPRT-deficient mouse embryonic stem (ES) cells is described. Improvements to the expression of HPRT minigenes in ES cells were achieved by promoter substitution and the provision of a strong translational initiation signal. The use of minigenes in the positive-negative selection strategy for gene targeting was evaluated and the smaller minigenes were found to be as effective as a more conventional marker--the herpes simplex virus thymidine kinase gene. Minigenes were used to target the DNA repair gene ERCC-1 in ES cells. A new HPRT-deficient ES cell line was developed that contributes with high frequency to the germ line of chimeric animals. The ability to select for and against HPRT minigene expression in the new HPRT-deficient ES cell line will make this system useful for a range of gene-targeting applications.
描述了一种便捷的基因靶向系统,该系统在缺乏次黄嘌呤磷酸核糖基转移酶(HPRT)的小鼠胚胎干细胞(ES细胞)中使用HPRT小基因作为选择标记。通过启动子替换和提供强翻译起始信号,实现了ES细胞中HPRT小基因表达的改善。评估了小基因在基因靶向的正负选择策略中的应用,发现较小的小基因与更传统的标记——单纯疱疹病毒胸苷激酶基因一样有效。小基因用于靶向ES细胞中的DNA修复基因ERCC-1。开发了一种新的缺乏HPRT的ES细胞系,该细胞系能以高频率参与嵌合动物的生殖系。在新的缺乏HPRT的ES细胞系中选择和反选HPRT小基因表达的能力将使该系统适用于一系列基因靶向应用。