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

Author:

Lee Keun Pyo1ORCID,Liu Kaiwei12ORCID,Kim Eun Yu3ORCID,Medina-Puche Laura1ORCID,Dong Haihong1ORCID,Di Minghui12ORCID,Singh Rahul Mohan1ORCID,Li Mengping1ORCID,Qi Shan12ORCID,Meng Zhuoling12ORCID,Cho Jungnam34ORCID,Zhang Heng1ORCID,Lozano-Duran Rosa1ORCID,Kim Chanhong1ORCID

Affiliation:

1. Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences (CEMPS), Chinese Academy of Sciences , Shanghai 200032 , China

2. University of the Chinese Academy of Sciences , Beijing 100049 , China

3. National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences (CEMPS), Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences , Shanghai 200032 , China

4. CAS-JIC Centre of Excellence for Plant and Microbial Science, Chinese Academy of Sciences , Shanghai 200032 , China

Abstract

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.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

Reference72 articles.

1. Quantifying mRNA targeting to P-bodies in living human cells reveals their dual role in mRNA decay and storage;Aizer;J Cell Sci,2014

2. RNA granules: post-transcriptional and epigenetic modulators of gene expression;Anderson;Nat Rev Mol Cell Biol,2009

3. An m(6)A-YTH module controls developmental timing and morphogenesis in Arabidopsis;Arribas-Hernandez;Plant Cell,2018

4. Principles of mRNA targeting via the Arabidopsis m(6)A-binding protein ECT2;Arribas-Hernandez;eLife,2021

5. The YTHDF proteins ECT2 and ECT3 bind largely overlapping target sets and influence target mRNA abundance, not alternative polyadenylation;Arribas-Hernandez;eLife,2021

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3