Xuan Zhou, Binghou Li, Jiahuizi Li, Yufei Sun, Ruohan Xie, Tetsuya Higashiyama, Shi Xiao, Guorong Xin, Shihao Su
{"title":"机械敏感离子通道通过操纵托伦尼亚的钙特征来控制触摸触发的柱头运动","authors":"Xuan Zhou, Binghou Li, Jiahuizi Li, Yufei Sun, Ruohan Xie, Tetsuya Higashiyama, Shi Xiao, Guorong Xin, Shihao Su","doi":"10.1038/s41467-025-61770-6","DOIUrl":null,"url":null,"abstract":"<p>Rapid movements of plant structures triggered by mechanical force have been documented for centuries; however, how plant cells sense mechanical stimuli and generate rapid response remains unknown. Here we show the central role of a mechanosensitive channel gene in touch-triggered rapid stigma movement of <i>Torenia fournieri</i>. <i>T. fournieri</i> possesses a bilobed stigma sensitive to mechanical stimuli. Using live-cell calcium imaging, we detect that touch induces a wave of cytosolic calcium ([Ca<sup>2+</sup>]<sub>cyt</sub>) essential for stigma movement. Transcriptomic analysis reveals distinct gene expression profiles between the stigma and style, leading to the identification of the <i>MscS-like</i> gene <i>JUE1</i>, predominantly expressed in stigmas. Stigmas of <i>jue1</i> mutants exhibit complete loss of touch-triggered movement, confirming its role as a key regulator in sensitive stigma movement. JUE1 is required for rapid propagation of the touch-induced [Ca<sup>2+</sup>]<sub>cyt</sub>, as cell-to-cell spreading of the [Ca<sup>2+</sup>]<sub>cyt</sub> wave is impaired in the <i>jue1</i>. To conclude, we report a plant mechanosensitive ion channel involved in touch-triggered organ movement by modulating calcium dynamics.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"32 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A mechanosensitive ion channel controls touch-triggered stigma movement through manipulation of calcium signature in Torenia\",\"authors\":\"Xuan Zhou, Binghou Li, Jiahuizi Li, Yufei Sun, Ruohan Xie, Tetsuya Higashiyama, Shi Xiao, Guorong Xin, Shihao Su\",\"doi\":\"10.1038/s41467-025-61770-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Rapid movements of plant structures triggered by mechanical force have been documented for centuries; however, how plant cells sense mechanical stimuli and generate rapid response remains unknown. Here we show the central role of a mechanosensitive channel gene in touch-triggered rapid stigma movement of <i>Torenia fournieri</i>. <i>T. fournieri</i> possesses a bilobed stigma sensitive to mechanical stimuli. Using live-cell calcium imaging, we detect that touch induces a wave of cytosolic calcium ([Ca<sup>2+</sup>]<sub>cyt</sub>) essential for stigma movement. Transcriptomic analysis reveals distinct gene expression profiles between the stigma and style, leading to the identification of the <i>MscS-like</i> gene <i>JUE1</i>, predominantly expressed in stigmas. Stigmas of <i>jue1</i> mutants exhibit complete loss of touch-triggered movement, confirming its role as a key regulator in sensitive stigma movement. JUE1 is required for rapid propagation of the touch-induced [Ca<sup>2+</sup>]<sub>cyt</sub>, as cell-to-cell spreading of the [Ca<sup>2+</sup>]<sub>cyt</sub> wave is impaired in the <i>jue1</i>. To conclude, we report a plant mechanosensitive ion channel involved in touch-triggered organ movement by modulating calcium dynamics.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"32 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-61770-6\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-61770-6","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
A mechanosensitive ion channel controls touch-triggered stigma movement through manipulation of calcium signature in Torenia
Rapid movements of plant structures triggered by mechanical force have been documented for centuries; however, how plant cells sense mechanical stimuli and generate rapid response remains unknown. Here we show the central role of a mechanosensitive channel gene in touch-triggered rapid stigma movement of Torenia fournieri. T. fournieri possesses a bilobed stigma sensitive to mechanical stimuli. Using live-cell calcium imaging, we detect that touch induces a wave of cytosolic calcium ([Ca2+]cyt) essential for stigma movement. Transcriptomic analysis reveals distinct gene expression profiles between the stigma and style, leading to the identification of the MscS-like gene JUE1, predominantly expressed in stigmas. Stigmas of jue1 mutants exhibit complete loss of touch-triggered movement, confirming its role as a key regulator in sensitive stigma movement. JUE1 is required for rapid propagation of the touch-induced [Ca2+]cyt, as cell-to-cell spreading of the [Ca2+]cyt wave is impaired in the jue1. To conclude, we report a plant mechanosensitive ion channel involved in touch-triggered organ movement by modulating calcium dynamics.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.