Francke B, Hunter T
J Virol. 1974 Jan;13(1):241-3. doi: 10.1128/JVI.13.1.241-243.1974.
The polyoma ts-a function was investigated by using an in vitro DNA-synthesizing system. A comparison of systems derived from ts25 (a ts-a group mutant)-and ts1260 (a late group mutant)-infected cells showed that the activation energies for DNA chain elongation and the mechanisms of discontinous growth were identical for both mutants.
利用体外DNA合成系统对多瘤病毒ts-a功能进行了研究。对源自ts25(ts-a组突变体)和ts1260(晚期组突变体)感染细胞的系统进行比较,结果表明,这两种突变体的DNA链延伸活化能和不连续生长机制是相同的。