Lindenmaier W, Hauser H, de Wilke I G, Schütz G
Nucleic Acids Res. 1982 Feb 25;10(4):1243-56. doi: 10.1093/nar/10.4.1243.
Successful shuttling of cloned DNA in eukaryotic cells should allow isolation of expressed genes. We tested the utility of cosmids for moving DNA into and out of eukaryotic cells. The unique cleavage of DNA at the cos site by the terminase function of lambda was exploited to maintain the linkage between the vector and inserted gene sequences, a prerequisite for successful rescue of the transforming DNA from high molecular weight DNA of the eukaryotic transformant. A cosmid recombinant containing the HSV thymidine kinase gene and a lambda recombinant containing the chicken thymidine kinase gene were used to test the feasability of this method. It was found that these recombinants can be rescued with high efficiency from DNA of HAT-resistant cells.
在真核细胞中成功穿梭克隆DNA应能实现对表达基因的分离。我们测试了黏粒在将DNA导入和导出真核细胞方面的效用。利用λ噬菌体的末端酶功能在黏粒位点对DNA进行独特切割,以维持载体与插入基因序列之间的连接,这是从真核转化体的高分子量DNA中成功拯救转化DNA的一个先决条件。使用含有单纯疱疹病毒胸苷激酶基因的黏粒重组体和含有鸡胸苷激酶基因的λ重组体来测试该方法的可行性。结果发现,这些重组体能够从对氨基蝶呤、氨甲蝶呤和胸腺嘧啶核苷有抗性的细胞的DNA中高效拯救出来。