Letellier C
Institut National de Recherches Vétérinaires, Uccle, Belgium.
Arch Virol. 1993;131(3-4):431-9. doi: 10.1007/BF01378643.
Insertion of foreign DNA containing the E. coli gpt marker by homologous recombination in the pigeonpox virus (PPV) thymidine kinase (TK) gene and selection for the presence of this DNA in the viral genome produced unstable recombinants after 3 plaque purifications. We highlight the persistence of duplicated TK DNA sequences arising from single crossing over, due to the growth advantage of TK+ virus. Restoration of the TK function by coinsertion of the vaccinia virus TK gene led to stable TK+ recombinants arising from double crossing over.
通过同源重组将含有大肠杆菌gpt标记的外源DNA插入鸽痘病毒(PPV)胸苷激酶(TK)基因,并在病毒基因组中选择该DNA的存在,经过3次噬斑纯化后产生了不稳定的重组体。由于TK +病毒的生长优势,我们强调了由单交换产生的重复TK DNA序列的持续性。通过共插入痘苗病毒TK基因恢复TK功能,导致由双交换产生稳定的TK +重组体。