A conserved lysine/arginine-rich motif is essential for the autophagic degradation of potyviral 6K1 protein and virus infection

文献类型： 外文期刊

第一作者： Hu, Weiyao

作者： Hu, Weiyao;Deng, Changhui;Qin, Li;Liu, Peilan;Wang, Linxi;Wang, Xaioqing;Shi, Wei;Aziz, Asma;Dai, Zhaoji;Cui, Hongguang;Hu, Weiyao;Deng, Changhui;Qin, Li;Liu, Peilan;Wang, Linxi;Wang, Xaioqing;Shi, Wei;Aziz, Asma;Dai, Zhaoji;Cui, Hongguang;Li, Fangfang;Cheng, Xiaofei;Wang, Aiming;Xiang, Xiaohua

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关键词： Potyvirus; autophagy; protein degradation; point mutation; pro-viral role

期刊名称：JOURNAL OF VIROLOGY （ 影响因子：3.8； 五年影响因子：3.9 ）

ISSN： 0022-538X

年卷期： 2025 年 99 卷 3 期

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收录情况： SCI

摘要： Potyviruses possess one positive-sense single-stranded RNA genome, mainly dependent on polyprotein processing as the expression strategy. The resulting polyproteins are proteolytically processed by three virus-encoded proteases into 11 or 12 mature proteins. One such factor, 6 kDa peptide 1 (6K1), is an understudied viral factor. Its function in viral infection remains largely mysterious. This study is to reveal part of its roles by using pepper veinal mottle virus (PVMV) as the model. Alanine substitution screening analysis revealed that 15 of 17 conserved residues across potyviral 6K1 sequences are essential for PVMV infection. However, 6K1 protein is less accumulated in virus-infected cells, although P3-6K1 and 6K1-CI junctions are efficiently processed by NIa-Pro for its release, indicating that 6K1 undergoes a self-degradation event. Mutating the cleavage site to prevent NIa-Pro processing abolishes viral infection, suggesting that the generation of 6K1 along with its degradation might be important for viral multiplication. We corroborated that cellular autophagy is engaged in 6K1's degradation. Individual engineering of the 15 6K1 variants into PVMV allows their expression along with viral infection. Five of such variants, D30A, V32A, K34A, L36A, and L39A, significantly interfere with viral infection. The five residues are enclosed in a conserved lysine/arginine-rich motif; four of them appear crucial in engaging autophagy-mediated self-degradation. Based on these data, we envisaged a scenario which potyviral 6K1s interact with an unknown anti-viral component to be co-degraded by autophagy to promote viral infection.

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