{"title":"等位基因变异和植物结构主要调控因子的交互反馈决定了拟南芥的高海拔适应性。","authors":"Han Zhang,Meng Liu,Shangling Lou,Yu Han,Bao Liu,Songyi Yang,Xiaoqin Feng,Landi Feng,Hao Lin,Yudan Zheng,Yan Song,Jin Yan,Jing Hou,Xuemeng Gao,Shaobo Gu,Yingjun Yao,Xiang Guo,Xuejing Liu,Ruyun Liang,Mengyun Guo,Jianquan Liu,Xiangdong Fu,Huanhuan Liu","doi":"10.1111/nph.70628","DOIUrl":null,"url":null,"abstract":"Ideal plant architectures are crucial for adapting to environmental changes, yet the molecular mechanisms behind high-altitude plant adaptations remain elusive. We characterized the dwarf and highly branched traits of the Tibet ecotype of Arabidopsis thaliana (L.) Heynh. Quantitative trait locus (QTL) analysis revealed that GA5 and BRC1, as major genes regulating plant height and branching, respectively, underlie the variation in plant architecture of the Tibet ecotype. Loss-of-function of GA5 disrupts gibberellin biosynthesis, leading to dwarfism, and natural variations in the BRC1 promoter reduce its expression, promoting branching. A positive feedback loop formed by GA5 and BRC1 via the DELLA-SPL9 module balances plant height and branching. Additionally, alleles of GA5 and BRC1 exhibit contrasting sensitivity to UV-B radiation and low temperatures, suggesting that they have experienced strong ecological selections at high altitudes. Our findings reveal that GA5 and BRC1 form a feedback regulatory module that coordinately regulates the balance between plant height and branching, thereby governing developmental adaptation to high-altitude environments.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"17 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Allelic variations and interactive feedback in major regulators of plant architecture confer high-altitude adaptation in Arabidopsis thaliana.\",\"authors\":\"Han Zhang,Meng Liu,Shangling Lou,Yu Han,Bao Liu,Songyi Yang,Xiaoqin Feng,Landi Feng,Hao Lin,Yudan Zheng,Yan Song,Jin Yan,Jing Hou,Xuemeng Gao,Shaobo Gu,Yingjun Yao,Xiang Guo,Xuejing Liu,Ruyun Liang,Mengyun Guo,Jianquan Liu,Xiangdong Fu,Huanhuan Liu\",\"doi\":\"10.1111/nph.70628\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ideal plant architectures are crucial for adapting to environmental changes, yet the molecular mechanisms behind high-altitude plant adaptations remain elusive. We characterized the dwarf and highly branched traits of the Tibet ecotype of Arabidopsis thaliana (L.) Heynh. Quantitative trait locus (QTL) analysis revealed that GA5 and BRC1, as major genes regulating plant height and branching, respectively, underlie the variation in plant architecture of the Tibet ecotype. Loss-of-function of GA5 disrupts gibberellin biosynthesis, leading to dwarfism, and natural variations in the BRC1 promoter reduce its expression, promoting branching. A positive feedback loop formed by GA5 and BRC1 via the DELLA-SPL9 module balances plant height and branching. Additionally, alleles of GA5 and BRC1 exhibit contrasting sensitivity to UV-B radiation and low temperatures, suggesting that they have experienced strong ecological selections at high altitudes. Our findings reveal that GA5 and BRC1 form a feedback regulatory module that coordinately regulates the balance between plant height and branching, thereby governing developmental adaptation to high-altitude environments.\",\"PeriodicalId\":214,\"journal\":{\"name\":\"New Phytologist\",\"volume\":\"17 1\",\"pages\":\"\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Phytologist\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1111/nph.70628\",\"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":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70628","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Allelic variations and interactive feedback in major regulators of plant architecture confer high-altitude adaptation in Arabidopsis thaliana.
Ideal plant architectures are crucial for adapting to environmental changes, yet the molecular mechanisms behind high-altitude plant adaptations remain elusive. We characterized the dwarf and highly branched traits of the Tibet ecotype of Arabidopsis thaliana (L.) Heynh. Quantitative trait locus (QTL) analysis revealed that GA5 and BRC1, as major genes regulating plant height and branching, respectively, underlie the variation in plant architecture of the Tibet ecotype. Loss-of-function of GA5 disrupts gibberellin biosynthesis, leading to dwarfism, and natural variations in the BRC1 promoter reduce its expression, promoting branching. A positive feedback loop formed by GA5 and BRC1 via the DELLA-SPL9 module balances plant height and branching. Additionally, alleles of GA5 and BRC1 exhibit contrasting sensitivity to UV-B radiation and low temperatures, suggesting that they have experienced strong ecological selections at high altitudes. Our findings reveal that GA5 and BRC1 form a feedback regulatory module that coordinately regulates the balance between plant height and branching, thereby governing developmental adaptation to high-altitude environments.
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.