The miR-302 cluster-IRFs-IRF1AS axis regulates influenza A virus replication in a species-specific manner

Non-coding RNAs are crucial orchestrators in the intricate dance between viruses and host cells, among which the expression and function of enhancer RNAs (eRNAs) during influenza virus infection remain largely unexplored. This study utilized whole transcriptome high-throughput sequencing to investigate the molecular mechanisms underpinning the species-specific regulation of influenza virus replication by the miR-302 cluster-IRFs-IRF1AS axis both in vivo and in vitro. Mechanistically, the CTNNB1-induced miR-302 cluster targeted various interferon regulatory factors (mainly IRF1 and IRF2) with varying affinities and silencing efficiencies, except for miR-302e and miR-302f. Furthermore, miR-302 cluster-IRFs triggered the induction of interferon-induced hub genes and hub lncRNAs defined through weighted gene co-expression network analysis. Importantly, the intricate interplay between IRFs, direct targets of the miR-302 cluster, and IRF1AS, an indirect target, in terms of gene loci and transcriptional regulation reveals a crosstalk in the miR-302 cluster-IRFs-IRF1AS axis. That is, on the one hand, IRF1 and IRF7 bind to the promoter of IRF1AS to promote the transcription of eRNAs. On the other hand, IRF1AS functions as an enhancer cluster that orchestrates and cis-regulates the transcription of IRF1, thereby rapidly amplifying the antiviral immune response initiated by miR-302 cluster-IRFs. In conclusion, we have unveiled a novel regulatory network governed by the miR-302 cluster-IRFs-IRF1AS, offering fresh perspectives on immune regulatory mechanisms.

Non-coding RNAs play a crucial role in regulating the three-dimensional structure of chromatin. They influence gene expression through various mechanisms and thereby contribute to the onset and progression of influenza A virus pathogenicity. Our comprehensive whole transcriptome sequencing analysis reveals a novel finding: the species-specific regulation of influenza virus replication by the miR-302 cluster-IRFs-IRF1AS axis. Our findings indicate that the miR-302 cluster-IRFs axis facilitates the transcription of key hub genes and hub lncRNAs, most of which significantly inhibit influenza virus replication. Notably, the downstream IRF1AS assembles into an enhancer cluster, orchestrating and cis-regulating the transcription of IRF1 to activate the interferon system. This investigation enhances our understanding of the regulatory network underlying viral infections and offers novel insights into immune regulatory mechanisms.