FB2025_01 , released February 20, 2025
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Citation
Zhang, L., Xu, W., Gao, X., Li, W., Qi, S., Guo, D., Ajayi, O.E., Ding, S.W., Wu, Q. (2020). lncRNA Sensing of a Viral Suppressor of RNAi Activates Non-canonical Innate Immune Signaling in Drosophila.  Cell Host Microbe 27(1): 115--128.e8.
FlyBase ID
FBrf0244474
Publication Type
Research paper
Abstract
Antiviral immunity in insects is mediated by the RNA interference (RNAi) pathway. Viruses evade antiviral RNAi by expressing virulence factors known as viral suppressors of RNAi (VSR). Here, we report the identification of VINR, a Drosophila VSR-interacting long non-coding (lnc) RNA that activates non-canonical innate immune signaling upon detection of the dsRNA-binding VSR of Drosophila C virus (DCV). VINR is required for the induction of antimicrobial peptide (AMP) genes but dispensable for antiviral RNAi. VINR functions by preventing the ubiquitin proteasome-dependent degradation of Cactin, a coiled-coil and arginine-serine-rich domain-containing protein that regulates a non-cannonical antimicrobial pathway for AMP induction. CRISPR-Cas9 knockout of VINR in Drosophila cells enhances DCV replication independently of antiviral RNAi, and VINR-knockout adult flies exhibit enhanced disease susceptibility to DCV and bacteria. Our findings reveal a counter counter-defense strategy activated by a lncRNA in response to the viral suppression of the primary antiviral RNAi immunity.
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PubMed Central ID
Related Publication(s)
Personal communication to FlyBase

Location data for lncRNA:Vinr[KO].
Zhang and Wu, 2020.3.11, Location data for lncRNA:Vinr[KO]. [FBrf0245090]

Note

Countering Counter-Defense to Antiviral RNAi.
Betting and Van Rij, 2020, Trends Microbiol. 28(8): 600--602 [FBrf0246234]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell Host Microbe
    Title
    Cell Host & Microbe
    Publication Year
    2007--
    ISBN/ISSN
    1931-3128 1934-6069
    Data From Reference
    Alleles (1)
    Genes (30)
    Physical Interactions (6)
    Sequence Features (3)
    Cell Lines (1)