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Emerg Microbes Infect . Influenza NS1 Drives N6-Methyladenosine (m6A)-Mediated Autoregulation of Viral mRNA Splicing

tetano

Editor, Senior Moderator
Emerg Microbes Infect


. 2025 Oct 9:2572761.
doi: 10.1080/22221751.2025.2572761. Online ahead of print. Influenza NS1 Drives N[SUP]6[/SUP]-Methyladenosine (m[SUP]6[/SUP]A)-Mediated Autoregulation of Viral mRNA Splicing

Yingyin Liao[SUP] 1 2 3 [/SUP], Jiayan Liu[SUP] 1 2 3 [/SUP], Pui Wang[SUP] 1 2 [/SUP], Bobo Wing-Yee Mok[SUP] 1 2 [/SUP], Honglin Chen[SUP] 1 2 3 [/SUP]



Affiliations
Free article Abstract

Influenza A virus replication requires precise balance between unspliced and spliced viral mRNAs. However, the regulatory mechanisms governing viral mRNA splicing remain poorly understood. In this study, we uncover an epigenetic strategy whereby the viral NS1 protein autoregulates its own mRNA splicing via N[SUP]6[/SUP]-methyladenosine (m[SUP]6[/SUP]A) modification. Specifically, m[SUP]6[/SUP]A modification at residue A385 on NS mRNA recruits the m[SUP]6[/SUP]A reader YTHDC1, which competitively inhibits the splicing factor SRSF3 from binding proximal sites. Importantly, we demonstrate that the A385 m[SUP]6[/SUP]A site is conserved and essential for splicing regulation in the NS segment across human and avian influenza strains. Our findings suggest that, by dynamically modulating m[SUP]6[/SUP]A levels, NS1 fine-tunes viral mRNA processing to enhance replication efficiency. This work elucidates NS1 as an m[SUP]6[/SUP]A-driven splicing regulator and identifies this conserved m[SUP]6[/SUP]A site as a potential target for broad-spectrum antiviral development.

Keywords: NS1; epitranscriptomics; influenza virus; m6A modification; viral mRNA splicing.

 
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