Erlin Gao, Yunju Zhao, Mengxia Wu, Kun Wang, Qiwei Zheng, Yanlong Li, Xiaolu Qu, Xiaomeng Wu, Wenwu Guo, Pengwei Wang
{"title":"Autophagy is essential for somatic embryogenesis in citrus through regulating amyloplast degradation and lipid homeostasis","authors":"Erlin Gao, Yunju Zhao, Mengxia Wu, Kun Wang, Qiwei Zheng, Yanlong Li, Xiaolu Qu, Xiaomeng Wu, Wenwu Guo, Pengwei Wang","doi":"10.1111/nph.20242","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n </p><ul>\n \n <li>Autophagy is a conserved degradation pathway that regulates the clearance of paternal substrate at the early embryogenesis stage of animals. However, its mode of action is likely different in plants, which can regenerate through apomixis without fertilisation.</li>\n \n <li>Somatic embryogenesis (SE) is a unique plant process widely used for plant propagation and germplasm utilisation. Here, we studied citrus as an example and found a higher autophagic activity after SE initiation. Interestingly, amyloplasts were frequently found inside autophagosomes, whereas the inhibition of autophagy blocks amyloplasts/starch degradation and hinders somatic embryo formation.</li>\n \n <li>Furthermore, the consumption of storage lipids was faster in autophagy mutants, suggesting lipid metabolism is activated when starch utilisation is blocked. Exogenous application of autophagy-inducing chemicals (e.g. spermidine) significantly promoted the formation of autophagosomes and increased SE efficiency, indicating a positive correlation between autophagy, energy metabolism, and somatic embryo formation in citrus.</li>\n \n <li>Taken together, our study unveils a pathway for the degradation of plant-specific organelles and provides an effective approach for plant propagation.</li>\n </ul>\n </div>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"245 2","pages":"684-697"},"PeriodicalIF":8.3000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/nph.20242","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
Autophagy is a conserved degradation pathway that regulates the clearance of paternal substrate at the early embryogenesis stage of animals. However, its mode of action is likely different in plants, which can regenerate through apomixis without fertilisation.
Somatic embryogenesis (SE) is a unique plant process widely used for plant propagation and germplasm utilisation. Here, we studied citrus as an example and found a higher autophagic activity after SE initiation. Interestingly, amyloplasts were frequently found inside autophagosomes, whereas the inhibition of autophagy blocks amyloplasts/starch degradation and hinders somatic embryo formation.
Furthermore, the consumption of storage lipids was faster in autophagy mutants, suggesting lipid metabolism is activated when starch utilisation is blocked. Exogenous application of autophagy-inducing chemicals (e.g. spermidine) significantly promoted the formation of autophagosomes and increased SE efficiency, indicating a positive correlation between autophagy, energy metabolism, and somatic embryo formation in citrus.
Taken together, our study unveils a pathway for the degradation of plant-specific organelles and provides an effective approach for plant propagation.
自噬是一种保守的降解途径,可在动物早期胚胎发生阶段调节父系基质的清除。然而,自噬的作用模式在植物中可能有所不同,因为植物可以通过无性繁殖进行再生,而无需受精。体细胞胚胎发生(SE)是一种独特的植物过程,广泛用于植物繁殖和种质利用。在此,我们以柑橘为例进行了研究,发现体细胞胚胎发生后自噬活性较高。有趣的是,淀粉体经常出现在自噬体中,而抑制自噬会阻止淀粉体/淀粉降解,阻碍体细胞胚胎的形成。此外,自噬突变体中储存脂质的消耗更快,这表明当淀粉利用受阻时,脂质代谢被激活。外源应用自噬诱导化学物质(如亚精胺)可显著促进自噬体的形成并提高 SE 的效率,这表明柑橘的自噬、能量代谢和体细胞胚胎形成之间存在正相关。综上所述,我们的研究揭示了植物特有细胞器的降解途径,为植物繁殖提供了一种有效的方法。
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.