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About:
Non-degradative Role of Atg5-Atg12/Atg16L1 Autophagy Protein Complex in Antiviral Activity of Interferon gamma
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Non-degradative Role of Atg5-Atg12/Atg16L1 Autophagy Protein Complex in Antiviral Activity of Interferon gamma
Creator
Zhang, Lei
Hwang, Seungmin
Diamond, Michael
Shrestha, Bimmi
Duan, Erning
Goel, Gautam
Xavier, Ramnik
Dani, Adish
Lopez-Otin, Carlos
Bruinsma, Monique
Green, Kim
Maloney, Nicole
Sosnovtsev, Stanislav
Thackray, Larissa
Virgin, Herbert
topic
covid:2bac9f0274777b7647eb51522a6ed32d12647a7a#this
Source
Elsevier; Medline; PMC
abstract
Host resistance to viral infection requires Type-I (α/β) and -II (γ) interferon (IFN) production. Another important defense mechanism is the degradative activity of macroautophagy (herein autophagy), mediated by the coordinated action of evolutionarily conserved autophagy proteins (Atg). We show that the Atg5-Atg12/Atg16L1 protein complex, whose prior known function is in autophagosome formation, is required for IFNγ-mediated host defense against murine norovirus (MNV) infection. Importantly, the direct antiviral activity of IFNγ against MNV in macrophages required Atg5-Atg12, Atg7, and Atg16L1, but not induction of autophagy, the degradative activity of lysosomal proteases, fusion of autophagosomes and lysosomes, or the Atg8 processing protein Atg4B. IFNγ, via Atg5-Atg12/Atg16L1, inhibited formation of the membranous cytoplasmic MNV replication complex, where Atg16L1 localized. Thus, the Atg5-Atg12/Atg16L1 complex performs a pivotal, nondegradative role in IFNγ-mediated antiviral defense, establishing that multicellular organisms have evolved to use portions of the autophagy pathway machinery in a cassette-like fashion for host defense.
has issue date
2012-04-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.chom.2012.03.002
bibo:pmid
22520467
has license
hybrid-oa
sha1sum (hex)
2bac9f0274777b7647eb51522a6ed32d12647a7a
schema:url
https://doi.org/10.1016/j.chom.2012.03.002
resource representing a document's title
Non-degradative Role of Atg5-Atg12/Atg16L1 Autophagy Protein Complex in Antiviral Activity of Interferon gamma
has PubMed Central identifier
PMC3348177
has PubMed identifier
22520467
schema:publication
Cell Host & Microbe
resource representing a document's body
covid:2bac9f0274777b7647eb51522a6ed32d12647a7a#body_text
is
http://vocab.deri.ie/void#inDataset
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proxy:http/ns.inria.fr/covid19/2bac9f0274777b7647eb51522a6ed32d12647a7a
is
schema:about
of
named entity 'INTERFERON GAMMA'
named entity 'Atg5'
named entity 'Atg16L1'
named entity 'MICROBE'
named entity 'ATG16L1'
named entity 'THE JACKSON LABORATORY'
named entity 'CRE RECOMBINASE'
named entity 'ANTIVIRAL ACTIVITY'
named entity 'ROLE'
named entity 'USED'
named entity 'PURCHASED'
named entity 'LYSOZYME'
named entity 'MIXED'
named entity 'LOCUS'
named entity '129'
named entity 'CELL'
named entity 'ATG12'
named entity 'CONSISTENT'
named entity 'DIFFERENT'
named entity 'C57BL'
named entity 'INFORMATION'
named entity 'HOST'
named entity 'PROTEIN COMPLEX'
named entity 'OBSERVED'
named entity 'PHENOTYPES'
named entity 'ATG5'
named entity 'SUPPLEMENTAL'
named entity 'ATG5'
named entity 'AUTOPHAGY'
named entity 'FIGURES'
named entity 'STUDY'
named entity 'MICE'
named entity 'mice'
named entity 'mice'
named entity 'Antiviral'
named entity 'Cre recombinase'
named entity 'phenotypes'
named entity 'mice'
named entity 'Atg16L1'
named entity 'Autophagy'
named entity 'Astigmatism'
named entity 'ATP'
named entity 'anti-FLAG'
named entity 'Atg5'
named entity 'glycolysis'
named entity 'loading control'
named entity 'MEF'
named entity 'serum'
named entity 'autophagy'
named entity 'vector'
named entity 'Atg16L1'
named entity 'RNase protection assay'
named entity 'IgG'
named entity 'western blot'
named entity 'SEM'
named entity 'macrophages'
named entity 'western blot'
named entity 'Switzerland'
named entity 'western blot'
named entity 'Cycloheximide'
named entity 'loading control'
named entity 'transfected'
named entity 'ATP'
named entity 'epifluorescence'
named entity 'cycloheximide'
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