Juan Yang,Guoqiang Xu,Mingyue Zhang,Weicong Xue,Jie Wu,Yilin Li,Guangshu Song,Baobao Wang,Yongming Liu,Xiaoyuan Chen,Dexin Kong,Haiyang Wang
{"title":"Dual role of Gloosy15 in regulating flowering by modulating gibberellins and floral organ gene expression in maize.","authors":"Juan Yang,Guoqiang Xu,Mingyue Zhang,Weicong Xue,Jie Wu,Yilin Li,Guangshu Song,Baobao Wang,Yongming Liu,Xiaoyuan Chen,Dexin Kong,Haiyang Wang","doi":"10.1111/nph.70492","DOIUrl":null,"url":null,"abstract":"Flowering time is determined by two developmental transitions (vegetative phase change and floral transition), and is a key determinant of maize adaptation and yield potential. Gloosy15 (Gl15) encodes an APETALA2 (AP2)-like transcription factor that negatively regulates maize vegetative phase change. However, the underlying explicit molecular mechanism of Gl15 remains unclear. In this study, we report that Gl15 is a candidate quantitative trait locus (QTL) for vegetative phase change and a selective target during modern maize breeding, and demonstrate that the Hap1 allele of Gl15 likely represents a favorable haplotype under selection for early flowering. We show that Gl15 directly downregulates the expression of a gibberellin (GA) biosynthesis gene (DWARF1, D1), but upregulates the expression of a GA catabolism gene (ZmGA2ox3) in both the leaf and shoot apices, leading to reduced bioactive GA levels and delayed flowering. We also find that Gl15 directly inhibits the expression of the floral activator ZMM4 in the shoot apex to delay floral transition. Our findings suggest a dual role of Gl15 in regulating flowering by modulating gibberellins and floral organ gene expression in maize, and provide new genetic targets for improving flowering time in maize cultivars.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"81 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-09-21","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.70492","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
Flowering time is determined by two developmental transitions (vegetative phase change and floral transition), and is a key determinant of maize adaptation and yield potential. Gloosy15 (Gl15) encodes an APETALA2 (AP2)-like transcription factor that negatively regulates maize vegetative phase change. However, the underlying explicit molecular mechanism of Gl15 remains unclear. In this study, we report that Gl15 is a candidate quantitative trait locus (QTL) for vegetative phase change and a selective target during modern maize breeding, and demonstrate that the Hap1 allele of Gl15 likely represents a favorable haplotype under selection for early flowering. We show that Gl15 directly downregulates the expression of a gibberellin (GA) biosynthesis gene (DWARF1, D1), but upregulates the expression of a GA catabolism gene (ZmGA2ox3) in both the leaf and shoot apices, leading to reduced bioactive GA levels and delayed flowering. We also find that Gl15 directly inhibits the expression of the floral activator ZMM4 in the shoot apex to delay floral transition. Our findings suggest a dual role of Gl15 in regulating flowering by modulating gibberellins and floral organ gene expression in maize, and provide new genetic targets for improving flowering time in maize cultivars.
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.