Ono Chikako, Sato Masanao, Taka Hitomi, Asano Shin-ichiro, Matsuura Yoshiharu, Bando Hisanori
Laboratory of Applied Molecular Entomology, Division of Applied Bioscience, Graduate School of Agriculture, Hokkaido University, Sapporo, Japan.
National Institute for Basic Biology, Okazaki Institute for Integrative Bioscience, National Institutes of Natural Sciences, Higashiyama, Myodaiji, Okazaki, Japan.
PLoS One. 2015 Mar 27;10(3):e0119580. doi: 10.1371/journal.pone.0119580. eCollection 2015.
To infect their hosts, DNA viruses must successfully initiate the expression of viral genes that control subsequent viral gene expression and manipulate the host environment. Viral genes that are immediately expressed upon infection play critical roles in the early infection process. In this study, we investigated the expression and regulation of five canonical regulatory immediate-early (IE) genes of Autographa californica multicapsid nucleopolyhedrovirus: ie0, ie1, ie2, me53, and pe38. A systematic transient gene-expression analysis revealed that these IE genes are generally transactivators, suggesting the existence of a highly interactive regulatory network. A genetic analysis using gene knockout viruses demonstrated that the expression of these IE genes was tolerant to the single deletions of activator IE genes in the early stage of infection. A network graph analysis on the regulatory relationships observed in the transient expression analysis suggested that the robustness of IE gene expression is due to the organization of the IE gene regulatory network and how each IE gene is activated. However, some regulatory relationships detected by the genetic analysis were contradictory to those observed in the transient expression analysis, especially for IE0-mediated regulation. Statistical modeling, combined with genetic analysis using knockout alleles for ie0 and ie1, showed that the repressor function of ie0 was due to the interaction between ie0 and ie1, not ie0 itself. Taken together, these systematic approaches provided insight into the topology and nature of the IE gene regulatory network.
为了感染宿主,DNA病毒必须成功启动控制后续病毒基因表达并操纵宿主环境的病毒基因的表达。感染后立即表达的病毒基因在早期感染过程中发挥关键作用。在本研究中,我们调查了苜蓿银纹夜蛾多粒包埋核型多角体病毒的五个典型调控立即早期(IE)基因的表达和调控:ie0、ie1、ie2、me53和pe38。系统的瞬时基因表达分析表明,这些IE基因通常是反式激活因子,这表明存在一个高度交互的调控网络。使用基因敲除病毒的遗传分析表明,在感染早期,这些IE基因的表达对激活因子IE基因的单缺失具有耐受性。对瞬时表达分析中观察到的调控关系进行的网络图分析表明,IE基因表达的稳健性归因于IE基因调控网络的组织方式以及每个IE基因的激活方式。然而,遗传分析检测到的一些调控关系与瞬时表达分析中观察到的关系相矛盾,尤其是对于IE0介导的调控。统计建模与使用ie0和ie1的敲除等位基因的遗传分析相结合,表明ie0的阻遏功能是由于ie0和ie1之间的相互作用,而不是ie0本身。综上所述,这些系统方法为IE基因调控网络的拓扑结构和性质提供了深入了解。