Structural analysis of 3’UTRs in insect flaviviruses reveals novel determinants of sfRNA biogenesis and provides new insights into flavivirus evolution

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作者
Andrii Slonchak
Rhys Parry
Brody Pullinger
Julian D. J. Sng
Xiaohui Wang
Teresa F. Buck
Francisco J. Torres
Jessica J. Harrison
Agathe M. G. Colmant
Jody Hobson-Peters
Roy A. Hall
Andrew Tuplin
Alexander A. Khromykh
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[1] University of Queensland,School of Chemistry and Molecular Biosciences
[2] Global Virus Network Centre of Excellence,Australian Infectious Diseases Research Centre
[3] University of Leeds,School of Molecular and Cellular Biology
[4] University of Lübeck,Institute for Medical and Marine Biotechnology
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Subgenomic flaviviral RNAs (sfRNAs) are virus-derived noncoding RNAs produced by pathogenic mosquito-borne flaviviruses (MBF) to counteract the host antiviral response. To date, the ability of non-pathogenic flaviviruses to produce and utilise sfRNAs remains largely unexplored, and it is unclear what role XRN1 resistance plays in flavivirus evolution and host adaptation. Herein the production of sfRNAs by several insect-specific flaviviruses (ISFs) that replicate exclusively in mosquitoes is shown, and the secondary structures of their complete 3’UTRs are determined. The xrRNAs responsible for the biogenesis of ISF sfRNAs are also identified, and the role of these sfRNAs in virus replication is demonstrated. We demonstrate that 3’UTRs of all classical ISFs, except Anopheles spp-asscoaited viruses, and of the dual-host associated ISF Binjari virus contain duplicated xrRNAs. We also reveal novel structural elements in the 3’UTRs of dual host-associated and Anopheles-associated classical ISFs. Structure-based phylogenetic analysis demonstrates that xrRNAs identified in Anopheles spp-associated ISF are likely ancestral to xrRNAs of ISFs and MBFs. In addition, our data provide evidence that duplicated xrRNAs are selected in the evolution of flaviviruses to provide functional redundancy, which preserves the production of sfRNAs if one of the structures is disabled by mutations or misfolding.
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