| Literature DB >> 34261128 |
Andreas Holleufer1, Kasper Grønbjerg Winther2, Hans Henrik Gad1, Xianlong Ai3, Yuqiang Chen3, Lihua Li3, Ziming Wei3, Huimin Deng3, Jiyong Liu3, Ninna Ahlmann Frederiksen1, Bine Simonsen1, Line Lykke Andersen4, Karin Kleigrewe5, Louise Dalskov1, Andreas Pichlmair4,6, Hua Cai7, Jean-Luc Imler8,9, Rune Hartmann10.
Abstract
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.Entities:
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Year: 2021 PMID: 34261128 DOI: 10.1038/s41586-021-03800-z
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962