{"title":"The transcription factor Dof32 coordinates salvianolic acid biosynthesis and drought tolerance in Salvia miltiorrhiza","authors":"Bingbing Lv, Qiaoqiao Feng, Gaige Shao, Anqi Zuo, Xuejiao Yan, Jingying Liu, Juane Dong, Pengda Ma","doi":"10.1093/plphys/kiaf221","DOIUrl":null,"url":null,"abstract":"Drought severely impacts plant growth, yet moderate drought stress can stimulate the biosynthesis of active compounds in medicinal plants. However, the molecular regulators and mechanisms linking drought resistance with the accumulation of active compounds remain poorly understood. In this study, we identified the Dof transcription factor SmDof32 as a key regulator of both salvianolic acid biosynthesis and the drought response in Danshen (Salvia miltiorrhiza). Overexpression of SmDof32 enhanced both the accumulation of medicinal compounds and drought resistance, whereas SmDof32 RNA interference resulted in less accumulation of salvianolic acids and diminished drought tolerance. DNA-affinity purification sequencing (DAP-seq) combined with RNA-sequencing (RNA-seq) analysis revealed that SmDof32 directly promotes the expression of lipoxygenase (SmLOX8) and rosmarinic acid synthase (SmRAS1), thereby increasing the biosynthesis of jasmonic acid (JA) and salvianolic acids. Further analysis of SmLOX8 overexpression and RNAi lines confirmed that SmLOX8 promotes JA biosynthesis, enhances drought tolerance, and increases salvianolic acid biosynthesis. Moreover, inhibition of JA biosynthesis significantly reduced the positive effects of SmDof32 on salvianolic acid accumulation and drought tolerance. Collectively, these findings suggest that the SmDof32-SmLOX8/SmRAS1 module plays a crucial role in the drought response and accumulation of salvianolic acids, providing genetic targets for breeding S. miltiorrhiza with enhanced medicinal compound content and drought resilience.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"54 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-06-03","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/kiaf221","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
Drought severely impacts plant growth, yet moderate drought stress can stimulate the biosynthesis of active compounds in medicinal plants. However, the molecular regulators and mechanisms linking drought resistance with the accumulation of active compounds remain poorly understood. In this study, we identified the Dof transcription factor SmDof32 as a key regulator of both salvianolic acid biosynthesis and the drought response in Danshen (Salvia miltiorrhiza). Overexpression of SmDof32 enhanced both the accumulation of medicinal compounds and drought resistance, whereas SmDof32 RNA interference resulted in less accumulation of salvianolic acids and diminished drought tolerance. DNA-affinity purification sequencing (DAP-seq) combined with RNA-sequencing (RNA-seq) analysis revealed that SmDof32 directly promotes the expression of lipoxygenase (SmLOX8) and rosmarinic acid synthase (SmRAS1), thereby increasing the biosynthesis of jasmonic acid (JA) and salvianolic acids. Further analysis of SmLOX8 overexpression and RNAi lines confirmed that SmLOX8 promotes JA biosynthesis, enhances drought tolerance, and increases salvianolic acid biosynthesis. Moreover, inhibition of JA biosynthesis significantly reduced the positive effects of SmDof32 on salvianolic acid accumulation and drought tolerance. Collectively, these findings suggest that the SmDof32-SmLOX8/SmRAS1 module plays a crucial role in the drought response and accumulation of salvianolic acids, providing genetic targets for breeding S. miltiorrhiza with enhanced medicinal compound content and drought resilience.
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.