Wilkie N M, Clements J B, Boll W, Mantei N, Lonsdale D, Weissmann C
Nucleic Acids Res. 1979 Oct 25;7(4):859-77. doi: 10.1093/nar/7.4.859.
The gene for the thymidine kinase (TK) of Herpes simplex virus type 1 (HSV-1) is located in the KpnI m and BamHI p fragments of the genome (Wigler et al., Cell 11, 223-232 (1977)). These fragments have been inserted into the EcoRI and BamHI sites, respectively, of plasmid pBR322, and propagated in E.coli. The TK gene contained in the recombinant plasmids was shown to be biologically active when introduced into TK- mouse L cells. Detailed restriction site maps of the BamHI p fragment have been constructed and the approximate location of the TK gene has been determined. Mouse cells transformed with cloned HSV-1 tk+ DNA produced HSV-1-specific thymidine kinase; superinfection with HSV-1 tk- virus increased the level of TK activity tenfold, suggesting that the BamHI p sequences present in transformed cells respond to virus-encoded regulatory gene product(s).
单纯疱疹病毒1型(HSV - 1)胸苷激酶(TK)基因位于基因组的KpnI m和BamHI p片段中(Wigler等人,《细胞》11卷,223 - 232页(1977年))。这些片段已分别插入质粒pBR322的EcoRI和BamHI位点,并在大肠杆菌中繁殖。当将重组质粒中包含的TK基因导入TK - 小鼠L细胞时,显示其具有生物活性。已构建了BamHI p片段的详细限制性酶切位点图谱,并确定了TK基因的大致位置。用克隆的HSV - 1 tk⁺ DNA转化的小鼠细胞产生了HSV - 1特异性胸苷激酶;用HSV - 1 tk⁻病毒进行超感染使TK活性水平提高了十倍,这表明转化细胞中存在的BamHI p序列对病毒编码的调节基因产物有反应。