Colbere-Garapin F, Chousterman S, Horodniceanu F, Kourilsky P, Garapin A C
Proc Natl Acad Sci U S A. 1979 Aug;76(8):3755-9. doi: 10.1073/pnas.76.8.3755.
A herpes simplex virus DNA fragment that is produced by digestion with BamHI endonuclease and carries the thymidine kinase (TK; ATP:thymidine 5'-phosphotransferase, EC 2.7.1.21) gene has been cloned in Escherichia coli. A recombinat plasmid, pFG5, has been analyzed extensively and a detailed restriction map is presented. pFG5 DNA efficiently transforms TK- mouse L cells. The TK coding sequence in the cloned fragment has been localized and a smaller recombinant plasmid, pAG0, also carrying an active TK gene, has been constructed to serve as a more convenient vector for transfer, into TK- cells, of genes previously cloned in E. coli.
用BamHI核酸内切酶消化产生的、携带胸苷激酶(TK;ATP:胸苷5'-磷酸转移酶,EC 2.7.1.21)基因的单纯疱疹病毒DNA片段已克隆到大肠杆菌中。对重组质粒pFG5进行了广泛分析,并给出了详细的限制性图谱。pFG5 DNA能有效地转化TK-小鼠L细胞。已确定克隆片段中的TK编码序列,并构建了一个也携带活性TK基因的较小重组质粒pAG0,作为一种更方便的载体,用于将先前在大肠杆菌中克隆的基因转移到TK-细胞中。