Two cGAS-like receptors induce antiviral immunity in Drosophila

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Holleufer, Andreas | Grønbjerg Winther, Kasper | Gad, Hans Henrik | Ai, Xianlong | Chen, Yuqiang | Li, Lihua | Wei, Ziming | Deng, Huimin | Liu, Jiyong | Frederiksen, Ninna Ahlmann | Simonsen, Bine | Andersen, Line Lykke | Kleigrewe, Karin | Dalskov, Louise | Pichlmair, Andreas | Cai, Hua | Imler, Jean-Luc | Hartmann, Rune

Edité par CCSD ; Nature Publishing Group -

International audience. In mammals, cyclic GMP–AMP (cGAMP) synthase (cGAS) produces the cyclic dinucleotide 2′3′-cGAMP in response to cytosolic DNA and this triggers an antiviral immune response. cGAS belongs to a large family of cGAS/DncV-like nucleotidyltransferases that is present in both prokaryotes1 and eukaryotes2–5. In bacteria, these enzymes synthesize a range of cyclic oligonucleotides and have recently emerged as important regulators of phage infections6–8. Here we identify two cGAS-like receptors (cGLRs) in the insect Drosophila melanogaster. We show that cGLR1 and cGLR2 activate Sting- and NF-κB-dependent antiviral immunity in response to infection with RNA or DNA viruses. cGLR1 is activated by double-stranded RNA to produce the cyclic dinucleotide 3′2′-cGAMP, whereas cGLR2 produces a combination of 2′3′-cGAMP and 3′2′-cGAMP in response to an as-yet-unidentified stimulus. Our data establish cGAS as the founding member of a family of receptors that sense different types of nucleic acids and trigger immunity through the production of cyclic dinucleotides beyond 2′3′-cGAMP.

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