Institute for Virology and Immunobiology, Julius-Maximilians-University Würzburg, 97078 Würzburg, Germany.
Helmholtz Center for Infection Research (HZI), Helmholtz Institute for RNA-Based Infection Research (HIRI), 97080 Würzburg, Germany.
Viruses. 2021 Sep 14;13(9):1836. doi: 10.3390/v13091836.
During lytic infection, herpes simplex virus (HSV) 1 induces a rapid shutoff of host RNA synthesis while redirecting transcriptional machinery to viral genes. In addition to being a major human pathogen, there is burgeoning clinical interest in HSV as a vector in gene delivery and oncolytic therapies, necessitating research into transcriptional control. This review summarizes the array of impacts that HSV has on RNA Polymerase (Pol) II, which transcribes all mRNA in infected cells. We discuss alterations in Pol II holoenzymes, post-translational modifications, and how viral proteins regulate specific activities such as promoter-proximal pausing, splicing, histone repositioning, and termination with respect to host genes. Recent technological innovations that have reshaped our understanding of previous observations are summarized in detail, along with specific research directions and technical considerations for future studies.
在裂解感染过程中,单纯疱疹病毒 1(HSV)会迅速关闭宿主的 RNA 合成,同时将转录机制重新定向到病毒基因。除了是主要的人类病原体之外,HSV 作为基因传递和溶瘤治疗的载体,在临床上也越来越受到关注,这就需要对转录控制进行研究。本综述总结了 HSV 对 RNA 聚合酶(Pol)II 的一系列影响,Pol II 转录感染细胞中的所有 mRNA。我们讨论了 Pol II 全酶的改变、翻译后修饰,以及病毒蛋白如何调节特定活性,如启动子近端暂停、剪接、组蛋白重定位和终止与宿主基因的关系。详细总结了最近重塑我们对先前观察结果的理解的技术创新,并提出了未来研究的具体研究方向和技术考虑。