Oda K, Fukui Y, Saito I, Masuda M, Shiroki K, Shimojo H
J Virol. 1983 Jan;45(1):420-7. doi: 10.1128/JVI.45.1.420-427.1983.
Simian virus 40 recombinant DNAs carrying the adenovirus type 12 E1B gene were constructed, propagated, and packaged in monkey cells. Monkey cells infected with the resulting virus stocks hyperproduced the E1B gene products in more than 80% of the cells as revealed by immunofluorescence. The products were distributed in both the nuclei and the cytoplasm, and a condensed form of fleck structure was observed in the cytoplasm. Polyacrylamide gel electrophoresis of the cell extracts and their immunoprecipitates detected the E1B-coded 19,000-molecular-weight protein but not the 50,000-molecular-weight protein. The 19,000-molecular-weight protein and the simian virus 40 VP1 protein were synthesized in nearly equal amounts.
构建了携带腺病毒12型E1B基因的猿猴病毒40重组DNA,并在猴细胞中进行繁殖和包装。用所得病毒株感染的猴细胞,通过免疫荧光显示,超过80%的细胞中E1B基因产物过度产生。这些产物分布在细胞核和细胞质中,并且在细胞质中观察到一种浓缩形式的斑点结构。对细胞提取物及其免疫沉淀物进行聚丙烯酰胺凝胶电泳,检测到E1B编码的19,000分子量的蛋白质,但未检测到50,000分子量的蛋白质。19,000分子量的蛋白质和猿猴病毒40 VP1蛋白的合成量几乎相等。