The mechanism of double-stranded DNA sensing through the cGAS-STING pathway

Cytokine Growth Factor Rev. 2014 Dec;25(6):641-8. doi: 10.1016/j.cytogfr.2014.06.006. Epub 2014 Jun 22.

Abstract

Microbial nucleic acids induce potent innate immune responses by stimulating the expression of type I interferons. Cyclic GMP-AMP synthase (cGAS) is a cytosolic dsDNA sensor mediating the innate immunity to microbial DNA. cGAS is activated by dsDNA and catalyze the synthesis of a cyclic dinucleotide cGAMP with 2',5' and 3',5'phosphodiester linkages. cGAMP binds to the adaptor STING located on the endoplasmic reticulum membrane and mediates the recruitment and activation of the protein kinase TBK1 and transcription factor IRF3. Phosphorylated IRF3 translocates to the nucleus and initiates the transcription of the IFN-β gene. The crystal structures of cGAS and its complex with dsDNA, STING and its complex with various cyclic dinucleotides have been determined recently. Here we summarize the results from these structural studies and provide an overview about the mechanism of cGAS activation by dsDNA, the catalytic mechanism of cGAS, and the structural basis of STING activation by cGAMP.

Keywords: Cyclic dinucleotides; Innate immunity; Nucleic acids; Pattern recognition receptors; Type I interferons.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Active Transport, Cell Nucleus / genetics
  • Active Transport, Cell Nucleus / immunology
  • Animals
  • Cell Nucleus / genetics
  • Cell Nucleus / immunology
  • DNA / genetics
  • DNA / immunology*
  • Endoplasmic Reticulum / genetics
  • Endoplasmic Reticulum / immunology
  • Humans
  • Interferon Regulatory Factor-3 / genetics
  • Interferon Regulatory Factor-3 / immunology
  • Interferon-beta / genetics
  • Interferon-beta / immunology
  • Intracellular Membranes / immunology
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology*
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / immunology*
  • Phosphorylation / genetics
  • Phosphorylation / immunology
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / immunology
  • Signal Transduction / genetics
  • Signal Transduction / immunology*
  • Transcriptional Activation / genetics
  • Transcriptional Activation / immunology

Substances

  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • Membrane Proteins
  • STING1 protein, human
  • Interferon-beta
  • DNA
  • Protein Serine-Threonine Kinases
  • TBK1 protein, human
  • Nucleotidyltransferases
  • cGAS protein, human