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pubmed, article, google, scholar, cas, central, viral, data, nature, rna, elegans, orv, infection, supplementary, figure, source, caenorhabditis, cde, cell, expression, antiviral, access, biology, cambridge, mrna, stress, sensor, molecular, genome, independent, uridylation, university, content, viruses, pen, virus, days, research, mutants, gfp, information, domenico, miska, rnas, gene, type, biol, bioinformatics, cookies, structural,

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Questions {❓}

• Is anti-viral defence the evolutionary origin of mRNA turnover?

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         headline:Terminal uridylyltransferases target RNA viruses as part of the innate immune system
         description:RNA viruses are a major threat to animals and plants. RNA interference (RNAi) and the interferon response provide innate antiviral defense against RNA viruses. Here, we performed a large-scale screen using Caenorhabditis elegans and its natural pathogen the Orsay virus (OrV), and we identified cde-1 as important for antiviral defense. CDE-1 is a homolog of the mammalian TUT4 and TUT7 terminal uridylyltransferases (collectively called TUT4(7)); its catalytic activity is required for its antiviral function. CDE-1 uridylates the 3ʹ end of the OrV RNA genome and promotes its degradation in a manner independent of the RNAi pathway. Likewise, TUT4(7) enzymes uridylate influenza A virus (IAV) mRNAs in mammalian cells. Deletion of TUT4(7) leads to increased IAV mRNA and protein levels. Collectively, these data implicate 3ʹ-terminal uridylation of viral RNAs as a conserved antiviral defense mechanism. A screen for C. elegans antiviral-defense genes identifies a homolog of the mammalian TUT4(7) terminal uridylyltransferase genes and leads to the discovery of 3′-terminal uridylation of viral RNAs as a conserved antiviral defense mechanism.
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      headline:Terminal uridylyltransferases target RNA viruses as part of the innate immune system
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