N6-Methyladenosine and Viral Infection

N 6 -methyladenosine (m 6 A), as a dynamic posttranscriptional RNA modification, recently gave rise to the field of viral epitranscriptomics. The interaction between virus and host is affected by m 6 A. Multiple m 6 A-modified viral RNAs have been observed. The epitranscriptome of m 6 A in host cell...

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Published inFrontiers in microbiology Vol. 10; p. 417
Main Authors Dang, Wei, Xie, Yan, Cao, Pengfei, Xin, Shuyu, Wang, Jia, Li, Shen, Li, Yanling, Lu, Jianhong
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 05.03.2019
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Summary:N 6 -methyladenosine (m 6 A), as a dynamic posttranscriptional RNA modification, recently gave rise to the field of viral epitranscriptomics. The interaction between virus and host is affected by m 6 A. Multiple m 6 A-modified viral RNAs have been observed. The epitranscriptome of m 6 A in host cells are altered after viral infection. The expression of viral genes, the replication of virus and the generation of progeny virions are influenced by m 6 A modifications in viral RNAs during virus infection. Meanwhile, the decorations of m 6 A in host mRNAs can make viral infections more likely to happen or can enhance the resistance of host to virus infection. However, the mechanism of m 6 A regulation in viral infection and host immune response has not been thoroughly elucidated to date. With the development of sequencing-based biotechnologies, transcriptome-wide mapping of m 6 A in viruses has been achieved, laying the foundation for expanding its functions and corresponding mechanisms. In this report, we summarize the positive and negative effects of m 6 A in distinct viral infection. Given the increasingly important roles of m 6 A in diverse viruses, m 6 A represents a novel potential target for antiviral therapy.
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Reviewed by: Hao Lin, University of Electronic Science and Technology of China, China; Takashi Irie, Hiroshima University, Japan
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
Edited by: Herman W. Favoreel, Ghent University, Belgium
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2019.00417