Jing Zhang, Ingrid Venables, Damien L Callahan, Alexander B Zwart, John Passioura, Qing Liu, Xue-Rong Zhou, Thomas Vanhercke, Gonzalo M Estavillo
{"title":"水分胁迫通过不同机制促进野生型和转基因高叶油烟甘油三酯的积累","authors":"Jing Zhang, Ingrid Venables, Damien L Callahan, Alexander B Zwart, John Passioura, Qing Liu, Xue-Rong Zhou, Thomas Vanhercke, Gonzalo M Estavillo","doi":"10.1093/plphys/kiaf151","DOIUrl":null,"url":null,"abstract":"Metabolically engineered high-leaf oil plants have been developed to meet the increasing demand for plant oils. Oil production of these plants under controlled conditions is promising; however, their performance under field-like conditions with abiotic stresses remains uncertain. In this study, wild-type (WT) and high-leaf oil (HLO) transgenic tobacco (Nicotiana tabacum) plants were exposed to moderate and sustained water stress to mimic field conditions. The effects of water stress on biomass and lipid accumulation were investigated at the physiological, biochemical, and transcriptional levels. The presence of transgenes increased leaf triacylglycerol (TAG) levels in HLO plants by upregulating endogenous genes involved in lipid biosynthesis at the expense of biomass reduction, altered leaf lipid content and profile, and a decrease in unsaturation levels of membrane lipids compared to WT plants. Moreover, the biomass penalty in HLO plants could reduce canopy transpiration, contributing to their better performance under water-limited environments. Furthermore, WT and HLO plants exhibited enhanced TAG accumulation under water stress but via different mechanisms. In WT plants, water stress induced lipid remodeling, upregulated genes encoding phosphatidic acid phosphatase (PAP), diacylglycerol o-acyltransferase (DGAT2), and lipid droplet-associated proteins (LDAP1), but downregulated genes encoding Gly-Asp-Ser-Leu (GDSL) lipases. In contrast, HLO plants showed increased TAG accumulation primarily through upregulation of OLEOSINS and downregulation of GDSLs under water stress. In conclusion, moderate water stress promoted oil production in HLO plants, demonstrating the robustness of HLO technology for sustainable oil production in the field under water deficit conditions which may be more prevalent in the future due to climate change.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"5 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Water stress enhances triacylglycerol accumulation via different mechanisms in wild-type and transgenic high-leaf oil tobacco\",\"authors\":\"Jing Zhang, Ingrid Venables, Damien L Callahan, Alexander B Zwart, John Passioura, Qing Liu, Xue-Rong Zhou, Thomas Vanhercke, Gonzalo M Estavillo\",\"doi\":\"10.1093/plphys/kiaf151\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Metabolically engineered high-leaf oil plants have been developed to meet the increasing demand for plant oils. Oil production of these plants under controlled conditions is promising; however, their performance under field-like conditions with abiotic stresses remains uncertain. In this study, wild-type (WT) and high-leaf oil (HLO) transgenic tobacco (Nicotiana tabacum) plants were exposed to moderate and sustained water stress to mimic field conditions. The effects of water stress on biomass and lipid accumulation were investigated at the physiological, biochemical, and transcriptional levels. The presence of transgenes increased leaf triacylglycerol (TAG) levels in HLO plants by upregulating endogenous genes involved in lipid biosynthesis at the expense of biomass reduction, altered leaf lipid content and profile, and a decrease in unsaturation levels of membrane lipids compared to WT plants. Moreover, the biomass penalty in HLO plants could reduce canopy transpiration, contributing to their better performance under water-limited environments. Furthermore, WT and HLO plants exhibited enhanced TAG accumulation under water stress but via different mechanisms. In WT plants, water stress induced lipid remodeling, upregulated genes encoding phosphatidic acid phosphatase (PAP), diacylglycerol o-acyltransferase (DGAT2), and lipid droplet-associated proteins (LDAP1), but downregulated genes encoding Gly-Asp-Ser-Leu (GDSL) lipases. In contrast, HLO plants showed increased TAG accumulation primarily through upregulation of OLEOSINS and downregulation of GDSLs under water stress. In conclusion, moderate water stress promoted oil production in HLO plants, demonstrating the robustness of HLO technology for sustainable oil production in the field under water deficit conditions which may be more prevalent in the future due to climate change.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2025-04-12\",\"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/kiaf151\",\"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/kiaf151","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Water stress enhances triacylglycerol accumulation via different mechanisms in wild-type and transgenic high-leaf oil tobacco
Metabolically engineered high-leaf oil plants have been developed to meet the increasing demand for plant oils. Oil production of these plants under controlled conditions is promising; however, their performance under field-like conditions with abiotic stresses remains uncertain. In this study, wild-type (WT) and high-leaf oil (HLO) transgenic tobacco (Nicotiana tabacum) plants were exposed to moderate and sustained water stress to mimic field conditions. The effects of water stress on biomass and lipid accumulation were investigated at the physiological, biochemical, and transcriptional levels. The presence of transgenes increased leaf triacylglycerol (TAG) levels in HLO plants by upregulating endogenous genes involved in lipid biosynthesis at the expense of biomass reduction, altered leaf lipid content and profile, and a decrease in unsaturation levels of membrane lipids compared to WT plants. Moreover, the biomass penalty in HLO plants could reduce canopy transpiration, contributing to their better performance under water-limited environments. Furthermore, WT and HLO plants exhibited enhanced TAG accumulation under water stress but via different mechanisms. In WT plants, water stress induced lipid remodeling, upregulated genes encoding phosphatidic acid phosphatase (PAP), diacylglycerol o-acyltransferase (DGAT2), and lipid droplet-associated proteins (LDAP1), but downregulated genes encoding Gly-Asp-Ser-Leu (GDSL) lipases. In contrast, HLO plants showed increased TAG accumulation primarily through upregulation of OLEOSINS and downregulation of GDSLs under water stress. In conclusion, moderate water stress promoted oil production in HLO plants, demonstrating the robustness of HLO technology for sustainable oil production in the field under water deficit conditions which may be more prevalent in the future due to climate change.
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.