Richardson W D, Westphal H
J Virol. 1984 Aug;51(2):404-10. doi: 10.1128/JVI.51.2.404-410.1984.
Several adenovirus early genes act together to promote growth of the helper-dependent adeno-associated virus (AAV). Data from several laboratories have implicated adenovirus early regions 1a, 1b, 2a, and 4 in the helper effect, as well as the small RNA polymerase III transcript, virus-associated RNA I. Although a subset of these must participate directly in the AAV life cycle, some may play an indirect role by influencing expression of the others. This paper is concerned particularly with the roles of early regions 1a and 1b in the helper effect. We introduced DNA fragments representing the various early regions into AAV-infected or uninfected Vero cells, by the manual microinjection procedure. After labeling the cells with [35S]methionine, we visualized immunoprecipitates of AAV or adenovirus proteins on sodium dodecyl sulfate-polyacrylamide gels. When over 200 copies of each DNA fragment per cell were injected, early regions 2a and 4 were themselves sufficient to provide the helper effect. At 100 copies per cell, however, a third gene became essential, and this could be either early region 1a or 1b. The role of early region 1a is easily explained by its known ability to stimulate transcription of the other early genes. The function of early region 1b is less clear, but it does not simply mimic the action of early region 1a. Instead, there appear to be at least two distinct regulatory pathways which can lead to expression of AAV. To investigate the sequence of regulatory interactions, we microinjected purified adenovirus mRNAs, or combinations of mRNA and DNA, into AAV-infected cells. Our results suggest that adenovirus early products enhance viral gene expression by several mechanisms which can operate independently, but whose effects may be cumulative.
几种腺病毒早期基因共同作用以促进依赖辅助病毒的腺相关病毒(AAV)的生长。多个实验室的数据表明,腺病毒早期区域1a、1b、2a和4以及小RNA聚合酶III转录本病毒相关RNA I参与了辅助作用。虽然其中一部分必定直接参与AAV的生命周期,但有些可能通过影响其他基因的表达发挥间接作用。本文特别关注早期区域1a和1b在辅助作用中的角色。我们通过手动显微注射程序,将代表各个早期区域的DNA片段导入感染或未感染AAV的Vero细胞。在用[35S]甲硫氨酸标记细胞后,我们在十二烷基硫酸钠-聚丙烯酰胺凝胶上观察AAV或腺病毒蛋白的免疫沉淀。当每个细胞注射超过200个拷贝的每个DNA片段时,早期区域2a和4自身就足以提供辅助作用。然而,当每个细胞100个拷贝时,第三个基因变得至关重要,这个基因可以是早期区域1a或1b。早期区域1a的作用可以很容易地通过其刺激其他早期基因转录的已知能力来解释。早期区域1b的功能尚不清楚,但它并非简单地模仿早期区域1a的作用。相反,似乎至少有两条不同的调控途径可导致AAV的表达。为了研究调控相互作用的顺序,我们将纯化的腺病毒mRNA或mRNA与DNA的组合显微注射到感染AAV的细胞中。我们的结果表明,腺病毒早期产物通过几种可以独立起作用但其效应可能累积的机制增强病毒基因表达。