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FAS-associated factor-1 positively regulates type I interferon response to RNA virus infection by targeting NLRX1
- Source :
- PLoS Pathogens, Vol 13, Iss 5, p e1006398 (2017), PLOS PATHOGENS(13): 5, PLoS Pathogens
- Publication Year :
- 2017
- Publisher :
- Public Library of Science (PLoS), 2017.
-
Abstract
- FAS-associated factor-1 (FAF1) is a component of the death-inducing signaling complex involved in Fas-mediated apoptosis. It regulates NF-kappa B activity, ubiquitination, and proteasomal degradation. Here, we found that FAF1 positively regulates the type I interferon pathway. FAF1(gt/gt) mice, which deficient in FAF1, and FAF1 knockdown immune cells were highly susceptible to RNA virus infection and showed low levels of inflammatory cytokines and type I interferon (IFN) production. FAF1 was bound competitively to NLRX1 and positively regulated type I IFN signaling by interfering with the interaction between NLRX1 and MAVS, thereby freeing MAVS to bind RIG-I, which switched on the MAVS-RIG-I-mediated antiviral signaling cascade. These results highlight a critical role of FAF1 in antiviral responses against RNA virus infection.
- Subjects :
- 0301 basic medicine
Male
lcsh:Immunologic diseases. Allergy
Immunology
Biology
Microbiology
Proinflammatory cytokine
Mitochondrial Proteins
03 medical and health sciences
Mice
RNA Virus Infections
RNA interference
Interferon
Virology
Genetics
medicine
Animals
Humans
RNA Viruses
Molecular Biology
lcsh:QH301-705.5
Adaptor Proteins, Signal Transducing
Mice, Knockout
Gene knockdown
030102 biochemistry & molecular biology
Macrophages
Intracellular Signaling Peptides and Proteins
NF-kappa B
Correction
RNA virus
biology.organism_classification
Molecular biology
Cell biology
Mice, Inbred C57BL
030104 developmental biology
lcsh:Biology (General)
Apoptosis
Interferon Type I
Parasitology
Female
RNA extraction
Apoptosis Regulatory Proteins
Carrier Proteins
lcsh:RC581-607
Interferon type I
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 15537374 and 15537366
- Volume :
- 13
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- PLoS Pathogens
- Accession number :
- edsair.doi.dedup.....7d15e7d27251064ee5a662f81b42d36a