{"title":"A land plant‐specific VPS13 mediates polarized vesicle trafficking in germinating pollen","authors":"Surachat Tangpranomkorn, Yuka Kimura, Motoko Igarashi, Fumiko Ishizuna, Yoshinobu Kato, Takamasa Suzuki, Takuya Nagae, Sota Fujii, Seiji Takayama","doi":"10.1111/nph.20277","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Pollen has an extraordinary ability to convert from a dry state to an extremely rapidly growing state. During pollination, pollen receives water and Ca<jats:sup>2+</jats:sup> from the contacting pistil, which will be a directional cue for pollen tube germination. The subsequent rapid activation of directional vesicular transport must support the pollen tube growth, but the molecular mechanism leading to this process is largely unknown.</jats:list-item> <jats:list-item>We established a luciferase‐based pollination assay to screen genetic mutants defective in the early stage after pollination. We identified a plant‐specific VPS13, <jats:italic>Arabidopsis thaliana</jats:italic> VPS13a as important for pollen germination, and studied its molecular function.</jats:list-item> <jats:list-item><jats:italic>AtVPS13a</jats:italic> mutation severely affected pollen germination and lipid droplet discharge from the rough endoplasmic reticulum. Cellular accumulation patterns of AtVPS13a and a secretory vesicle marker were synchronized at the polarized site, with a slight delay to the local Ca<jats:sup>2+</jats:sup> elevation. We found a brief Ca<jats:sup>2+</jats:sup> spike after initiation of pollen hydration, which may be related to the directional cues for pollen tube emergence. Although this Ca<jats:sup>2+</jats:sup> dynamics after pollination was unaffected by the absence of AtVPS13a, the mutant suffered reduced cell wall deposition during pollen germination.</jats:list-item> <jats:list-item>AtVPS13a mediates pollen polarization, by regulating proper directional vesicular transport following Ca<jats:sup>2+</jats:sup> signaling for directional tube outgrowth.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"9 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.20277","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
SummaryPollen has an extraordinary ability to convert from a dry state to an extremely rapidly growing state. During pollination, pollen receives water and Ca2+ from the contacting pistil, which will be a directional cue for pollen tube germination. The subsequent rapid activation of directional vesicular transport must support the pollen tube growth, but the molecular mechanism leading to this process is largely unknown.We established a luciferase‐based pollination assay to screen genetic mutants defective in the early stage after pollination. We identified a plant‐specific VPS13, Arabidopsis thaliana VPS13a as important for pollen germination, and studied its molecular function.AtVPS13a mutation severely affected pollen germination and lipid droplet discharge from the rough endoplasmic reticulum. Cellular accumulation patterns of AtVPS13a and a secretory vesicle marker were synchronized at the polarized site, with a slight delay to the local Ca2+ elevation. We found a brief Ca2+ spike after initiation of pollen hydration, which may be related to the directional cues for pollen tube emergence. Although this Ca2+ dynamics after pollination was unaffected by the absence of AtVPS13a, the mutant suffered reduced cell wall deposition during pollen germination.AtVPS13a mediates pollen polarization, by regulating proper directional vesicular transport following Ca2+ signaling for directional tube outgrowth.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.