Hirai K, Lehman J M, Defendi V
J Virol. 1971 Dec;8(6):828-35. doi: 10.1128/JVI.8.6.828-835.1971.
The infection of secondary cultures of Chinese hamster cells with simian virus 40 (SV40) induces the appearance of cells with polyploid deoxyribonucleic acid (DNA) content or chromosomal component within one cell generation. The mechanism of this phenomenon was studied by the use of 5-bromodeoxyuridine (BUdR) incorporation as a DNA density marker. When cultures were treated with (14)C-BUdR and colcemide and harvested at 48 hr postinfection, only hybrid and light DNA molecules were found in control cultures, whereas in infected cultures there were also heavy molecules. The proportion of heavy DNA synthesized during the experimental period varied from 13 to 25%. It was determined by DNA-DNA hybridization that the heavy DNA consisted of cellular DNA. In radioautographic experiments, it was shown that, under the conditions used, a fraction of the infected cell population twice replicated its complete DNA content. Analysis of the kinetics indicated that the heavy DNA resulted from the reinitiation of DNA synthesis after the initial replication of the entire cell DNA. It was concluded that, after infection with SV40, a fraction of the Chinese hamster cell population undergoes two cycles of DNA synthesis without intervening mitosis.
用猴病毒40(SV40)感染中国仓鼠细胞的传代培养物,在一个细胞世代内可诱导出现具有多倍体脱氧核糖核酸(DNA)含量或染色体组成的细胞。利用5-溴脱氧尿苷(BUdR)掺入作为DNA密度标记来研究这种现象的机制。当培养物用(14)C-BUdR和秋水仙酰胺处理,并在感染后48小时收获时,在对照培养物中仅发现杂种和轻DNA分子,而在感染的培养物中也有重分子。实验期间合成的重DNA比例在13%至25%之间变化。通过DNA-DNA杂交确定重DNA由细胞DNA组成。在放射自显影实验中表明,在所使用的条件下,一部分受感染的细胞群体两次复制其完整的DNA含量。动力学分析表明,重DNA是在整个细胞DNA初始复制后DNA合成重新起始的结果。得出的结论是,感染SV-40后,一部分中国仓鼠细胞群体经历两个DNA合成周期而不发生中间的有丝分裂。