Zhang H, Hasty P, Bradley A
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.
Mol Cell Biol. 1994 Apr;14(4):2404-10. doi: 10.1128/mcb.14.4.2404-2410.1994.
We analyzed the gene targeting frequencies and recombination products generated by a series of replacement deletion vectors which target the hprt (hypoxanthine phosphoribosyltransferase) locus in mouse embryonic stem cells. We found that the targeting frequency of a 19.2-kb deletion was comparable to that of a 3-kb deletion or a conventional replacement event in which a 1.7-kb fragment was inserted into the locus. We also observed different integration patterns for these deletion vectors. A result of this finding is that a wide range of genomic deletions in embryonic stem cells is feasible.
我们分析了一系列针对小鼠胚胎干细胞中hprt(次黄嘌呤磷酸核糖转移酶)基因座的置换缺失载体所产生的基因靶向频率和重组产物。我们发现,19.2 kb缺失的靶向频率与3 kb缺失或向该基因座插入1.7 kb片段的传统置换事件的靶向频率相当。我们还观察到这些缺失载体的不同整合模式。这一发现的结果是,在胚胎干细胞中产生广泛的基因组缺失是可行的。