Qasba P K
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1045-9. doi: 10.1073/pnas.71.4.1045.
Nuclei isolated from African green monkey kidney cells infected with simian virus 40 at different times after infection maintain in vitro the same temporal sequence of host and viral DNA synthesis as that seen in intact cells. The viral DNA synthesized by the nuclei of cells previously infected for 32-35 hr was characterized by centrifugation through neutral and alkaline sucrose gradients, and by isopycnic banding in a propidium iodide-cesium chloride gradient. DNA synthesis in this system is maintained for only 4-5 min. Neutral sucrose gradient analysis showed that most of the radioactivity is associated with the replicative intermediate of simian virus 40 DNA and the rest sediments at 5-7 S. Alkaline gradient analysis showed that 50-60% of the radioactivity sediments as 3-7S fragments, and the rest between 7 and 16 S. Pulsechase experiments showed that in this system 3-7S fragments do not mature into long chains. A model is presented to explain the failure of these fragments to join into long chains in this in vitro nuclear system.
从感染猿猴病毒40不同时间后的非洲绿猴肾细胞中分离出的细胞核,在体外维持着与完整细胞中所见相同的宿主和病毒DNA合成的时间顺序。通过中性和碱性蔗糖梯度离心以及在碘化丙啶-氯化铯梯度中的等密度沉降,对先前感染32-35小时的细胞的细胞核合成的病毒DNA进行了表征。该系统中的DNA合成仅维持4-5分钟。中性蔗糖梯度分析表明,大部分放射性与猿猴病毒40 DNA的复制中间体相关,其余部分在5-7 S沉降。碱性梯度分析表明,50-60%的放射性以3-7S片段沉降,其余部分在7至16 S之间沉降。脉冲追踪实验表明,在该系统中,3-7S片段不会成熟成长链。提出了一个模型来解释这些片段在该体外核系统中无法连接成长链的原因。