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Inefficient splicing of segment 7 and 8 mRNAs is an inherent property of influenza virus A/Brevig Mission/1918/1 (H1N1) that causes elevated expression of NS1 protein.
Department of Laboratory Medicine, Section of Medical Microbiology, Lund University, Lund, Sweden; Department of Medical Biochemistry and Microbiology, Biomedical Centre, Uppsala University, Uppsala, Sweden .
Department of Medical Biochemistry and Microbiology, Department of Laboratory Medicine, Section of Medical Microbiology, Lund University, Lund, Sweden; Department of Medical Biochemistry and Microbiology, Biomedical Centre, Uppsala University, Uppsala, Sweden .ORCID iD: 0000-0003-0902-508X
Department of Medical Biochemistry and Microbiology, Department of Laboratory Medicine, Section of Medical Microbiology, Lund University, Lund, Sweden; Department of Medical Biochemistry and Microbiology, Biomedical Centre, Uppsala University, Uppsala, Sweden .
Department of Medical Biochemistry and Microbiology, Department of Laboratory Medicine, Section of Medical Microbiology, Lund University, Lund, Sweden; Department of Medical Biochemistry and Microbiology, Biomedical Centre, Uppsala University, Uppsala, Sweden .
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2012 (English)In: Virology, ISSN 0042-6822, E-ISSN 1096-0341, Vol. 422, no 1, p. 46-58Article in journal (Refereed) Published
Abstract [en]

Influenza A virus encodes two segments (7 and 8) that produce mRNAs that can be spliced. We have investigated if naturally occurring sequence polymorphisms in the influenza A virus family affects splicing of these viral mRNAs, as that could potentially alter the NS1/NS2- and/or M1/M2-protein ratios. We compared splicing efficiency of segment 7 and 8 mRNAs of A/Brevig Mission/1918/1 (H1N1) and A/Netherlands/178/95 (H3N2), as well as various H5N1 avian strains. Results revealed that both segment 7 and 8 mRNAs of A/Brevig Mission/1918/1 (H1N1) were inefficiently spliced compared to other influenza virus segment 7 and 8 mRNAs. This resulted in production of higher levels of functional NS1 protein, which could potentially contribute to the pathogenic properties of the A/Brevig Mission/1918/1 (H1N1). We also show that A/Brevig Mission/1918/1 (H1N1) segment 8 mRNAs responded differently to overexpression of SR proteins than A/Netherlands/178/95 (H3N2).

Place, publisher, year, edition, pages
2012. Vol. 422, no 1, p. 46-58
Keywords [en]
ASF/SF2; Influenza; NS1; Polyadenylation; Spanish flu; Splicing; SR proteins; SRp30c; SRp40
National Category
Basic Medicine
Identifiers
URN: urn:nbn:se:oru:diva-41995DOI: 10.1016/j.virol.2011.10.004ISI: 000297902300006PubMedID: 22036312Scopus ID: 2-s2.0-82355190150OAI: oai:DiVA.org:oru-41995DiVA, id: diva2:792890
Funder
Swedish Research CouncilAFA Insurance
Note

Funding Agency:

European Commission 201607 (RNAFLU)

Available from: 2015-03-05 Created: 2015-01-16 Last updated: 2018-05-14Bibliographically approved

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Abdurahman, Samir

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