Imam Hasan, Kim Geon-Woo, Siddiqui Aleem
Division of Infectious Diseases, Department of Medicine, University of California, San Diego, La Jolla, CA, United States.
Front Cell Infect Microbiol. 2020 Nov 24;10:584283. doi: 10.3389/fcimb.2020.584283. eCollection 2020.
N6-methyladenosine (mA) is the most prevalent and internal modification of eukaryotic mRNA. Multiple mA methylation sites have been identified in the viral RNA genome and transcripts of DNA viruses in recent years. mA modification is involved in all the phases of RNA metabolism, including RNA stability, splicing, nuclear exporting, RNA folding, translational modulation, and RNA degradation. Three protein groups, methyltransferases (mA-writers), demethylases (mA-erasers), and mA-binding proteins (mA-readers) regulate this dynamic reversible process. Here, we have reviewed the role of mA modification dictating viral replication, morphogenesis, life cycle, and its contribution to disease progression. A better understanding of the mA methylation process during viral pathogenesis is required to reveal novel approaches to combat the virus-associated diseases.
N6-甲基腺嘌呤(mA)是真核生物mRNA中最普遍的内部修饰。近年来,在病毒RNA基因组和DNA病毒转录本中已鉴定出多个mA甲基化位点。mA修饰参与RNA代谢的各个阶段,包括RNA稳定性、剪接、核输出、RNA折叠、翻译调控和RNA降解。三类蛋白质,即甲基转移酶(mA写入器)、去甲基化酶(mA擦除器)和mA结合蛋白(mA读取器)调节这一动态可逆过程。在此,我们综述了mA修饰在决定病毒复制、形态发生、生命周期中的作用及其对疾病进展的贡献。为了揭示对抗病毒相关疾病的新方法,需要更好地了解病毒发病机制中的mA甲基化过程。