Department of Microbiology, New York University School of Medicine, New York, NY, United States.
Adv Virus Res. 2022;112:87-114. doi: 10.1016/bs.aivir.2022.01.002. Epub 2022 Mar 7.
Methylation at the N-position of either adenosine (mA) or 2'-O-methyladenosine (mAm) represents two of the most abundant internal modifications of coding and non-coding RNAs, influencing their maturation, stability and function. Additionally, although less abundant and less well-studied, monomethylation at the N-position (mA) can have profound effects on RNA folding. It has been known for several decades that RNAs produced by both DNA and RNA viruses can be mA/mAm modified and the list continues to broaden through advances in detection technologies and identification of the relevant methyltransferases. Recent studies have uncovered varied mechanisms used by viruses to manipulate the mA pathway in particular, either to enhance virus replication or to antagonize host antiviral defenses. As such, RNA modifications represent an important frontier of exploration in the broader realm of virus-host interactions, and this new knowledge already suggests exciting opportunities for therapeutic intervention. In this review we summarize the principal mechanisms by which mA/mAm can promote or hinder viral replication, describe how the pathway is actively manipulated by biomedically important viruses, and highlight some remaining gaps in understanding how adenosine methylation of RNA controls viral replication and pathogenesis.
N 位甲基化的腺苷(mA)或 2'-O-甲基腺苷(mAm)代表了编码和非编码 RNA 中最丰富的两种内部修饰方式,影响它们的成熟、稳定性和功能。此外,尽管丰度较低且研究较少,但 N 位的单甲基化(mA)可以对 RNA 折叠产生深远的影响。几十年来,人们已经知道 DNA 和 RNA 病毒产生的 RNA 可以被 mA/mAm 修饰,并且随着检测技术的进步和相关甲基转移酶的鉴定,这一列表不断扩大。最近的研究揭示了病毒用于操纵 mA 途径的各种机制,这些机制要么增强病毒复制,要么拮抗宿主抗病毒防御。因此,RNA 修饰代表了病毒-宿主相互作用这一更广泛领域探索的重要前沿,这一新知识已经为治疗干预提供了令人兴奋的机会。在这篇综述中,我们总结了 mA/mAm 促进或阻碍病毒复制的主要机制,描述了该途径如何被重要的生物医学病毒主动操纵,并强调了在理解 RNA 腺苷甲基化如何控制病毒复制和发病机制方面仍然存在一些空白。