Bacchetti S, Graham F L
Proc Natl Acad Sci U S A. 1977 Apr;74(4):1590-4. doi: 10.1073/pnas.74.4.1590.
Transformation of human cells from a thymidine kinase (ATP:thymidine 5'-phosphotransferase, EC 2.7.1.75)-negative to a thymidine kinase-positive phenotype has been achieved by using purified DNA from herpes simplex virus type 2. The specific activity of the DNA was in the range 0.5 to 2.0 transformants per microng and the efficiency of gene transfer was up to 1 transformant per 10(5) recipient cells. Several transformed lines able to grow continuously in medium selective for thymidine kinase-positive cells have been established. All of these lines express a thymidine kinase activity of viral origin but they differ from each other in the stability of enzyme expression. Subclones derived from a given transformed line inherited the degree of stability of the parental line.
通过使用来自2型单纯疱疹病毒的纯化DNA,已实现将人细胞从胸苷激酶(ATP:胸苷5'-磷酸转移酶,EC 2.7.1.75)阴性转变为胸苷激酶阳性表型。DNA的比活性范围为每微克0.5至2.0个转化体,基因转移效率高达每10(5)个受体细胞1个转化体。已经建立了几个能够在对胸苷激酶阳性细胞有选择性的培养基中连续生长的转化细胞系。所有这些细胞系都表达病毒来源的胸苷激酶活性,但它们在酶表达的稳定性方面彼此不同。从给定转化细胞系衍生的亚克隆继承了亲代细胞系的稳定性程度。