Laboratory of Virology and Immunology, GIGA-Research, University of Liège (ULg), B-4000 Liège, Belgium.
Biochem Pharmacol. 2010 Dec 15;80(12):1973-80. doi: 10.1016/j.bcp.2010.07.011. Epub 2010 Jul 27.
During a viral infection, in addition to cellular mRNAs, amounts of viral mRNAs have to be efficiently transported to the cytoplasm for translation. It is now established that herpesviruses encode a conserved gene family whose proteins act as viral mRNA export factors that mediate nucleocytoplasmic transport of viral transcripts and eventually modulate through this mechanism the antiviral response. This conserved family of proteins contains the IE4 protein of the Varicella-Zoster virus (VZV). Here, we compared the functional characteristics of IE4 with those of its herpesviral homologues and proposed a model by which IE4 would be able to recruit the essential TAP/NXF1 receptor to viral transcripts. Moreover, on the basis of their crucial roles in the infectious cycle, these conserved viral factors should be considered as alternative targets in therapeutic approaches. Here, we discussed the possibility of developing antiherpetic agents targeting IE4 or its herpesviral homologues.
在病毒感染过程中,除了细胞 mRNA,还必须将大量的病毒 mRNA 有效地转运到细胞质中进行翻译。目前已经确定,疱疹病毒编码了一个保守的基因家族,其蛋白质作为病毒 mRNA 输出因子,介导病毒转录物的核质转运,并最终通过这种机制调节抗病毒反应。这个保守的蛋白家族包含了水痘带状疱疹病毒(VZV)的 IE4 蛋白。在这里,我们比较了 IE4 与其疱疹病毒同源物的功能特征,并提出了一个模型,即 IE4 能够招募必需的 TAP/NXF1 受体到病毒转录物上。此外,基于它们在感染周期中的关键作用,这些保守的病毒因子应该被视为治疗方法中的替代靶标。在这里,我们讨论了针对 IE4 或其疱疹病毒同源物开发抗疱疹药物的可能性。