钙传感器AtCML8通过调节油菜素内酯信号通路参与拟南芥植物细胞生长。

IF 5.7 1区 生物学 Q1 PLANT SCIENCES The Plant Journal Pub Date : 2024-12-02 DOI:10.1111/tpj.17179
Amandine Lucchin, Hélène Fouassier, Eugénie Robe, Malick Mbengue, Marielle Aguilar, Hélène San Clemente, Grégory Vert, Jean-Philippe Galaud, Didier Aldon
{"title":"钙传感器AtCML8通过调节油菜素内酯信号通路参与拟南芥植物细胞生长。","authors":"Amandine Lucchin,&nbsp;Hélène Fouassier,&nbsp;Eugénie Robe,&nbsp;Malick Mbengue,&nbsp;Marielle Aguilar,&nbsp;Hélène San Clemente,&nbsp;Grégory Vert,&nbsp;Jean-Philippe Galaud,&nbsp;Didier Aldon","doi":"10.1111/tpj.17179","DOIUrl":null,"url":null,"abstract":"<p>Calcium signaling plays an essential role in integrating plant responses to diverse stimuli and regulating growth and development. While some signaling components and their roles are well-established, such as the ubiquitous calmodulin (CaM) sensor, plants possess a broader repertoire of calcium sensors. Notably, CaM-like proteins (CMLs) represent a poorly characterized class for which interacting partners and biological functions remain largely elusive. Our work investigates the role of <i>Arabidopsis thaliana</i> CML8 that exhibits a unique expression profile in seedlings. A reverse genetic approach revealed a function of CML8 in regulating root growth and hypocotyl elongation. RNA-seq analyses highlighted CML8 association with the regulation of numerous genes involved in growth and brassinosteroid (BR) signaling. Using co-immunoprecipitation experiments, we demonstrated that CML8 interacts with the BR receptor, BRI1, <i>in planta</i> in a ligand-dependent manner. This finding suggests the existence of a novel regulatory step in the BR pathway, involving calcium signaling.</p>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"121 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11712026/pdf/","citationCount":"0","resultStr":"{\"title\":\"The calcium sensor AtCML8 contributes to Arabidopsis plant cell growth by modulating the brassinosteroid signaling pathway\",\"authors\":\"Amandine Lucchin,&nbsp;Hélène Fouassier,&nbsp;Eugénie Robe,&nbsp;Malick Mbengue,&nbsp;Marielle Aguilar,&nbsp;Hélène San Clemente,&nbsp;Grégory Vert,&nbsp;Jean-Philippe Galaud,&nbsp;Didier Aldon\",\"doi\":\"10.1111/tpj.17179\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Calcium signaling plays an essential role in integrating plant responses to diverse stimuli and regulating growth and development. While some signaling components and their roles are well-established, such as the ubiquitous calmodulin (CaM) sensor, plants possess a broader repertoire of calcium sensors. Notably, CaM-like proteins (CMLs) represent a poorly characterized class for which interacting partners and biological functions remain largely elusive. Our work investigates the role of <i>Arabidopsis thaliana</i> CML8 that exhibits a unique expression profile in seedlings. A reverse genetic approach revealed a function of CML8 in regulating root growth and hypocotyl elongation. RNA-seq analyses highlighted CML8 association with the regulation of numerous genes involved in growth and brassinosteroid (BR) signaling. Using co-immunoprecipitation experiments, we demonstrated that CML8 interacts with the BR receptor, BRI1, <i>in planta</i> in a ligand-dependent manner. This finding suggests the existence of a novel regulatory step in the BR pathway, involving calcium signaling.</p>\",\"PeriodicalId\":233,\"journal\":{\"name\":\"The Plant Journal\",\"volume\":\"121 1\",\"pages\":\"\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2024-12-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11712026/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Plant Journal\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/tpj.17179\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.17179","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

摘要

钙信号在整合植物对各种刺激的反应和调节植物生长发育中起着重要作用。虽然一些信号成分及其作用已经确定,如无处不在的钙调素(CaM)传感器,但植物拥有更广泛的钙传感器。值得注意的是,cam样蛋白(cml)是一类特征不明确的蛋白,其相互作用伙伴和生物学功能在很大程度上仍然难以捉摸。我们的工作研究了拟南芥CML8在幼苗中独特表达谱的作用。反向遗传方法揭示了CML8在调节根生长和下胚轴伸长方面的功能。RNA-seq分析强调CML8与许多参与生长和油菜素内酯(BR)信号传导的基因调控相关。通过共免疫沉淀实验,我们证明了CML8与植物BR受体BRI1以配体依赖的方式相互作用。这一发现表明在BR通路中存在一个新的调控步骤,涉及钙信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The calcium sensor AtCML8 contributes to Arabidopsis plant cell growth by modulating the brassinosteroid signaling pathway

Calcium signaling plays an essential role in integrating plant responses to diverse stimuli and regulating growth and development. While some signaling components and their roles are well-established, such as the ubiquitous calmodulin (CaM) sensor, plants possess a broader repertoire of calcium sensors. Notably, CaM-like proteins (CMLs) represent a poorly characterized class for which interacting partners and biological functions remain largely elusive. Our work investigates the role of Arabidopsis thaliana CML8 that exhibits a unique expression profile in seedlings. A reverse genetic approach revealed a function of CML8 in regulating root growth and hypocotyl elongation. RNA-seq analyses highlighted CML8 association with the regulation of numerous genes involved in growth and brassinosteroid (BR) signaling. Using co-immunoprecipitation experiments, we demonstrated that CML8 interacts with the BR receptor, BRI1, in planta in a ligand-dependent manner. This finding suggests the existence of a novel regulatory step in the BR pathway, involving calcium signaling.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
期刊最新文献
Advances and opportunities for computational interrogation of plant proteins. Phylogenetic constraints, conservatism, and convergence shape three-dimensional variation in flower morphology of a tropical orchid radiation. PHR1 mediates rapid high light responses and acclimation to high photosynthetic activity. The MYB41-MYB74 module and VOZ1 transcription factor synergistically regulate aliphatic suberin monomer biosynthesis in Chenopodium quinoa. Integrative network-level rewiring of photosynthetic metabolism boosts phycocyanin biosynthesis in cyanobacterial chassis.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1