Deficiency of Arabidopsis SMO2 triggers an ANAC082-Dependent pathway to regulate root apical meristem

IF 4.8 3区 生物学 Q1 PLANT SCIENCES
Journal of plant physiology Pub Date : 2026-01-01 Epub Date: 2025-11-19 DOI:10.1016/j.jplph.2025.154651
Aiming Xing , Xiaoyu Wang , Jing Gao , Cheng Zeng , Ning Li , Chunfei Wang , Xiaoqing Wang , Zhenguo Shen , Zhubing Hu
{"title":"Deficiency of Arabidopsis SMO2 triggers an ANAC082-Dependent pathway to regulate root apical meristem","authors":"Aiming Xing ,&nbsp;Xiaoyu Wang ,&nbsp;Jing Gao ,&nbsp;Cheng Zeng ,&nbsp;Ning Li ,&nbsp;Chunfei Wang ,&nbsp;Xiaoqing Wang ,&nbsp;Zhenguo Shen ,&nbsp;Zhubing Hu","doi":"10.1016/j.jplph.2025.154651","DOIUrl":null,"url":null,"abstract":"<div><div>Root apical meristem (RAM) maintains sustained root development, which is intricately coordinated by a series of biological processes integrating internal and external cues. Here, we present evidence that SMALL ORGAN 2 (SMO2) is required for the maintenance of RAM. Deficiency of SMO2 resulted in disorganization of the stem cell niche (SCN) and the presence of dead cells in RAM, independent of DNA damage. Moreover, following chemically induced wounding, excision of root tips, or removal of whole roots, the regeneration capacity of <em>smo2</em> mutants was dramatically lower than that of wild-type plants. Mechanistically, SMO2 is necessary for 18S rRNA methylation at position G1581, which may be associated with abnormal ribosome profiles in <em>smo2</em> mutants. Further analysis showed that deficiency of SMO2 markedly reduced the translation efficiency of genes involved in polar auxin transport, thereby reducing auxin accumulation in the RAM. Surprisingly, an additional deletion of ANAC082, which encodes a known transcriptional mediator of ribosomal stress-induced developmental adaptations, effectively restored the disordered SCN and cell death phenotypes in <em>smo2</em> mutants. Collectively, our findings demonstrate that SMO2-mediated translational regulation plays an important role in auxin accumulation in root tips. This process appears to be essential for sustaining RAM activity, as indicated by the structural disorganization of root tips in <em>smo2</em> mutants. Notably, this phenotypic manifestation is mechanistically dependent on ANAC082.</div></div>","PeriodicalId":16808,"journal":{"name":"Journal of plant physiology","volume":"316 ","pages":"Article 154651"},"PeriodicalIF":4.8000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of plant physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0176161725002330","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Root apical meristem (RAM) maintains sustained root development, which is intricately coordinated by a series of biological processes integrating internal and external cues. Here, we present evidence that SMALL ORGAN 2 (SMO2) is required for the maintenance of RAM. Deficiency of SMO2 resulted in disorganization of the stem cell niche (SCN) and the presence of dead cells in RAM, independent of DNA damage. Moreover, following chemically induced wounding, excision of root tips, or removal of whole roots, the regeneration capacity of smo2 mutants was dramatically lower than that of wild-type plants. Mechanistically, SMO2 is necessary for 18S rRNA methylation at position G1581, which may be associated with abnormal ribosome profiles in smo2 mutants. Further analysis showed that deficiency of SMO2 markedly reduced the translation efficiency of genes involved in polar auxin transport, thereby reducing auxin accumulation in the RAM. Surprisingly, an additional deletion of ANAC082, which encodes a known transcriptional mediator of ribosomal stress-induced developmental adaptations, effectively restored the disordered SCN and cell death phenotypes in smo2 mutants. Collectively, our findings demonstrate that SMO2-mediated translational regulation plays an important role in auxin accumulation in root tips. This process appears to be essential for sustaining RAM activity, as indicated by the structural disorganization of root tips in smo2 mutants. Notably, this phenotypic manifestation is mechanistically dependent on ANAC082.
拟南芥SMO2缺失触发anac082依赖通路调控根尖分生组织
根尖分生组织(Root apical merisystem, RAM)维持着根系的持续发育,这一过程是由一系列复杂的生物过程协调而成的。在这里,我们提出的证据表明,小器官2 (SMO2)是维持RAM所必需的。SMO2的缺乏导致RAM中干细胞生态位(SCN)的破坏和死细胞的存在,而这与DNA损伤无关。此外,在化学诱导损伤、根尖切除或全根切除后,smo2突变体的再生能力显著低于野生型植株。从机制上讲,SMO2是G1581位点18S rRNA甲基化的必要条件,这可能与SMO2突变体中异常的核糖体谱有关。进一步分析表明,缺乏SMO2显著降低了参与生长素极性转运的基因的翻译效率,从而减少了生长素在RAM中的积累。令人惊讶的是,ANAC082的额外缺失,编码核糖体应激诱导的发育适应的已知转录介质,有效地恢复了smo2突变体中紊乱的SCN和细胞死亡表型。总之,我们的研究结果表明,smo2介导的翻译调控在根尖生长素积累中起着重要作用。这一过程似乎是维持RAM活性所必需的,正如smo2突变体根尖结构紊乱所表明的那样。值得注意的是,这种表型表现在机制上依赖于ANAC082。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of plant physiology
Journal of plant physiology 生物-植物科学
CiteScore
7.20
自引率
4.70%
发文量
196
审稿时长
32 days
期刊介绍: The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication. The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书