cGLRs are a diverse family of pattern recognition receptors in innate immunity.
Li, Y., Slavik, K.M., Toyoda, H.C., Morehouse, B.R., de Oliveira Mann, C.C., Elek, A., Levy, S., Wang, Z., Mears, K.S., Liu, J., Kashin, D., Guo, X., Mass, T., Sebe-Pedros, A., Schwede, F., Kranzusch, P.J.(2023) Cell 186: 3261-3276.e20
- PubMed: 37379839 
- DOI: https://doi.org/10.1016/j.cell.2023.05.038
- Primary Citation of Related Structures:  
8EFM, 8EFN, 8GJW, 8GJX, 8GJY, 8GJZ - PubMed Abstract: 
Cyclic GMP-AMP synthase (cGAS) is an enzyme in human cells that controls an immune response to cytosolic DNA. Upon binding DNA, cGAS synthesizes a nucleotide signal 2'3'-cGAMP that activates STING-dependent downstream immunity. Here, we discover that cGAS-like receptors (cGLRs) constitute a major family of pattern recognition receptors in innate immunity. Building on recent analysis in Drosophila, we identify >3,000 cGLRs present in nearly all metazoan phyla. A forward biochemical screening of 150 animal cGLRs reveals a conserved mechanism of signaling including response to dsDNA and dsRNA ligands and synthesis of isomers of the nucleotide signals cGAMP, c-UMP-AMP, and c-di-AMP. Combining structural biology and in?vivo analysis in coral and oyster animals, we explain how synthesis of distinct nucleotide signals enables cells to control discrete cGLR-STING signaling pathways. Our results reveal cGLRs as a widespread family of pattern recognition receptors and establish molecular rules that govern nucleotide signaling in animal immunity.
Organizational Affiliation: 
Department of Microbiology, Harvard Medical School, Boston, MA 02115, USA; Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02115, USA; Parker Institute for Cancer Immunotherapy at Dana-Farber Cancer Institute, Boston, MA 02115, USA.