雷帕霉素激酶靶蛋白是植物脂肪酸和脂质合成的正向调节因子

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-12-31 DOI:10.1093/plphys/kiae639
Hui Liu, Jantana Blanford, Hai Shi, Jorg Schwender, John Shanklin, Zhiyang Zhai
{"title":"雷帕霉素激酶靶蛋白是植物脂肪酸和脂质合成的正向调节因子","authors":"Hui Liu, Jantana Blanford, Hai Shi, Jorg Schwender, John Shanklin, Zhiyang Zhai","doi":"10.1093/plphys/kiae639","DOIUrl":null,"url":null,"abstract":"In eukaryotes, Target of Rapamycin (TOR), a conserved protein sensor kinase, integrates diverse environmental cues, including growth factor signals, energy availability, and nutritional status, to direct cell growth. In plants, TOR is activated by light and sugars and regulates a wide range of cellular processes, including protein synthesis and metabolism. Fatty acid synthesis is key to membrane biogenesis that is required for cell growth. To elucidate the primary regulatory role(s) of TOR in lipid metabolism, we followed fatty acid and lipid changes in plants with altered TOR protein levels or activity for short durations, using Nicotiana benthamiana leaves, Arabidopsis seedlings, and Brassica napus cell suspension cultures. Transient expression of TOR significantly elevated the levels of total fatty acids (TFAs) in Nicotiana benthamiana leaves. Conversely, treatment of Arabidopsis seedlings with the TOR-specific inhibitor Torin 2 for one day caused significant reductions in fatty acids and membrane lipids. Similarly, incubating oil-producing Brassica napus suspension culture cells with Torin 2 for eight hours led to significant decreases in the levels of TFAs and triacylglycerol. The results from three independent systems presented here establish that TOR positively regulates lipid synthesis in plants, consistent with its role in animals. Furthermore, RNA-seq analysis of Torin 2-treated Arabidopsis seedlings showed that TOR promotes the upregulation of several genes involved in de novo fatty acid synthesis while downregulating genes involved in lipid turnover, which we propose as a mechanistic explanation for its promotion of lipid synthesis and accumulation.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"12 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Target of Rapamycin kinase is a positive regulator of plant fatty acid and lipid synthesis\",\"authors\":\"Hui Liu, Jantana Blanford, Hai Shi, Jorg Schwender, John Shanklin, Zhiyang Zhai\",\"doi\":\"10.1093/plphys/kiae639\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In eukaryotes, Target of Rapamycin (TOR), a conserved protein sensor kinase, integrates diverse environmental cues, including growth factor signals, energy availability, and nutritional status, to direct cell growth. In plants, TOR is activated by light and sugars and regulates a wide range of cellular processes, including protein synthesis and metabolism. Fatty acid synthesis is key to membrane biogenesis that is required for cell growth. To elucidate the primary regulatory role(s) of TOR in lipid metabolism, we followed fatty acid and lipid changes in plants with altered TOR protein levels or activity for short durations, using Nicotiana benthamiana leaves, Arabidopsis seedlings, and Brassica napus cell suspension cultures. Transient expression of TOR significantly elevated the levels of total fatty acids (TFAs) in Nicotiana benthamiana leaves. Conversely, treatment of Arabidopsis seedlings with the TOR-specific inhibitor Torin 2 for one day caused significant reductions in fatty acids and membrane lipids. Similarly, incubating oil-producing Brassica napus suspension culture cells with Torin 2 for eight hours led to significant decreases in the levels of TFAs and triacylglycerol. The results from three independent systems presented here establish that TOR positively regulates lipid synthesis in plants, consistent with its role in animals. Furthermore, RNA-seq analysis of Torin 2-treated Arabidopsis seedlings showed that TOR promotes the upregulation of several genes involved in de novo fatty acid synthesis while downregulating genes involved in lipid turnover, which we propose as a mechanistic explanation for its promotion of lipid synthesis and accumulation.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2024-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/plphys/kiae639\",\"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":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiae639","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

摘要

在真核生物中,雷帕霉素靶蛋白(TOR)是一种保守的蛋白质传感器激酶,整合多种环境信号,包括生长因子信号、能量可用性和营养状况,来指导细胞生长。在植物中,TOR被光和糖激活,并调节广泛的细胞过程,包括蛋白质合成和代谢。脂肪酸的合成是细胞生长所必需的膜生物发生的关键。为了阐明TOR在脂质代谢中的主要调节作用,我们在短时间内跟踪了TOR蛋白水平或活性改变的植物的脂肪酸和脂质变化,使用了烟叶、拟南芥幼苗和甘蓝型油菜细胞悬浮培养。瞬时表达TOR显著提高了烟叶中总脂肪酸(tfa)的水平。相反,用tor特异性抑制剂Torin 2处理拟南芥幼苗一天,脂肪酸和膜脂显著减少。同样,将产油甘蓝型油菜悬浮培养细胞与Torin 2孵育8小时,tfa和甘油三酯水平显著降低。本文提出的三个独立系统的结果表明,TOR在植物中积极调节脂质合成,与其在动物中的作用一致。此外,对Torin 2处理的拟南芥幼苗的RNA-seq分析显示,TOR促进了几个参与脂肪酸合成的基因的上调,而下调了参与脂质转换的基因,我们认为这是其促进脂质合成和积累的机制解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The Target of Rapamycin kinase is a positive regulator of plant fatty acid and lipid synthesis
In eukaryotes, Target of Rapamycin (TOR), a conserved protein sensor kinase, integrates diverse environmental cues, including growth factor signals, energy availability, and nutritional status, to direct cell growth. In plants, TOR is activated by light and sugars and regulates a wide range of cellular processes, including protein synthesis and metabolism. Fatty acid synthesis is key to membrane biogenesis that is required for cell growth. To elucidate the primary regulatory role(s) of TOR in lipid metabolism, we followed fatty acid and lipid changes in plants with altered TOR protein levels or activity for short durations, using Nicotiana benthamiana leaves, Arabidopsis seedlings, and Brassica napus cell suspension cultures. Transient expression of TOR significantly elevated the levels of total fatty acids (TFAs) in Nicotiana benthamiana leaves. Conversely, treatment of Arabidopsis seedlings with the TOR-specific inhibitor Torin 2 for one day caused significant reductions in fatty acids and membrane lipids. Similarly, incubating oil-producing Brassica napus suspension culture cells with Torin 2 for eight hours led to significant decreases in the levels of TFAs and triacylglycerol. The results from three independent systems presented here establish that TOR positively regulates lipid synthesis in plants, consistent with its role in animals. Furthermore, RNA-seq analysis of Torin 2-treated Arabidopsis seedlings showed that TOR promotes the upregulation of several genes involved in de novo fatty acid synthesis while downregulating genes involved in lipid turnover, which we propose as a mechanistic explanation for its promotion of lipid synthesis and accumulation.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
期刊最新文献
Modifying the TL1-BINDING FACTOR upstream open reading frame coordinates plant growth and defense in rice ATP-CITRATE LYASEB1 supplies materials for sporopollenin biosynthesis and microspore development in Arabidopsis. Enhanced storage lipid biosynthesis promotes somatic embryogenesis in citrus. At5g63290 does not encode coproporphyrinogen III oxidase Surviving Floods: Escape and Quiescence Strategies of Rice Coping with Submergence
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1