InnateDB: Systems Biology of the Innate Immune Response

Bos taurus Gene: BT.45349

Summary

InnateDB Gene

IDBG-640031.3

Last Modified

2014-10-13 [Report errors or provide feedback]

Gene Symbol

BT.45349

Gene Name

mitochondrial antiviral-signaling protein

Synonyms

VISA

Species

Bos taurus

Ensembl Gene

ENSBTAG00000013545

Encoded Proteins

IDBP-692233

mitochondrial antiviral-signaling protein

Protein Structure

Useful resources

Stemformatics EHFPI ImmGen

InnateDB Annotation from Orthologs

Summary

PMID 19036819

[Homo sapiens] MAVS oligomer is essential in the formation of a multiprotein membrane-associated signalling complex that enables downstream activation of IRF3 and NF-kappaB in antiviral innate immunity.

PMID 16177806

[Homo sapiens] MAVS is a caspase recruitment domain (CARD)-containing adaptor protein that interacts with DDX58 (RIG-I) and recruits CHUK (IKKalpha), IKBKB (IKKbeta) and IKBKE (IKKepsilon) kinases by means of its C-terminal region, leading to the activation of NF-kappaB and IRF3.

PMID 16125763

[Homo sapiens] MAVS is an adaptor protein that contains an N-terminal caspase recruitment domain (CARD)-like domain and a C-terminal transmembrane domain, both of which are essential for MAVS signalling, while the transmembrane domain also targets MAVS to the mitochondria.

PMID 20032188

[Homo sapiens] MAVS facilitates cell death by disrupting the mitochondrial membrane potential and by activating caspases.

PMID 20140199

[Homo sapiens] MAVS-dependent RIG-I-like receptor (RLR) signalling regulates the quantity, quality, and balance of the immune response to West Nile virus (WNV) infection.

PMID 20451243

[Homo sapiens] MAVS in peroxisomes induces a rapid interferon-independent expression of defence factors that provide short-term protection, whereas mitochondrial MAVS activates an interferon-dependent signalling pathway with delayed kinetics, which amplifies and stabilizes the antiviral response.

PMID 20554965

[Homo sapiens] MAVS interacts with hepatitis B virus X protein and this promotes the degradation of MAVS via Lys(136) ubiquitination, preventing the induction of IFN-beta.

PMID 20661427

[Homo sapiens] MAVS (IPS-1) interacts with MFN1 upon virus-infection or 5'ppp-RNA activation through redistribution of MAVS to form speck-like aggregates in cells.

PMID 20699220

[Homo sapiens] MAVS (IPS1) plays an important role in regulating the host anti-viral response by binding to viral polymerase and inhibiting IFN-beta production.

PMID 21110072

[Homo sapiens] MAVS negatively regulates the stability of voltage-dependent anion channel 1 (VDAC1) and thereby inhibits apoptosis in the response to release of cytochrome c.

PMID 21454965

[Homo sapiens] The MAVS signalling pathway in non-myeloid cells is crucial for dsRNA-mediated natural killer cell activation. (Demonstrated in murine model)

PMID 22844514

[Homo sapiens] Tyrosine phosphorylation of MAVS at amino acid residue Tyr9 is critical for the induction of IFNB signalling.

PMID 23028806

[Homo sapiens] MAVS mRNA is degraded in response to foreign RNA and poly(I:C) to suppress hyper-immune reaction in late-phase antiviral signalling.

PMID 23582325

[Homo sapiens] MAVS is required for optimal NLRP3 inflammasome activity by mediating mitochondrial recruitment of NLRP3.

PMID 23555247

[Homo sapiens] MAVS is targeted by enterovirus protease to evade antiviral immunity.

PMID 23951545

[Homo sapiens] The binding of MAVS to Traf2, Traf5, and Traf6 is dependent on virus infection and MAVS polymerization. The TRAF proteins promote ubiquitination that recruits IKBKG binding to the MAVS signalling complex.

PMID 24651600

[Homo sapiens] Upon viral infection, MAVS recruits MKK7 onto mitochondria, leading to the induction of apoptosis by MAP2K7 activated MAPK9

PMID 25463536

[Homo sapiens] Macrocyclic NS3-4A resistance-associated amino acid variants (RAVs) with substitutions at residue D168 of the hepatitis C virus protease result in an increased capacity of NS3-4A to cleave MAVS and suppress IFNB1 induction.

PMID 25816776

[Homo sapiens] RNA cleavage products, catalyzed by RNASEL, bind to DHX33 to facilitate the formation of a complex with MAVS and NLRP3 during viral infection.

