Two cGAS-like receptors induce antiviral immunity in Drosophila.
Andreas HolleuferKasper Grønbjerg WintherHans Henrik GadXianlong AiYuqiang ChenLihua LiZiming WeiHuimin DengJiyong LiuNinna Ahlmann FrederiksenBine SimonsenLine Lykke AndersenKarin KleigreweLouise DalskovAndreas PichlmairHua CaiJean-Luc ImlerRune HartmannPublished in: Nature (2021)
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.
Keyphrases
- nucleic acid
- immune response
- drosophila melanogaster
- circulating tumor
- cell free
- signaling pathway
- oxidative stress
- electronic health record
- transcription factor
- machine learning
- inflammatory response
- staphylococcus aureus
- artificial intelligence
- protein kinase
- pi k akt
- cystic fibrosis
- cell proliferation
- nuclear factor