The m6A reader ECT1 drives mRNA sequestration to dampen salicylic acid–dependent stress responses in Arabidopsis

Keun Pyo Lee, Kaiwei Liu, Eun Yu Kim, Laura Medina-Puche, Haihong Dong, Minghui Di, Rahul Mohan Singh, Mengping Li, Shan Qi, Zhuoling Meng, Jungnam Cho, Heng Zhang, Rosa Lozano-Duran, Chanhong Kim
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Abstract

N 6-methyladenosine (m6A) is a common epitranscriptional mRNA modification in eukaryotes. Thirteen putative m6A readers, mostly annotated as EVOLUTIONARILY CONSERVED C-TERMINAL REGION (ECT) proteins, have been identified in Arabidopsis (Arabidopsis thaliana), but few have been characterized. Here, we show that the Arabidopsis m6A reader ECT1 modulates salicylic acid (SA)-mediated plant stress responses. ECT1 undergoes liquid-liquid phase separation in vitro, and its N-terminal prion-like domain is critical for forming in vivo cytosolic biomolecular condensates in response to SA or bacterial pathogens. Fluorescence-activated particle sorting coupled with quantitative PCR analyses unveiled that ECT1 sequesters SA-induced m6A modification-prone mRNAs through its conserved aromatic cage to facilitate their decay in cytosolic condensates, thereby dampening SA-mediated stress responses. Consistent with this finding, ECT1 overexpression promotes bacterial multiplication in plants. Collectively, our findings unequivocally link ECT1-associated cytosolic condensates to SA-dependent plant stress responses, advancing the current understanding of m6A readers and the SA signaling network.
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m6A读取器ECT1驱动mRNA封存以抑制拟南芥中水杨酸依赖的应激反应
n6 -甲基腺苷(m6A)是真核生物中常见的mRNA表转录修饰。在拟南芥(Arabidopsis thaliana)中已经鉴定出13个假定的m6A读取器,其中大多数被注释为进化保守的c -末端区(ECT)蛋白,但很少被鉴定。在这里,我们发现拟南芥m6A读取器ECT1调节水杨酸(SA)介导的植物胁迫反应。ECT1在体外经历液-液相分离,其n端朊蛋白样结构域对于在体内响应SA或细菌病原体形成胞质生物分子凝聚体至关重要。荧光激活颗粒分选结合定量PCR分析表明,ECT1通过其保守的芳香笼隔离sa诱导的m6A修饰易感mrna,促进其在细胞质凝聚物中的衰变,从而抑制sa介导的应激反应。与这一发现一致,ECT1过表达促进了植物中的细菌增殖。总的来说,我们的研究结果明确地将ect1相关的细胞质凝聚物与SA依赖的植物胁迫反应联系起来,推进了目前对m6A读取器和SA信号网络的理解。
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