{"title":"mid-SUN-POD1复合体确保了拟南芥草食防御所需的内质网体的结构完整性。","authors":"Fumika Ikeda,Taku Ohtsubo,Shitomi Nakagawa,Toshiyuki Suzuki,Noriyuki Miyoshi,Emmanuel Vanrobays,Christophe Tatout,Tomoo Shimada,Kentaro Tamura","doi":"10.1111/nph.70613","DOIUrl":null,"url":null,"abstract":"Specialized endoplasmic reticulum (ER) bodies in Brassicaceae plants facilitate defense against herbivores by storing β-glucosidases that activate toxic compounds upon tissue damage. The mechanisms ensuring the structural integrity and enzymatic activities of the ER body are unknown. In this study, we investigated the role of the mid-SUN-POD1 complex in ER-body function. Using Arabidopsis thaliana sun3 sun4 sun5 triple mutants and POLLEN DEFECTIVE IN GUIDANCE1 (POD1)-knockdown lines, we examined ER-body morphology through confocal microscopy, assessed glucosinolate degradation via LC-MS, and evaluated herbivore resistance through woodlice (Armadillidium vulgare) feeding assays. Both sun3 sun4 sun5 and POD1-knockdown plants exhibited fragmented ER bodies, constitutive ER stress, and increased susceptibility to herbivores, despite normal accumulation of ER-body proteins. The defects in ER-body morphology directly impaired the defense function of these structures rather than affecting protein abundance. The mid-SUN-POD1 complex is critical for ER-body morphogenesis and antiherbivore defense in Arabidopsis. Our findings demonstrate how this conserved ER membrane regulatory system contributes to the function of specialized ER-derived organelles and their role in plant defense.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"69 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The mid-SUN-POD1 complex ensures the structural integrity of ER bodies required for herbivore defense in Arabidopsis.\",\"authors\":\"Fumika Ikeda,Taku Ohtsubo,Shitomi Nakagawa,Toshiyuki Suzuki,Noriyuki Miyoshi,Emmanuel Vanrobays,Christophe Tatout,Tomoo Shimada,Kentaro Tamura\",\"doi\":\"10.1111/nph.70613\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Specialized endoplasmic reticulum (ER) bodies in Brassicaceae plants facilitate defense against herbivores by storing β-glucosidases that activate toxic compounds upon tissue damage. The mechanisms ensuring the structural integrity and enzymatic activities of the ER body are unknown. In this study, we investigated the role of the mid-SUN-POD1 complex in ER-body function. Using Arabidopsis thaliana sun3 sun4 sun5 triple mutants and POLLEN DEFECTIVE IN GUIDANCE1 (POD1)-knockdown lines, we examined ER-body morphology through confocal microscopy, assessed glucosinolate degradation via LC-MS, and evaluated herbivore resistance through woodlice (Armadillidium vulgare) feeding assays. Both sun3 sun4 sun5 and POD1-knockdown plants exhibited fragmented ER bodies, constitutive ER stress, and increased susceptibility to herbivores, despite normal accumulation of ER-body proteins. The defects in ER-body morphology directly impaired the defense function of these structures rather than affecting protein abundance. The mid-SUN-POD1 complex is critical for ER-body morphogenesis and antiherbivore defense in Arabidopsis. Our findings demonstrate how this conserved ER membrane regulatory system contributes to the function of specialized ER-derived organelles and their role in plant defense.\",\"PeriodicalId\":214,\"journal\":{\"name\":\"New Phytologist\",\"volume\":\"69 1\",\"pages\":\"\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-10-01\",\"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.70613\",\"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":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70613","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The mid-SUN-POD1 complex ensures the structural integrity of ER bodies required for herbivore defense in Arabidopsis.
Specialized endoplasmic reticulum (ER) bodies in Brassicaceae plants facilitate defense against herbivores by storing β-glucosidases that activate toxic compounds upon tissue damage. The mechanisms ensuring the structural integrity and enzymatic activities of the ER body are unknown. In this study, we investigated the role of the mid-SUN-POD1 complex in ER-body function. Using Arabidopsis thaliana sun3 sun4 sun5 triple mutants and POLLEN DEFECTIVE IN GUIDANCE1 (POD1)-knockdown lines, we examined ER-body morphology through confocal microscopy, assessed glucosinolate degradation via LC-MS, and evaluated herbivore resistance through woodlice (Armadillidium vulgare) feeding assays. Both sun3 sun4 sun5 and POD1-knockdown plants exhibited fragmented ER bodies, constitutive ER stress, and increased susceptibility to herbivores, despite normal accumulation of ER-body proteins. The defects in ER-body morphology directly impaired the defense function of these structures rather than affecting protein abundance. The mid-SUN-POD1 complex is critical for ER-body morphogenesis and antiherbivore defense in Arabidopsis. Our findings demonstrate how this conserved ER membrane regulatory system contributes to the function of specialized ER-derived organelles and their role in plant defense.
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.