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http://purl.uniprot.org/citations/31915282http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31915282http://www.w3.org/2000/01/rdf-schema#comment"The virus-induced signaling adaptor (VISA) complex plays a critical role in the innate immune response to RNA viruses. However, the mechanism of VISA complex formation remains unclear. Here, we demonstrate that thioredoxin 2 (TRX2) interacts with VISA at mitochondria both in vivo and in vitro Knockdown and knockout of TRX2 enhanced the formation of the VISA-associated complex, as well as virus-triggered activation of interferon regulatory factor 3 (IRF3) and transcription of the interferon beta 1 (IFNB1) gene. TRX2 inhibits the formation of VISA aggregates by repressing reactive oxygen species (ROS) production, thereby disrupting the assembly of the VISA complex. Furthermore, our data suggest that the C93 residue of TRX2 is essential for inhibition of VISA aggregation, whereas the C283 residue of VISA is required for VISA aggregation. Collectively, these findings uncover a novel mechanism of TRX2 that negatively regulates VISA complex formation.IMPORTANCE The VISA-associated complex plays pivotal roles in inducing type I interferons (IFNs) and eliciting the innate antiviral response. Many host proteins are identified as VISA-associated-complex proteins, but how VISA complex formation is regulated by host proteins remains enigmatic. We identified the TRX2 protein as an important regulator of VISA complex formation. Knockout of TRX2 increases virus- or poly(I·C)-triggered induction of type I IFNs at the VISA level. Mechanistically, TRX2 inhibits the production of ROS at its C93 site, which impairs VISA aggregates at its C283 site, and subsequently impedes the assembly of the VISA complex. Our findings suggest that TRX2 plays an important role in the regulation of VISA complex assembly."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.org/dc/terms/identifier"doi:10.1128/jvi.01756-19"xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Liu X."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Li D."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Ren J."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Ru Y."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Zheng H."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/author"Yang W."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/name"J Virol"xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/pages"e01756-19"xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/title"Thioredoxin 2 Negatively Regulates Innate Immunity to RNA Viruses by Disrupting the Assembly of the Virus-Induced Signaling Adaptor Complex."xsd:string
http://purl.uniprot.org/citations/31915282http://purl.uniprot.org/core/volume"94"xsd:string
http://purl.uniprot.org/citations/31915282http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31915282
http://purl.uniprot.org/citations/31915282http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31915282
http://purl.uniprot.org/uniprot/#_A0A1S5UZH5-mappedCitation-31915282http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/#_B4DX69-mappedCitation-31915282http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/#_Q7Z434-mappedCitation-31915282http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/#_Q99757-mappedCitation-31915282http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/Q99757http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/Q7Z434http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/B4DX69http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31915282
http://purl.uniprot.org/uniprot/A0A1S5UZH5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31915282