{"title":"HyperTRIBE mapping of the RNA m6A demethylase ALKBH9 binding sites in bamboo reveals its role in plant defense","authors":"Huihui Wang, Huiyuan Wang, Yue Jia, Tuhe Li, Siyu Yang, Yandong Jin, Zaofa Zhong, Wenting Bai, Huakun Zheng, Liangzhen Zhao, Chentao Lin, Anireddy S N Reddy, Hangxiao Zhang, Lianfeng Gu","doi":"10.1093/plphys/kiaf457","DOIUrl":null,"url":null,"abstract":"RNA demethylation plays an important role in diverse biological processes. Intriguingly, RNA demethylation has not been reported in bamboo, which is known for its rapid growth. PheALKBH9, an m6A demethylase in bamboo, was stably transformed into rice and increased its susceptibility to rice blast disease. Heterologous expression of PheALKBH9 reduced the overall m6A modification levels in rice. Using HyperTRIBE (Targets of RNA-binding proteins Identified By Editing), we identified evolutionarily conserved PheALKBH9 target RNAs in both rice and Moso bamboo. Overexpression of PheALKBH9 led to higher protein expression and shorter poly(A) tails. Notably, PheALKBH9 directly bound to CCR4-associated factor1 (CAF1G) and Poly(A)-binding genes (PABPC1 and PABPC2), potentially modulating poly(A) tail lengths. In addition, PheALKBH9 also bound to and removed m6A modifications from Perox4, JAZ7 and METS2, key players in plant immunity, suggesting that PheALKBH9 plays a role in plant disease resistance. In summary, our study unveils a previously unknown role of PheALKBH9-mediated m6A demethylation in response to blast disease and provides insights into its mechanisms in monocotyledonous plants.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"39 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf457","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
RNA demethylation plays an important role in diverse biological processes. Intriguingly, RNA demethylation has not been reported in bamboo, which is known for its rapid growth. PheALKBH9, an m6A demethylase in bamboo, was stably transformed into rice and increased its susceptibility to rice blast disease. Heterologous expression of PheALKBH9 reduced the overall m6A modification levels in rice. Using HyperTRIBE (Targets of RNA-binding proteins Identified By Editing), we identified evolutionarily conserved PheALKBH9 target RNAs in both rice and Moso bamboo. Overexpression of PheALKBH9 led to higher protein expression and shorter poly(A) tails. Notably, PheALKBH9 directly bound to CCR4-associated factor1 (CAF1G) and Poly(A)-binding genes (PABPC1 and PABPC2), potentially modulating poly(A) tail lengths. In addition, PheALKBH9 also bound to and removed m6A modifications from Perox4, JAZ7 and METS2, key players in plant immunity, suggesting that PheALKBH9 plays a role in plant disease resistance. In summary, our study unveils a previously unknown role of PheALKBH9-mediated m6A demethylation in response to blast disease and provides insights into its mechanisms in monocotyledonous plants.
RNA去甲基化在多种生物过程中起着重要作用。有趣的是,以快速生长而闻名的竹子中没有RNA去甲基化的报道。竹子中的m6A去甲基化酶PheALKBH9稳定转化到水稻中,增加了水稻对稻瘟病的易感性。PheALKBH9的异源表达降低了水稻中m6A的总体修饰水平。利用HyperTRIBE (target of RNA-binding proteins Identified By Editing)技术,我们在水稻和毛竹中发现了进化上保守的PheALKBH9靶rna。PheALKBH9过表达导致蛋白表达增加,聚(A)尾变短。值得注意的是,PheALKBH9直接结合ccr4相关因子1 (CAF1G)和Poly(A)结合基因(PABPC1和PABPC2),可能调节Poly(A)尾巴长度。此外,PheALKBH9还结合并去除植物免疫的关键基因Perox4、JAZ7和METS2的m6A修饰,表明PheALKBH9在植物抗病中发挥作用。总之,我们的研究揭示了phealkbh9介导的m6A去甲基化在对blast疾病的反应中以前未知的作用,并为其在单子叶植物中的机制提供了见解。
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.