Kit G, Daniell E
J Virol. 1978 Jul;27(1):74-80. doi: 10.1128/JVI.27.1.74-80.1978.
The acid extraction of the adenovirus type 5 core proteins V, VII, and pVII (the precursor to VII) from infected cells and the subsequent electrophoresis on a 15% acrylamide-2.5 M urea-0.9 N acetic acid (pH 2.7) gel, revealed that peptide VII has a similar electrophoretic mobility to that of histone H1. The core proteins, which are coded by late adenovirus mRNA, continued to be synthesized late in infection when viral DNA synthesis was inhibited either by cytosine arabinoside in wild-type infections or by shifting adenovirus H5 ts 125-infected cells to the nonpermissive temperature (40 degree C). Only the initiation, not the continuation, of viral DNA replication was essential for core protein synthesis. The synthesis of viral core proteins continued for over 8 h after the cassation of DNA synthesis. This was in contrast to the rapid shutdown of cellular histone synthesis in the absence of cellular DNA synthesis.
从感染细胞中酸提取5型腺病毒核心蛋白V、VII和pVII(VII的前体),随后在15%丙烯酰胺-2.5M尿素-0.9N乙酸(pH 2.7)凝胶上进行电泳,结果显示肽VII与组蛋白H1具有相似的电泳迁移率。这些由腺病毒晚期mRNA编码的核心蛋白,在感染后期,当野生型感染中通过阿糖胞苷抑制病毒DNA合成,或在腺病毒H5 ts 125感染的细胞转移到非允许温度(40℃)时,仍持续合成。只有病毒DNA复制的起始,而非延续,对核心蛋白合成至关重要。在DNA合成停止后,病毒核心蛋白的合成持续了超过8小时。这与在无细胞DNA合成时细胞组蛋白合成的快速停止形成对比。