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Transfer of the gene for thymidine kinase to thymidine kinase-deficient human cells by purified herpes simplex viral DNA.

机译:纯化的单纯疱疹病毒DNA将胸苷激酶的基因转移到缺乏胸苷激酶的人细胞中。

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摘要

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.
机译:通过使用2型单纯疱疹病毒的纯化DNA实现了人类细胞从胸苷激酶(ATP:胸苷5'-磷酸转移酶,EC 2.7.1.75)阴性向胸苷激酶阳性表型的转化。 DNA的范围是每微克0.5到2.0个转化子,每10(5)个受体细胞中基因转移的效率高达1个转化子。已经建立了几种能够在对胸苷激酶阳性细胞具有选择性的培养基中连续生长的转化品系。所有这些系均表达病毒来源的胸苷激酶活性,但是它们在酶表达的稳定性方面彼此不同。从给定的转化品系衍生的亚克隆继承了亲本品系的稳定性。

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  • 作者

    Bacchetti, S; Graham, F L;

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  • 年度 1977
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  • 原文格式 PDF
  • 正文语种 en
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