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TitleStructural mechanism of cGAS inhibition by the nucleosome.
Journal, issue, pagesNature, Vol. 587, Issue 7835, Page 668-672, Year 2020
Publish dateSep 10, 2020
AuthorsGanesh R Pathare / Alexiane Decout / Selene Glück / Simone Cavadini / Kristina Makasheva / Ruud Hovius / Georg Kempf / Joscha Weiss / Zuzanna Kozicka / Baptiste Guey / Pauline Melenec / Beat Fierz / Nicolas H Thomä / Andrea Ablasser /
PubMed AbstractThe DNA sensor cyclic GMP-AMP synthase (cGAS) initiates innate immune responses following microbial infection, cellular stress and cancer. Upon activation by double-stranded DNA, cytosolic cGAS ...The DNA sensor cyclic GMP-AMP synthase (cGAS) initiates innate immune responses following microbial infection, cellular stress and cancer. Upon activation by double-stranded DNA, cytosolic cGAS produces 2'3' cGMP-AMP, which triggers the induction of inflammatory cytokines and type I interferons . cGAS is also present inside the cell nucleus, which is replete with genomic DNA, where chromatin has been implicated in restricting its enzymatic activity. 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.
External linksNature / PubMed:32911482
MethodsEM (single particle)
Resolution3.15 - 5.1 Å
Structure data

10694

6y5d

EMDB-10694, PDB-6y5d:
Structure of human cGAS (K394E) bound to the nucleosome
Method: EM (single particle) / Resolution: 4.1 Å

10695

6y5e

EMDB-10695, PDB-6y5e:
Structure of human cGAS (K394E) bound to the nucleosome (focused refinement of cGAS-NCP subcomplex)
Method: EM (single particle) / Resolution: 3.15 Å

EMDB-11005:
Structure of human cGAS bound to the nucleosome (focused refinement of cGAS-NCP subcomplex)
Method: EM (single particle) / Resolution: 4.7 Å

EMDB-11006:
Structure of human cGAS bound to the nucleosome
Method: EM (single particle) / Resolution: 5.1 Å

Chemicals

ChemComp-PTD:
PENTANEDIAL

ChemComp-ZN:
Unknown entry

Source
  • homo sapiens (human)
KeywordsIMMUNE SYSTEM / cGAS / STING / Nucleosome / Innate Immunity / cGMP-AMP

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