PMID 27213432

[Homo sapiens] HACE1 plays an inhibitory role in virus-induced signalling by disrupting the MAVS-TRAF3 complex.

PMID 26246171

[Homo sapiens] MARCH5 modulates MAVS-mediated antiviral signalling, preventing excessive immune reactions.

PMID 26385923

[Homo sapiens] MAVS directly interacts with TRAF6 through its potential TRAF6-binding motif 2.

PMID 21454965

[Mus musculus] The Mavs signalling pathway in non-myeloid cells is crucial for dsRNA-mediated natural killer cell activation.

PMID 22844514

[Mus musculus] Tyrosine phosphorylation of Mavs at amino acid residue Tyr9 is critical for the induction of Ifnb signalling. (Demonstrated in human)

PMID 23499490

[Mus musculus] Upon infection with encephalitic Bunyavirus, RIG-I/MAVS signalling activates SARM1 to mediate neuronal cell death.

PMID 23754752

[Mus musculus] MAVS binds to VDAC1 to trigger viral-induced apoptosis.

PMID 24362933

[Mus musculus] Plasmodium RNA is a pathogen-associated molecular pattern (PAMP) capable of activating a type I IFN response via the cytosolic pattern recognition receptors Ifih1 and Mavs, as well as via transcription factors Irf3 and Irf7.

PMID 26079065

[Mus musculus] Antiviral response to rotavirus in infected macrophages is fully Mavs-dependent.

PMID 25897172

[Mus musculus] Alveolar macrophages detect respiratory syncytial virus (RSV) via the Mavs /Ddx58 pathway and are a major source of type I interferons upon RSV infection.

PMID 26633895

[Mus musculus] Transgenic picornavirus RNA-dependent RNA polymerase (RdRP) expression in mice produces a quantitatively dramatic, sustained, effective antiviral interferon-stimulated genes (ISG) network, which requires the MDA5-MAVS pathway.

PMID 26246171

[Mus musculus] March5 modulates Mavs-mediated antiviral signalling, preventing excessive immune reactions.

PMID 26348439

[Mus musculus] Baiap2l1 recruits Ube2i to sumoylate Pcbp2, which causes its cytoplasmic translocation during viral infection and the sumoylated Pcbp2 associates with Mavs to initiate its degradation, leading to downregulation of antiviral responses.

Entrez Gene

Summary

This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000088888:
This gene encodes an intermediary protein necessary in the virus-triggered beta interferon signaling pathways. It is required for activation of transcription factors which regulate expression of beta interferon and contributes to antiviral immunity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

Gene Information

Type

Protein coding

Genomic Location

Chromosome 13:51797279-51809475

Strand

Reverse strand

Band

Transcripts

ENSBTAT00000018013

ENSBTAP00000018013

Interactions

Number of Interactions

This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 90 interaction(s) predicted by orthology.

Predicted by orthology
Total	90 [view]

Gene Ontology

Molecular Function

Accession	GO Term
GO:0004871	signal transducer activity
GO:0005515	protein binding
GO:0019901	protein kinase binding
GO:0050700	CARD domain binding

Biological Process

GO:0001934	positive regulation of protein phosphorylation
GO:0002218	activation of innate immune response
GO:0002230	positive regulation of defense response to virus by host
GO:0007165	signal transduction
GO:0032481	positive regulation of type I interferon production
GO:0032727	positive regulation of interferon-alpha production
GO:0032728	positive regulation of interferon-beta production
GO:0032757	positive regulation of interleukin-8 production
GO:0032760	positive regulation of tumor necrosis factor production
GO:0033160	positive regulation of protein import into nucleus, translocation
GO:0039529	RIG-I signaling pathway
GO:0042742	defense response to bacterium
GO:0042993	positive regulation of transcription factor import into nucleus
GO:0043123	positive regulation of I-kappaB kinase/NF-kappaB signaling
GO:0045071	negative regulation of viral genome replication
GO:0045087	innate immune response
GO:0045944	positive regulation of transcription from RNA polymerase II promoter
GO:0051091	positive regulation of sequence-specific DNA binding transcription factor activity
GO:0051607	defense response to virus
GO:0060340	positive regulation of type I interferon-mediated signaling pathway
GO:0071360	cellular response to exogenous dsRNA
GO:0071651	positive regulation of chemokine (C-C motif) ligand 5 production
GO:0071660	positive regulation of IP-10 production
GO:1900063	regulation of peroxisome organization