Anderson R A, Krakauer T, Camerini-Otero R D
Proc Natl Acad Sci U S A. 1982 May;79(9):2748-52. doi: 10.1073/pnas.79.9.2748.
Ltk- aprt- mouse L cells were transformed to the tk+ phenotype with 10 ng of the herpes simplex virus-1 thymidine kinase (tk) gene and 20 micrograms of pBR322 or simian virus 40 (SV40) DNA. DNAs from five cloned cell lines show restriction endonuclease fragments that hybridize to both tk and pBR322 or SV40 DNA. In all of the cell lines some of these fragments also contain cellular DNA sequences. The use of carrier DNAs with defined sequences has enabled us to demonstrate that the joining of carrier and selectable gene sequences occurs in mouse cells. In one case we have been able to use the ampicillin resistance marker of pBR322 to "rescue" a recombinant plasmid. An analysis of the junction between pBR322 and tk in this plasmid suggests that a small area of homology (16 of 19 base pairs) might be involved in the recombination process.
用10纳克单纯疱疹病毒1型胸苷激酶(tk)基因以及20微克pBR322或猿猴病毒40(SV40)DNA将Ltk - aprt - 小鼠L细胞转化为tk + 表型。来自五个克隆细胞系的DNA显示出与tk以及pBR322或SV40 DNA杂交的限制性内切酶片段。在所有细胞系中,这些片段中的一些还包含细胞DNA序列。使用具有确定序列的载体DNA使我们能够证明载体和可选择基因序列的连接发生在小鼠细胞中。在一个案例中,我们能够利用pBR322的氨苄青霉素抗性标记来“拯救”一个重组质粒。对该质粒中pBR322和tk之间连接点的分析表明,一小段同源区域(19个碱基对中的16个)可能参与了重组过程。