Graessmann M, Graessman A
Proc Natl Acad Sci U S A. 1976 Feb;73(2):366-70. doi: 10.1073/pnas.73.2.366.
Simian virus 40 (SV40) induces tumor (T)-antigen formation, chromatin replication, and mitosis in primary mouse kidney cells arrested in G0 phase of the mitotic cycle. The temporal and quantitative relation between these early virus-specific reactions led to the hypothesis that the early SV40 mRNA contains information necessary for T-antigen formation and induction of cellular DNA synthesis. To get direct experimental evidence for this hypothesis, the early strand of SV40 DNA was transcribed in vitro by Escherichia coli DNA-dependent RNA polymerase and the SV40-specific cRNA was transferred by microinjection into epitheloid cells of confluent primary mouse kidney cultures. T-antigen formation and stimulation of DNA synthesis were investigated in the recipient cells. The experimental results obtained agree with the hypothesis that T-antigen is a virus-coded protein and that the early virus-specific mRNA contains information necessary for stimulation of cellular DNA replication in the arrested cells.
猴病毒40(SV40)可在处于有丝分裂周期G0期的原代小鼠肾细胞中诱导肿瘤(T)抗原形成、染色质复制和有丝分裂。这些早期病毒特异性反应之间的时间和定量关系导致了这样一种假设,即早期SV40 mRNA包含T抗原形成和诱导细胞DNA合成所需的信息。为了获得这一假设的直接实验证据,用大肠杆菌DNA依赖性RNA聚合酶在体外转录SV40 DNA的早期链,并通过显微注射将SV40特异性cRNA转移到汇合的原代小鼠肾培养物的上皮样细胞中。在受体细胞中研究了T抗原形成和DNA合成的刺激情况。获得的实验结果与以下假设一致:T抗原是一种病毒编码蛋白,早期病毒特异性mRNA包含刺激停滞细胞中细胞DNA复制所需的信息。