SNAP output for PDB entry 6y5e [SNAP web server]

PDB-id

6y5e; SNAP-derived features in text and JSON formats; DNAproDB

Class

immune system

Method

cryo-EM (3.15 Å)

Summary

Structure of human cgas (k394e) bound to the nucleosome (focused refinement of cgas-ncp subcomplex)

Reference

Pathare GR, Decout A, Gluck S, Cavadini S, Makasheva K, Hovius R, Kempf G, Weiss J, Kozicka Z, Guey B, Melenec P, Fierz B, Thoma NH, Ablasser A (2020): "Structural mechanism of cGAS inhibition by the nucleosome." Nature, 587, 668-672. doi: 10.1038/s41586-020-2750-6.

Abstract

The DNA sensor cyclic GMP-AMP synthase (cGAS) initiates innate immune responses following microbial infection, cellular stress and cancer₁. Upon activation by double-stranded DNA, cytosolic cGAS produces 2'3' cGMP-AMP, which triggers the induction of inflammatory cytokines and type I interferons _2-7. cGAS is also present inside the cell nucleus, which is replete with genomic DNA₈, where chromatin has been implicated in restricting its enzymatic activity₉. However, the structural basis for inhibition of cGAS by chromatin remains unknown. Here we present the cryo-electron microscopy structure of human cGAS bound to nucleosomes. cGAS makes extensive contacts with both the acidic patch of the histone H2A-H2B heterodimer and nucleosomal DNA. The structural and complementary biochemical analysis also find cGAS engaged to a second nucleosome in trans. Mechanistically, binding of the nucleosome locks cGAS into a monomeric state, in which steric hindrance suppresses spurious activation by genomic DNA. We find that mutations to the cGAS-acidic patch interface are sufficient to abolish the inhibitory effect of nucleosomes in vitro and to unleash the activity of cGAS on genomic DNA in living cells. Our work uncovers the structural basis of the interaction between cGAS and chromatin and details a mechanism that permits self-non-self discrimination of genomic DNA by cGAS.