Hudziak R M, Laski F A, RajBhandary U L, Sharp P A, Capecchi M R
Cell. 1982 Nov;31(1):137-46. doi: 10.1016/0092-8674(82)90413-5.
We describe the generation of mammalian cell lines carrying amber suppressor genes. Nonsense mutants in the herpes simplex virus thymidine kinase (HSV tk) gene, the Escherichia coli xanthine-guanine phosphoribosyl transferase (Eco-gpt) gene and the aminoglycoside 3' phosphotransferase gene of the Tn5 transposon (NPT-II) were isolated and characterized. Each gene was engineered with the appropriate control signals to allow expression in both E. coli and mammalian cells. Expression in E. coli made possible the use of well developed bacterial and phage genetic manipulations to isolate and characterize the nonsense mutants. Once characterized, the nonsense mutants were transferred into mammalian cells by microinjection and used, in turn, to select for amber suppressor genes. Xenopus laevis amber suppressor genes, prepared by site-specific mutagenesis of a normal X. laevis tRNA gene, were microinjected into the above cell lines and selected for the expression of one or more of the amber mutant gene products. The resulting cell lines, containing functional amber suppressor genes, are stable and exhibit normal growth rates.
我们描述了携带琥珀抑制基因的哺乳动物细胞系的产生。分离并鉴定了单纯疱疹病毒胸苷激酶(HSV tk)基因、大肠杆菌黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(Eco - gpt)基因以及Tn5转座子的氨基糖苷3'磷酸转移酶基因(NPT - II)中的无义突变体。每个基因都配备了适当的控制信号,以便在大肠杆菌和哺乳动物细胞中表达。在大肠杆菌中的表达使得利用成熟的细菌和噬菌体遗传操作来分离和鉴定无义突变体成为可能。一旦鉴定完成,无义突变体通过显微注射转移到哺乳动物细胞中,进而用于筛选琥珀抑制基因。通过对正常非洲爪蟾tRNA基因进行位点特异性诱变制备的非洲爪蟾琥珀抑制基因,被显微注射到上述细胞系中,并筛选出一种或多种琥珀突变基因产物的表达。由此产生的含有功能性琥珀抑制基因的细胞系是稳定的,并且具有正常的生长速率。