Pavan W J, Hieter P, Reeves R H
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2196.
Mol Cell Biol. 1990 Aug;10(8):4163-9. doi: 10.1128/mcb.10.8.4163-4169.1990.
A neomycin resistance cassette was integrated into the human-derived insert of a 360-kilobase yeast artificial chromosome (YAC) by targeting homologous recombination to Alu repeat sequences. The modified YAC was transferred into an embryonal carcinoma cell line by using polyethylene glycol-mediated spheroplast fusion. A single copy of the human sequence was introduced intact and stably maintained in the absence of selection for over 40 generations. A substantial portion of the yeast genome was retained in hybrids in addition to the YAC. Hybrid cells containing the YAC retained the ability to differentiate when treated with retinoic acid. This approach provides a powerful tool for in vitro analysis because it can be used to modify any human DNA cloned as a YAC and to transfer large fragments of DNA intact into cultured mammalian cells, thereby facilitating functional studies of genes in the context of extensive flanking DNA sequences.
通过将同源重组靶向至Alu重复序列,将新霉素抗性盒整合到一个360千碱基酵母人工染色体(YAC)的人源插入片段中。使用聚乙二醇介导的原生质球融合法将修饰后的YAC转入一个胚胎癌细胞系。完整地引入了单拷贝的人源序列,并且在无选择压力的情况下稳定维持了40多代。除了YAC之外,相当一部分酵母基因组也保留在杂种细胞中。含有YAC的杂种细胞在用视黄酸处理时保留了分化能力。这种方法为体外分析提供了一个强大的工具,因为它可用于修饰作为YAC克隆的任何人类DNA,并将大片段DNA完整地转入培养的哺乳动物细胞,从而便于在广泛的侧翼DNA序列背景下对基因进行功能研究。