{"title":"姜黄调节器官分化和休眠的转录景观和动态","authors":"Xuezhu Liao, Mengmeng Hou, Yixuan Liu, Bing Xu, Xiaolong Huang, Christophe Bailly, Minlong Jia, Tengbo Huang, Zhiqiang Wu","doi":"10.1093/plphys/kiaf501","DOIUrl":null,"url":null,"abstract":"The emergence of specialized organs represents key evolutionary innovations that enable plants to thrive in diverse environments. However, the developmental mechanisms underlying these traits, particularly those of underground storage organs like rhizomes, remain poorly understood. Siam tulip (Curcuma alismatifolia Gagnep.), with its unique suite of modified organs (such as bracts, rhizomes, and tuberous roots) and dual reproductive strategies through seeds and rhizomes, serves as an ideal model for exploring organ differentiation and dormancy regulation. Through a comprehensive organ-wide transcriptomic analysis, we revealed functional differentiation and conservation across C. alismatifolia organs. For example, the outer bracts retain photosynthetic capacity similar to leaves, while the inner bracts have lost this function. The rhizome, a critical reproductive organ, acts as both a nutrient reservoir and a dormancy-driven survival mechanism in adverse conditions. Using Weighted Gene Co-expression Network Analysis (WGCNA), we identified transcription factors associated with ABRE cis-acting elements as key regulators of rhizome development. By integrating transcriptomic data with high-temperature and phytohormone treatments, heterologous expression, dual-luciferase reporter assays and yeast one-hybrid assays, we demonstrated the central role of cytochrome P450 (P450) genes, particularly ABA 8’-hydroxylase 1 (CYP707A1), in regulating rhizome dormancy release and high-temperature responses. Moreover, we showed that CYP707A1 is regulated by the MYB transcription factor 96 (MYB96), WRKY transcription factor 35 (WRKY35), AP2/ERF and B3 domain-containing transcription factor RAV1 (RAV1), and Two-component response regulator ARR18 (ARR18) transcription factors, offering potential strategies for year-round production. This study establishes C. alismatifolia as a powerful model for investigating the formation and specialization of evolutionary innovations like rhizomes and bracts, highlighting their adaptive mechanisms and resilience to environmental challenges in Zingiberaceae.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"182 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The transcriptional landscape and dynamics regulating organ differentiation and dormancy in Curcuma alismatifolia\",\"authors\":\"Xuezhu Liao, Mengmeng Hou, Yixuan Liu, Bing Xu, Xiaolong Huang, Christophe Bailly, Minlong Jia, Tengbo Huang, Zhiqiang Wu\",\"doi\":\"10.1093/plphys/kiaf501\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The emergence of specialized organs represents key evolutionary innovations that enable plants to thrive in diverse environments. However, the developmental mechanisms underlying these traits, particularly those of underground storage organs like rhizomes, remain poorly understood. Siam tulip (Curcuma alismatifolia Gagnep.), with its unique suite of modified organs (such as bracts, rhizomes, and tuberous roots) and dual reproductive strategies through seeds and rhizomes, serves as an ideal model for exploring organ differentiation and dormancy regulation. Through a comprehensive organ-wide transcriptomic analysis, we revealed functional differentiation and conservation across C. alismatifolia organs. For example, the outer bracts retain photosynthetic capacity similar to leaves, while the inner bracts have lost this function. The rhizome, a critical reproductive organ, acts as both a nutrient reservoir and a dormancy-driven survival mechanism in adverse conditions. Using Weighted Gene Co-expression Network Analysis (WGCNA), we identified transcription factors associated with ABRE cis-acting elements as key regulators of rhizome development. By integrating transcriptomic data with high-temperature and phytohormone treatments, heterologous expression, dual-luciferase reporter assays and yeast one-hybrid assays, we demonstrated the central role of cytochrome P450 (P450) genes, particularly ABA 8’-hydroxylase 1 (CYP707A1), in regulating rhizome dormancy release and high-temperature responses. Moreover, we showed that CYP707A1 is regulated by the MYB transcription factor 96 (MYB96), WRKY transcription factor 35 (WRKY35), AP2/ERF and B3 domain-containing transcription factor RAV1 (RAV1), and Two-component response regulator ARR18 (ARR18) transcription factors, offering potential strategies for year-round production. This study establishes C. alismatifolia as a powerful model for investigating the formation and specialization of evolutionary innovations like rhizomes and bracts, highlighting their adaptive mechanisms and resilience to environmental challenges in Zingiberaceae.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"182 1\",\"pages\":\"\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-10-13\",\"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/kiaf501\",\"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/kiaf501","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The transcriptional landscape and dynamics regulating organ differentiation and dormancy in Curcuma alismatifolia
The emergence of specialized organs represents key evolutionary innovations that enable plants to thrive in diverse environments. However, the developmental mechanisms underlying these traits, particularly those of underground storage organs like rhizomes, remain poorly understood. Siam tulip (Curcuma alismatifolia Gagnep.), with its unique suite of modified organs (such as bracts, rhizomes, and tuberous roots) and dual reproductive strategies through seeds and rhizomes, serves as an ideal model for exploring organ differentiation and dormancy regulation. Through a comprehensive organ-wide transcriptomic analysis, we revealed functional differentiation and conservation across C. alismatifolia organs. For example, the outer bracts retain photosynthetic capacity similar to leaves, while the inner bracts have lost this function. The rhizome, a critical reproductive organ, acts as both a nutrient reservoir and a dormancy-driven survival mechanism in adverse conditions. Using Weighted Gene Co-expression Network Analysis (WGCNA), we identified transcription factors associated with ABRE cis-acting elements as key regulators of rhizome development. By integrating transcriptomic data with high-temperature and phytohormone treatments, heterologous expression, dual-luciferase reporter assays and yeast one-hybrid assays, we demonstrated the central role of cytochrome P450 (P450) genes, particularly ABA 8’-hydroxylase 1 (CYP707A1), in regulating rhizome dormancy release and high-temperature responses. Moreover, we showed that CYP707A1 is regulated by the MYB transcription factor 96 (MYB96), WRKY transcription factor 35 (WRKY35), AP2/ERF and B3 domain-containing transcription factor RAV1 (RAV1), and Two-component response regulator ARR18 (ARR18) transcription factors, offering potential strategies for year-round production. This study establishes C. alismatifolia as a powerful model for investigating the formation and specialization of evolutionary innovations like rhizomes and bracts, highlighting their adaptive mechanisms and resilience to environmental challenges in Zingiberaceae.
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.