Sabourin D J, Davidson R L
Somatic Cell Genet. 1979 Mar;5(2):159-74. doi: 10.1007/BF01539158.
Thymidine kinase (TK)-deficient human cells were infected with ultraviolet light-inactivated Herpes simplex virus type 1, and "transformed" cells that expressed Herpes TK activity were isolated. Purified metaphase chromosomes were isolated from the transformed human line and incubated with TK-deficient mouse cells. TK+ cells were selected, and it was shown that these cells were gene transferents which expressed Herpes TK activity, identical to that found in the transformed human cells. The gene transferents contained no intact human chromosomes. When removed from selective pressure, the gene transferents rapidly lost the TK+ phenotype. However, upon continued growth in nonselective medium, a subpopulation in which the TK+ phenotype had become more stabilized appeared. These results suggest that the Herpes gene for thymidine kinase has integrated into the genome of the HSV-transformed human cells and that it can be transferred to other cells by means of purified metaphase chromosomes.
用紫外线灭活的单纯疱疹病毒1型感染胸苷激酶(TK)缺陷的人类细胞,然后分离出表达疱疹TK活性的“转化”细胞。从转化的人类细胞系中分离出纯化的中期染色体,并与TK缺陷的小鼠细胞一起孵育。选择出TK+细胞,结果表明这些细胞是表达疱疹TK活性的基因转移体,其活性与在转化的人类细胞中发现的相同。这些基因转移体不包含完整的人类染色体。当去除选择压力时,基因转移体迅速失去TK+表型。然而,在非选择性培养基中持续生长时,出现了一个亚群,其中TK+表型变得更加稳定。这些结果表明,疱疹胸苷激酶基因已整合到HSV转化的人类细胞基因组中,并且它可以通过纯化的中期染色体转移到其他细胞中。