Stanton B R, Reid S W, Parada L F
Molecular Embryology Group, NCI-Frederick Cancer Research and Development Center, Maryland 21702-1201.
Mol Cell Biol. 1990 Dec;10(12):6755-8. doi: 10.1128/mcb.10.12.6755-6758.1990.
We have disrupted one allele of the N-myc locus in mouse embryonic stem (ES) cells by using homologous recombination techniques and have obtained germ line transmission of null N-myc ES cell lines with transmission of the null N-myc allele to the offspring. The creation of mice with a deficient N-myc allele will allow the generation of offspring bearing null N-myc alleles in both chromosomes and permit study of the role that this proto-oncogene plays in embryonic development.
我们利用同源重组技术在小鼠胚胎干细胞(ES细胞)中破坏了N-myc基因座的一个等位基因,并获得了无效N-myc ES细胞系的种系传递,无效N-myc等位基因传递给了后代。创建具有缺陷N-myc等位基因的小鼠将能够产生两条染色体上均带有无效N-myc等位基因的后代,并允许研究这个原癌基因在胚胎发育中所起的作用。