Brown M, McCormack M, Zinn K G, Farrell M P, Bikel I, Livingston D M
J Virol. 1986 Oct;60(1):290-3. doi: 10.1128/JVI.60.1.290-293.1986.
A recombinant murine retrovirus containing the intact cDNA sequence for the simian virus 40 (SV40) large T antigen (T) was constructed by using the pZIPNeo SV(X)1 vector. Psi 2 packaging cells were then transfected, and G418-resistant clones were used to generate helper-free viral stocks. NIH 3T3 mouse fibroblasts infected by the recombinant T cDNA retrovirus were selected fro G418 resistance. Such cultures synthesized authentic SV40 T and were transformed to anchorage-independent growth at high efficiency. Therefore, this vector has allowed the study of the transformation properties of T under conditions of neutral drug selection and in the absence of SV40 small t antigen.
利用pZIPNeo SV(X)1载体构建了一种重组鼠逆转录病毒,其包含猿猴病毒40(SV40)大T抗原(T)的完整cDNA序列。然后转染Psi 2包装细胞,并用对G418有抗性的克隆来制备无辅助病毒的病毒储备液。选择受重组T cDNA逆转录病毒感染且对G418有抗性的NIH 3T3小鼠成纤维细胞。此类培养物合成了真实的SV40 T,并高效转化为不依赖贴壁的生长状态。因此,该载体使得在中性药物选择条件下且不存在SV40小t抗原的情况下研究T的转化特性成为可能。