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 PMID:27496731  

The AIM2-like Receptors Are Dispensable for the Interferon Response to Intracellular DNA.

Elizabeth E Gray | Damion Winship | Jessica M Snyder | Stephanie J Child | Adam P Geballe | Daniel B Stetson
Immunity | 2016

Detection of intracellular DNA triggers activation of the STING-dependent interferon-stimulatory DNA (ISD) pathway, which is essential for antiviral responses. Multiple DNA sensors have been proposed to activate this pathway, including AIM2-like receptors (ALRs). Whether the ALRs are essential for activation of this pathway remains unknown. To rigorously explore the function of ALRs, we generated mice lacking all 13 ALR genes. We found that ALRs are dispensable for the type I interferon (IFN) response to transfected DNA ligands, DNA virus infection, and lentivirus infection. We also found that ALRs do not contribute to autoimmune disease in the Trex1(-/-) mouse model of Aicardi-Goutières Syndrome. Finally, CRISPR-mediated disruption of the human AIM2-like receptor IFI16 in primary fibroblasts revealed that IFI16 is not essential for the IFN response to human cytomegalovirus infection. Our findings indicate that ALRs are dispensable for the ISD response and suggest that alternative functions for these receptors should be explored.

Pubmed ID: 27496731

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: R01 AI026672
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI084914
  • Agency: NIAID NIH HHS, United States
    Id: R56 AI113153
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001863

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International Mouse Phenotyping Consortium (IMPC) (tool)

RRID:SCR_006158

Center that produces knockout mice and carries out high-throughput phenotyping of each line in order to determine function of every gene in mouse genome. These mice will be preserved in repositories and made available to scientific community representing valuable resource for basic scientific research as well as generating new models for human diseases.

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