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。

IF 8.1 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2025-10-01 DOI:10.1111/nph.70613
Fumika Ikeda,Taku Ohtsubo,Shitomi Nakagawa,Toshiyuki Suzuki,Noriyuki Miyoshi,Emmanuel Vanrobays,Christophe Tatout,Tomoo Shimada,Kentaro Tamura
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引用次数: 0

摘要

十字花科植物的内质网(ER)体通过储存β-葡萄糖苷酶来促进对食草动物的防御,β-葡萄糖苷酶在组织损伤时激活有毒化合物。确保内质网小体结构完整性和酶活性的机制尚不清楚。在这项研究中,我们研究了mid-SUN-POD1复合物在er -体功能中的作用。利用拟南芥(Arabidopsis thaliana) sun3、sun4、sun5三突变体和花粉缺陷基因(POLLEN DEFECTIVE IN GUIDANCE1, POD1)敲低系,我们通过共聚焦显微镜检查了er体形态,通过LC-MS评估了硫代葡萄糖苷的降解,并通过木虱(Armadillidium vulgare)摄食试验评估了食草动物的抗性。sun3、sun4、sun5和pod - 1敲除的植物均表现出内质网体碎片化、组成性内质网胁迫以及对食草动物的敏感性增加,尽管内质网体蛋白正常积累。内质网小体形态缺陷直接损害了这些结构的防御功能,而不影响蛋白质丰度。mid-SUN-POD1复合体对拟南芥内质网体的形态形成和抗草食动物防御至关重要。我们的研究结果证明了这种保守的内质网膜调节系统如何促进内质网衍生的特化细胞器的功能及其在植物防御中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
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.
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