Institut Pasteur, Unité de Génétique Moléculaire des Virus à ARN, Département de Virologie, F-75015 Paris, France; CNRS UMR3569, F-75015 Paris, France; Université Paris Diderot, Sorbonne Paris Cité EA302, F-75015 Paris, France.
INSERM U1028; CNRS UMR5292, Lyon Neuroscience Research Center, Genetic of Neuro-development Anomalies Team, F-69000 Lyon, France; Université Claude Bernard Lyon 1, CNRS UMR5558, Laboratoire de Biométrie et Biologie Evolutive, F-69622 Villeurbanne, France; EPI ERABLE, INRIA Grenoble Rhône-Alpes, F-38330 Montbonnot Saint-Martin, France.
Trends Microbiol. 2019 Mar;27(3):268-281. doi: 10.1016/j.tim.2018.11.004. Epub 2018 Dec 19.
Alteration of host cell splicing is a common feature of many viral infections which is underappreciated because of the complexity and technical difficulty of studying alternative splicing (AS) regulation. Recent advances in RNA sequencing technologies revealed that up to several hundreds of host genes can show altered mRNA splicing upon viral infection. The observed changes in AS events can be either a direct consequence of viral manipulation of the host splicing machinery or result indirectly from the virus-induced innate immune response or cellular damage. Analysis at a higher resolution with single-cell RNAseq, and at a higher scale with the integration of multiple omics data sets in a systems biology perspective, will be needed to further comprehend this complex facet of virus-host interactions.
宿主细胞剪接的改变是许多病毒感染的共同特征,但由于研究选择性剪接(AS)调控的复杂性和技术难度,这一特征尚未得到充分认识。最近 RNA 测序技术的进步表明,多达数百个宿主基因在病毒感染后会出现 mRNA 剪接的改变。观察到的 AS 事件的变化既可以是病毒直接操纵宿主剪接机制的结果,也可以间接地由病毒诱导的先天免疫反应或细胞损伤引起。需要通过单细胞 RNAseq 进行更高分辨率的分析,以及通过系统生物学视角整合多个组学数据集进行更高规模的分析,才能进一步理解病毒-宿主相互作用的这一复杂方面。