Tegtmeyer P
J Virol. 1972 Oct;10(4):591-8. doi: 10.1128/JVI.10.4.591-598.1972.
Three temperature-sensitive (ts) mutants of simian virus 40 (SV40) in complementation group A (tsA7, tsA28, tsA30) have been isolated and characterized in permissive and restrictive host cells. At 41 C in the AH line of African green monkey kidney cells, the mutants are deficient in an early function required to produce infectious viral deoxyribonucleic acid (DNA). Temperature-shift experiments and analysis of SV40 viral DNA replication by gel electrophoresis have provided strong evidence that the ts gene product of the three mutants is directly required to initiate each new round of viral DNA replication but is not required to complete a cycle which has already begun. The synthesis of mutant DNA molecules themselves can be initiated by a nonmutant gene product in viral complementation studies at 41 C. The cell, however, cannot substitute a host function to provide the initiator required for the replication of free viral DNA. The viral initiator is also required to establish the stable transformation of 3T3 cells.
已在允许性和限制性宿主细胞中分离并鉴定了猿猴病毒40(SV40)互补群A中的三个温度敏感(ts)突变体(tsA7、tsA28、tsA30)。在非洲绿猴肾细胞的AH系中,于41℃时,这些突变体在产生传染性病毒脱氧核糖核酸(DNA)所需的早期功能方面存在缺陷。温度转换实验以及通过凝胶电泳对SV40病毒DNA复制的分析提供了有力证据,表明这三个突变体的ts基因产物是启动每一轮新的病毒DNA复制直接所需的,但完成已经开始的一个循环则不需要。在41℃的病毒互补研究中,突变DNA分子自身的合成可由非突变基因产物启动。然而,细胞无法替代宿主功能来提供游离病毒DNA复制所需的引发剂。病毒引发剂对于建立3T3细胞的稳定转化也是必需的。