TBK1和IKBKE/IKKi对选择性自噬受体TAX1BP1的磷酸化促进了Atg8家族蛋白对MAVS聚集体的依赖性清除。

Jesse White, Young Bong Choi, Jiawen Zhang, Mai Tram Vo, Chaoxia He, Kashif Shaikh, Edward W Harhaj
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引用次数: 0

摘要

TAX1BP1 是一种选择性大自噬/自噬受体,可抑制 NFKB 和类 RIGI 受体(RLR)信号传导,从而防止过度炎症并维持体内平衡。选择性自噬受体(如 SQSTM1/p62 和 OPTN)会被激酶 TBK1 磷酸化,从而激发其选择性自噬功能。然而,TAX1BP1 在基础条件下或在 RNA 病毒感染期间是否受 TBK1 或其他激酶的调控尚不清楚。在这里,我们发现 TBK1 和 IKBKE/IKKi 具有冗余功能,可使 TAX1BP1 磷酸化,并通过典型的大自噬调节其自噬周转。TAX1BP1 磷酸化促进其定位到溶酶体,从而导致其降解。此外,我们还发现,在水泡性口炎病毒感染期间,TAX1BP1 以一种不依赖 Atg8 家族蛋白的方式靶向溶酶体。此外,TAX1BP1 在清除 MAVS 聚集物中发挥着关键作用,而 TAX1BP1 的磷酸化控制着它的 MAVS aggrephagy 功能。总之,我们的数据支持这样一个模型,即 TBK1 和 IKBKE 许可 TAX1BP1 选择性自噬功能来抑制 MAVS 和 RLR 信号转导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphorylation of the selective autophagy receptor TAX1BP1 by TBK1 and IKBKE/IKKi promotes ATG8-family protein-dependent clearance of MAVS aggregates.

TAX1BP1 is a selective macroautophagy/autophagy receptor that inhibits NFKB and RIGI-like receptor (RLR) signaling to prevent excessive inflammation and maintain homeostasis. Selective autophagy receptors such as SQSTM1/p62 and OPTN are phosphorylated by the kinase TBK1 to stimulate their selective autophagy function. However, it is unknown if TAX1BP1 is regulated by TBK1 or other kinases under basal conditions or during RNA virus infection. Here, we found that TBK1 and IKBKE/IKKi function redundantly to phosphorylate TAX1BP1 and regulate its autophagic turnover through canonical macroautophagy. TAX1BP1 phosphorylation promotes its localization to lysosomes, resulting in its degradation. Additionally, we found that during vesicular stomatitis virus infection, TAX1BP1 is targeted to lysosomes in an ATG8-family protein-independent manner. Furthermore, TAX1BP1 plays a critical role in the clearance of MAVS aggregates, and phosphorylation of TAX1BP1 controls its MAVS aggrephagy function. Together, our data support a model whereby TBK1 and IKBKE license TAX1BP1-selective autophagy function to inhibit MAVS and RLR signaling.Abbreviations: ATG: autophagy related; BafA1: bafilomycin A1; CALCOCO2: calcium binding and coiled-coil domain 2; GFP: green fluorescent protein; IFA: indirect immunofluorescence assay; IFN: interferon; IκB: inhibitor of nuclear factor kappa B; IKK: IκB kinase; IRF: interferon regulatory factor; KO: knockout; LAMP1: lysosomal associated membrane protein 1; LIR: LC3-interacting region; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MAVS: mitochondrial antiviral signaling protein; MEF: mouse embryonic fibroblast; MOI: multiplicity of infection; IKBKG/NEMO: inhibitor of nuclear factor kappa B kinase regulatory subunit gamma; NFKB: nuclear factor kappa B; OPTN: optineurin; Poly(I:C): polyinosinic-polycytidylic acid; RB1CC1/FIP200: RB1 inducible coiled-coil 1; RIGI: RNA sensor RIG-I; RLR: RIGI-like receptor; SDD-AGE: semi-denaturing detergent-agarose gel electrophoresis; SeV: Sendai virus; SLR: SQSTM1-like receptor; SQSTM1: sequestosome 1; TAX1BP1: Tax1 binding protein 1; TBK1: TANK binding kinase 1; TNF: tumor necrosis factor; TRAF: TNF receptor associated factor; VSV: vesicular stomatitis virus; ZnF: zinc finger.

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