Pepino mosaic virus antagonizes plant m6A modification by promoting the autophagic degradation of the m6A writer HAKAI

IF 4.6 4区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY aBIOTECH Pub Date : 2023-02-23 DOI:10.1007/s42994-023-00097-6
Hao He, Linhao Ge, Zhaolei Li, Xueping Zhou, Fangfang Li
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引用次数: 3

Abstract

Autophagy plays an active anti-viral role in plants. Increasing evidence suggests that viruses can inhibit or manipulate autophagy, thereby winning the arms race between plants and viruses. Here, we demonstrate that overexpression of an m6A writer from Solanum lycopersicum, SlHAKAI, could negatively regulate pepino mosaic virus (PepMV) infection, inhibit viral RNA and protein accumulations by affecting viral m6A levels in tomato plants and vice versa. The PepMV-encoded RNA-dependent RNA polymerase (RdRP) directly interacts with SlHAKAI and reduces its protein accumulation. The RdRP-mediated decreased protein accumulation of SlHAKAI is sensitive to the autophagy inhibitor 3-methyladenine and is compromised by knocking down a core autophagy gene. Furthermore, PepMV RdRP could interact with an essential autophagy-related protein, SlBeclin1. RdRP, SlHAKAI, and SlBeclin1 interaction complexes form bright granules in the cytoplasm. Silencing of Beclin1 in Nicotiana benthamiana plants abolishes the RdRP-mediated degradation of SlHAKAI, indicating the requirement of Beclin1 in this process. This study uncovers that the PepMV RdRP exploits the autophagy pathway by interacting with SlBeclin1 to promote the autophagic degradation of the SlHAKAI protein, thereby inhibiting the m6A modification-mediated plant defense responses.

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Pepino花叶病毒通过促进m6A作者HAKAI的自噬降解来拮抗植物m6A修饰
自噬在植物中起着积极的抗病毒作用。越来越多的证据表明,病毒可以抑制或操纵自噬,从而赢得植物和病毒之间的军备竞赛。在这里,我们证明了来自番茄的m6A作家SlHAKAI的过表达可以负调控pepino mosaic virus(PepMV)感染,通过影响番茄植株中的病毒m6A水平来抑制病毒RNA和蛋白质积累,反之亦然。PepMV编码的RNA依赖性RNA聚合酶(RdRP)直接与SlHAKAI相互作用并减少其蛋白质积累。RdRP介导的SlHAKAI蛋白质积累减少对自噬抑制剂3-甲基腺嘌呤敏感,并通过敲低核心自噬基因而受损。此外,PepMV-RdRP可以与一种重要的自噬相关蛋白SlBeclin1相互作用。RdRP、SlHAKAI和SlBeclin1相互作用复合物在细胞质中形成明亮的颗粒。本氏烟草中Beclin1的沉默消除了RdRP介导的SlHAKAI的降解,表明该过程中需要Beclin1。本研究发现,PepMV RdRP通过与SlBeclin1相互作用来利用自噬途径,促进SlHAKAI蛋白的自噬降解,从而抑制m6A修饰介导的植物防御反应。
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CiteScore
7.70
自引率
2.80%
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0
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