Mukherjee A B, Orloff S, Butler J D, Triche T, Lalley P, Schulman J D
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1361-5. doi: 10.1073/pnas.75.3.1361.
Transfer of genes from one type of cultured mammalian cell to another by using isolated metaphase chromosomes has been reported with a frequency of one per 10(6)-10(8) cells. Very recently a rate of 16/10(6) has been reported with Chinese hamster ovary cells [Spandidos, D. A. & Siminovitch, L. (1977) Proc. Natl. Acad. Sci. USA 74, 3480-3484]. To increase the frequency of gene transfer, we isolated metaphase chromosomes from hypoxanthine guanine phosphoribosyltransferase (HGPRT) positive cells, entrapped them in liposomes, and fused the lipochromosomes with HGPRT-negative cells. Lipochromosomes were prepared with cholesterol and egg lecithin, using isolated metaphase chromosomes from a mouse-human somatic hybrid cell line (A9/HRBC2); the entire X chromosome, including the HGPRT, glucose-6-phosphate dehydrogenase, and phosphoglycerate kinase genes, is the only recognizable human genetic material retained by the hybrids. Enclosure of the chromosomes in the lipid envelope was confirmed by electron and fluorescence microscopy and differential centrifugation. These lipochromosomes were fused with HGPRT(-) mouse cells (A9) in the presence or absence of polyethylene glycol and transferents were selected in hypoxanthine/aminopterin/thymidine (HAT) medium. The frequency of transfer was at least once per 10(5) cells, a minimum 10-fold improvement over previous methods. The selected cells contained HGPRT activity similar to the amount found in the A9/HRBC2 cells. Starch gel electrophoresis verified that the observed HGPRT activity in the transferents is due to the human enzyme. Human glucose-6-phosphate dehydrogenase and phosphoglycerate kinase were also identified electrophoretically in the transferents. Karyotyping with C and Q banding did not reveal the presence of the whole human X chromosome or a visible extra fragment of a human chromosome associated with the mouse genome. The biochemical data strongly suggest, however, that transfer of a portion of the human X chromosome has occurred in these transferents. Thus, at least three X-linked genes have been transferred from one cell to another with high frequency, using metaphase chromosomes.
据报道,利用分离的中期染色体将基因从一种培养的哺乳动物细胞转移到另一种细胞,频率为每10⁶ - 10⁸个细胞中有一个成功转移。最近报道了中国仓鼠卵巢细胞的转移率为16/10⁶ [斯潘迪多斯,D. A.及西米诺维奇,L.(1977年)《美国国家科学院院刊》74, 3480 - 3484]。为了提高基因转移频率,我们从次黄嘌呤鸟嘌呤磷酸核糖基转移酶(HGPRT)阳性细胞中分离出中期染色体,将它们包裹在脂质体中,并使脂质染色体与HGPRT阴性细胞融合。脂质染色体是用胆固醇和卵磷脂制备的,使用的是从小鼠 - 人类体细胞杂种细胞系(A9/HRBC2)中分离出的中期染色体;整个X染色体,包括HGPRT、葡萄糖 - 6 - 磷酸脱氢酶和磷酸甘油酸激酶基因,是杂种细胞中唯一可识别的人类遗传物质。通过电子显微镜、荧光显微镜和差速离心法证实了染色体被包裹在脂质包膜中。在有或没有聚乙二醇的情况下,将这些脂质染色体与HGPRT( - )小鼠细胞(A9)融合,并在次黄嘌呤/氨基蝶呤/胸腺嘧啶核苷(HAT)培养基中筛选转移体。转移频率至少为每10⁵个细胞一次,比以前的方法至少提高了10倍。所选细胞所含的HGPRT活性与A9/HRBC2细胞中的活性量相似。淀粉凝胶电泳证实,转移体中观察到的HGPRT活性是由人类酶引起的。在转移体中还通过电泳鉴定出了人类葡萄糖 - 6 - 磷酸脱氢酶和磷酸甘油酸激酶。用C带和Q带进行核型分析未发现整个人类X染色体或与小鼠基因组相关的人类染色体可见额外片段的存在。然而,生化数据有力地表明,在这些转移体中发生了人类X染色体一部分的转移。因此,使用中期染色体已将至少三个X连锁基因从一个细胞高频转移到另一个细胞。