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Regulation of MDA5-MAVS Antiviral Signaling Axis by TRIM25 through TRAF6-Mediated NF-κB Activation

机译:TRIM25通过TRAF6介导的NF-κB激活调节MDA5-MAVS抗病毒信号轴

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摘要

Tripartite motif protein 25 (TRIM25), mediates K63-linked polyubiquitination of Retinoic acid inducible gene I (RIG-I) that is crucial for downstream antiviral interferon signaling. Here, we demonstrate that TRIM25 is required for melanoma differentiation-associated gene 5 (MDA5) and MAVS mediated activation of NF-κB and interferon production. TRIM25 is required for the full activation of NF-κB at the downstream of MAVS, while it is not involved in IRF3 nuclear translocation. Mechanical studies showed that TRIM25 is involved in TRAF6-mediated NF-κB activation. These collectively indicate that TRIM25 plays an additional role in RIG-I/MDA5 signaling other than RIG-I ubiquitination via activation of NF-κB.
机译:三方基序蛋白25(TRIM25)介导视黄酸诱导型基因I(RIG-I)的K63连锁多聚泛素化,这对于下游抗病毒干扰素信号传导至关重要。在这里,我们证明TRIM25是黑色素瘤分化相关基因5(MDA5)和MAVS介导的NF-κB激活和干扰素产生所必需的。 TRIM25是在MAVS下游完全激活NF-κB所必需的,而它不参与IRF3核易位。力学研究表明TRIM25参与TRAF6介导的NF-κB活化。这些共同表明,TRIM25在RIG-I / MDA5信号传导中除了通过激活NF-κB的RIG-I泛素化外,还扮演着其他角色。

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