Lassar A B, Paterson B M, Weintraub H
Cell. 1986 Dec 5;47(5):649-56. doi: 10.1016/0092-8674(86)90507-6.
Stable myoblast cell lines were isolated after a brief exposure of mouse fibroblasts (10T1/2 cells) to 5-azacytidine. We show that transfection of 10T1/2 cells with DNA from these azacytidine-induced myoblasts (or from mouse C2C12 myoblasts) results in myogenic conversion of approximately 1 in 15,000 transfected colonies. In contrast, transfection of 10T1/2 cells with DNA from nonmyogenic cells (parental 10T1/2 cell DNA) does not give rise to myoblast colonies. These results indicate that an azacytidine-induced structural modification (presumably demethylation) in the DNA of a single locus is sufficient to convert 10T1/2 cells into determined myoblasts.
在将小鼠成纤维细胞(10T1/2细胞)短暂暴露于5-氮杂胞苷后,分离出了稳定的成肌细胞系。我们发现,用这些经氮杂胞苷诱导的成肌细胞(或小鼠C2C12成肌细胞)的DNA转染10T1/2细胞,在大约15000个转染菌落中会有1个发生成肌转化。相比之下,用非成肌细胞的DNA(亲本10T1/2细胞DNA)转染10T1/2细胞则不会产生成肌细胞菌落。这些结果表明,单个基因座DNA中由氮杂胞苷诱导的结构修饰(可能是去甲基化)足以将10T1/2细胞转化为已确定的成肌细胞。