Tong Jie, Zhang Wuchao, Chen Yuran, Yuan Qiaoling, Qin Ning-Ning, Qu Guosheng
College of Life Sciences, Hebei University, Baoding, China.
Institute of Life Sciences and Green Development, Hebei University, Baoding, China.
Front Microbiol. 2022 Feb 3;13:845625. doi: 10.3389/fmicb.2022.845625. eCollection 2022.
Posttranscriptional modifications have been implicated in regulation of nearly all biological aspects of cellular RNAs, from stability, translation, splicing, nuclear export to localization. Chemical modifications also have been revealed for virus derived RNAs several decades before, along with the potential of their regulatory roles in virus infection. Due to the dynamic changes of RNA modifications during virus infection, illustrating the mechanisms of RNA epigenetic regulations remains a challenge. Nevertheless, many studies have indicated that these RNA epigenetic marks may directly regulate virus infection through antiviral innate immune responses. The present review summarizes the impacts of important epigenetic marks on viral RNAs, including N6-methyladenosine (mA), 5-methylcytidine (mC), 2'-O-methylation (2'-O-Methyl), and a few uncanonical nucleotides (A-to-I editing, pseudouridine), on antiviral innate immunity and relevant signaling pathways, while highlighting the significance of antiviral innate immune responses during virus infection.
转录后修饰几乎涉及细胞RNA的所有生物学方面的调控,包括稳定性、翻译、剪接、核输出和定位。几十年前就已发现病毒衍生RNA存在化学修饰,以及它们在病毒感染中潜在的调控作用。由于病毒感染过程中RNA修饰的动态变化,阐明RNA表观遗传调控机制仍然是一项挑战。然而,许多研究表明,这些RNA表观遗传标记可能通过抗病毒先天免疫反应直接调节病毒感染。本综述总结了重要表观遗传标记对病毒RNA的影响,包括N6-甲基腺苷(m6A)、5-甲基胞嘧啶(mC)、2'-O-甲基化(2'-O-Me)以及一些非典型核苷酸(A到I编辑、假尿苷)对抗病毒先天免疫和相关信号通路的影响,同时强调了病毒感染期间抗病毒先天免疫反应的重要性。