ATG10S promotes IFNL1 expression and autophagic degradation of multiple viral proteins mediated by IFNL1.

Autophagy Pub Date : 2024-10-01 Epub Date: 2024-06-11 DOI:10.1080/15548627.2024.2361580
Miao-Qing Zhang, Jian-Rui Li, Lu Yang, Zong-Gen Peng, Shuo Wu, Jing-Pu Zhang
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Abstract

ATG10S is a newly discovered subtype of the autophagy protein ATG10. It promotes complete macroautophagy/autophagy, degrades multiple viral proteins, and increases the expression of type III interferons. Here, we aimed to investigate the mechanism of ATG10S cooperation with IFNL1 to degrade viral proteins from different viruses. Using western blot, immunoprecipitation (IP), tandem sensor RFP-GFP-LC3B and in situ proximity ligation assays, we showed that exogenous recombinant ATG10S protein (rHsATG10S) could enter into cells through clathrin, and ATG10S combined with ATG7 with IFNL1 assistance to facilitate ATG12-ATG5 conjugation, thereby contributing to the autophagosome formation in multiple cell lines containing different virions or viral proteins. The results of DNA IP and luciferase assays also showed that ATG10S was able to directly bind to a core motif (CAAGGG) within a binding site of transcription factor ZNF460 on the IFNL1 promoter, by which IFNL1 transcription was activated. These results clarified that ATG10S promoted autophagosome formation with the assistance of IFNL1 to ensure autophagy flux and autophagic degradation of multiple viral proteins and that ATG10S could also act as a novel transcription factor to promote IFNL1 gene expression. Importantly, this study further explored the antiviral mechanism of ATG10S interaction with type III interferon and provided a theoretical basis for the development of ATG10S into a new broad-spectrum antiviral protein drug.Abbreviation: ATG: autophagy related; ATG10S: the shorter isoform of autophagy-related 10; CC50: half cytotoxicity concentration; CCV: clathrin-coated transport vesicle; CLTC: clathrin heavy chain; CM: core motif; co-IP: co-immunoprecipitation; CPZ: chlorpromazine; ER: endoplasmic reticulum; HCV: hepatitis C virus; HBV: hepatitis B virus; HsCoV-OC43: Human coronavirus OC43; IFN: interferon; PLA: proximity ligation assay; rHsATG10S: recombinant human ATG10S protein; RLU: relative light unit; SQSTM1: sequestosome 1; ZNF: zinc finger protein.

ATG10S 可促进 IFNL1 的表达和 IFNL1 介导的多种病毒蛋白的自噬降解。
ATG10S 是新发现的自噬蛋白 ATG10 的一种亚型。它能促进完全大自噬/自噬,降解多种病毒蛋白,并增加Ⅲ型干扰素的表达。在此,我们旨在研究 ATG10S 与 IFNL1 合作降解不同病毒的病毒蛋白的机制。通过Western印迹、免疫沉淀(IP)、串联传感器RFP-GFP-LC3B和原位近接实验,我们发现外源重组ATG10S蛋白(rHsATG10S)可通过凝集素进入细胞,ATG10S在IFNL1的协助下与ATG7结合,促进ATG12-ATG5共轭,从而在含有不同病毒或病毒蛋白的多个细胞系中促进自噬体的形成。DNA IP 和荧光素酶检测的结果还表明,ATG10S 能够直接与 IFNL1 启动子上转录因子 ZNF460 结合位点内的核心基序(CAAGGG)结合,从而激活 IFNL1 的转录。这些结果明确了ATG10S在IFNL1的协助下促进自噬体的形成,以确保自噬通量和多种病毒蛋白的自噬降解,而且ATG10S还可以作为一种新型转录因子促进IFNL1基因的表达。重要的是,该研究进一步探索了ATG10S与III型干扰素相互作用的抗病毒机制,为将ATG10S开发成新型广谱抗病毒蛋白药物提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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