Zeyu Jiang, Kefan Cai, Dongrui Liu, Siting Zhu, Biying Zhao, Jinli Gong, Xuepeng Sun, Meisong Dai, Kai Xu, Xiaolong Li
{"title":"The light-harvesting complex protein LHCB4 fine-tunes temperature-regulated flowering via chloroplast retrograde signaling in pear","authors":"Zeyu Jiang, Kefan Cai, Dongrui Liu, Siting Zhu, Biying Zhao, Jinli Gong, Xuepeng Sun, Meisong Dai, Kai Xu, Xiaolong Li","doi":"10.1093/plphys/kiaf246","DOIUrl":null,"url":null,"abstract":"Flowering is crucial for plant reproductive success and is regulated by both endogenous and external factors. However, the mechanisms by which ambient temperature influences flowering in pear (Pyrus spp.) remain poorly understood. In this study, we observed that elevated temperatures induce early flowering and alter the expression levels of pear light-harvesting complex Lhcb4 (PpyLhcb4) and other flowering-related genes. Notably, the heterologous expression of PpyLhcb4 in Arabidopsis increased chlorophyll content and delayed flowering under normal and high-temperature conditions, suggesting that PpyLhcb4 inhibits flowering by promoting chlorophyll biosynthesis. We also identified a base substitution (A to C) within the PpyLhcb4 promoter region in two pear varieties exhibiting different flowering times. This base substitution affected the CArG-box, which influences PpyLhcb4 promoter activity. Furthermore, the specific binding of the transcription factors PpyAP1 and PpyMADS1 to the PpyLhcb4 promoter was demonstrated. At 22 ℃, PpyLhcb4 expression was not regulated by AP1 but was inhibited by MADS1. However, at 30 ℃, both AP1 and MADS1 upregulated PpyLhcb4 expression. Moreover, we showed that PpyLHCB4 interacts with PpyPIF3 to sense environmental changes. In summary, this study elucidates the molecular mechanisms by which PpyLhcb4 regulates flowering, which involve an intracellular signaling pathway originating from the chloroplast that responds to environmental changes to balance plant growth and development.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"6 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-06-06","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/kiaf246","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 is crucial for plant reproductive success and is regulated by both endogenous and external factors. However, the mechanisms by which ambient temperature influences flowering in pear (Pyrus spp.) remain poorly understood. In this study, we observed that elevated temperatures induce early flowering and alter the expression levels of pear light-harvesting complex Lhcb4 (PpyLhcb4) and other flowering-related genes. Notably, the heterologous expression of PpyLhcb4 in Arabidopsis increased chlorophyll content and delayed flowering under normal and high-temperature conditions, suggesting that PpyLhcb4 inhibits flowering by promoting chlorophyll biosynthesis. We also identified a base substitution (A to C) within the PpyLhcb4 promoter region in two pear varieties exhibiting different flowering times. This base substitution affected the CArG-box, which influences PpyLhcb4 promoter activity. Furthermore, the specific binding of the transcription factors PpyAP1 and PpyMADS1 to the PpyLhcb4 promoter was demonstrated. At 22 ℃, PpyLhcb4 expression was not regulated by AP1 but was inhibited by MADS1. However, at 30 ℃, both AP1 and MADS1 upregulated PpyLhcb4 expression. Moreover, we showed that PpyLHCB4 interacts with PpyPIF3 to sense environmental changes. In summary, this study elucidates the molecular mechanisms by which PpyLhcb4 regulates flowering, which involve an intracellular signaling pathway originating from the chloroplast that responds to environmental changes to balance plant growth and development.
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.