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Structure of the Human cGAS-DNA Complex Reveals Enhanced Control of Immune Surveillance.

Cell | 2018

Cyclic GMP-AMP synthase (cGAS) recognition of cytosolic DNA is critical for immune responses to pathogen replication, cellular stress, and cancer. Existing structures of the mouse cGAS-DNA complex provide a model for enzyme activation but do not explain why human cGAS exhibits severely reduced levels of cyclic GMP-AMP (cGAMP) synthesis compared to other mammals. Here, we discover that enhanced DNA-length specificity restrains human cGAS activation. Using reconstitution of cGAMP signaling in bacteria, we mapped the determinant of human cGAS regulation to two amino acid substitutions in the DNA-binding surface. Human-specific substitutions are necessary and sufficient to direct preferential detection of long DNA. Crystal structures reveal why removal of human substitutions relaxes DNA-length specificity and explain how human-specific DNA interactions favor cGAS oligomerization. These results define how DNA-sensing in humans adapted for enhanced specificity and provide a model of the active human cGAS-DNA complex to enable structure-guided design of cGAS therapeutics.

Pubmed ID: 30007416 RIS Download

Associated grants

  • Agency: NCRR NIH HHS, United States
    Id: S10 RR029205
  • Agency: NIGMS NIH HHS, United States
    Id: P41 GM103403
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI018045
  • Agency: NCI NIH HHS, United States
    Id: R01 CA214608
  • Agency: NCI NIH HHS, United States
    Id: T32 CA207021

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