Cheevers W P, Branton P E, Sheinin R
J Virol. 1970 Nov;6(5):573-82. doi: 10.1128/JVI.6.5.573-582.1970.
It was previously shown that the majority of deoxyribonucleic acid (DNA) made in growing mouse embryo cells productively infected at low multiplicity with polyoma virus is cellular in nature and that some of this cell DNA contains discontinuities in the newly synthesized strand. Evidence obtained indicates the following. (i) Induction of cell DNA synthesis precedes the onset of detectable viral DNA replication by approximately 3 hr. (ii) Double-stranded cell DNA molecules, discontinuous in the newly synthesized strands, arise by direct synthesis (rather than by degradation of a high-molecular-weight precursor) only in the cell DNA replicated after initiation of viral DNA synthesis. (iii) This DNA component is continuously formed throughout the "late" stage of infection and is continuously converted into apparently normal cell DNA of high molecular weight without prior degradation to acid-soluble components.
先前的研究表明,在以低感染复数被多瘤病毒有效感染的生长中的小鼠胚胎细胞中合成的大多数脱氧核糖核酸(DNA)本质上是细胞性的,并且这种细胞DNA中的一些在新合成的链中含有间断。所获得的证据表明如下情况。(i)细胞DNA合成的诱导比可检测到的病毒DNA复制的开始提前约3小时。(ii)仅在病毒DNA合成开始后复制的细胞DNA中,新合成链中具有间断的双链细胞DNA分子通过直接合成(而非高分子量前体的降解)产生。(iii)这种DNA成分在感染的“后期”持续形成,并持续转化为明显正常的高分子量细胞DNA,而无需事先降解为酸溶性成分。