Everett R D, Dunlop M
Nucleic Acids Res. 1984 Aug 10;12(15):5969-78. doi: 10.1093/nar/12.15.5969.
This paper describes experiments to test the ability of a number of viruses of the Herpes group, and also Adenovirus-2 and SV40, to activate transcription from the Herpes simplex virus-1 glycoprotein D and the rabbit beta-globin promoters. Plasmids containing these genes were transfected into HeLa cells which were then infected with various viruses. Transcriptional activation in trans of the plasmid-borne promoters was monitored by quantitative S1 nuclease analysis of total cytoplasmic RNA isolated after infection. The results showed that Herpes simplex viruses 1 and 2, Pseudorabies virus, Variella Zoster virus, Human Cytomegalovirus, Equine herpes virus-1 and Adenovirus-2 activate transcription from both promoters tested. In contrast, SV40 did not activate transcription in trans in this assay. The possible mechanisms of this activation are discussed.
本文描述了一系列实验,旨在测试多种疱疹病毒组病毒以及腺病毒2型和猿猴病毒40(SV40)激活单纯疱疹病毒1型糖蛋白D启动子和兔β-珠蛋白启动子转录的能力。将含有这些基因的质粒转染入HeLa细胞,随后用各种病毒感染这些细胞。通过对感染后分离的总细胞质RNA进行定量S1核酸酶分析,监测质粒携带启动子的反式转录激活情况。结果表明,单纯疱疹病毒1型和2型、伪狂犬病病毒、水痘带状疱疹病毒、人巨细胞病毒、马疱疹病毒1型和腺病毒2型均可激活所测试的两个启动子的转录。相比之下,在该实验中SV40未激活反式转录。文中讨论了这种激活可能的机制。