{"title":"The Rootstock's Cotyledon-Regulated Fructokinase ClFRK1 Contributes to Graft Union Formation in Watermelon.","authors":"Akebaierjiang Kadeer, Mu Xiong, Chen-le Hou, Bei-Ping Zheng, Hong-Liang Zhang, Xiang-Shuai Wu, Yehia Abouseif, Zu-Hua Zheng, Zhi-Long Bie, Michitaka Notaguchi, Yuan Huang","doi":"10.1111/ppl.70144","DOIUrl":null,"url":null,"abstract":"<p><p>Grafting is a traditional horticultural practice that enhances plant resilience against biotic and abiotic stresses. However, the influence of specific tissues, such as rootstock cotyledons, on graft union formation is not well understood. This study investigates the impact of rootstock cotyledon removal on graft healing in watermelon and its underlying mechanisms. Our results indicate that grafting with rootstock cotyledons (+C) consistently resulted in higher survival rates and better growth outcomes compared to grafting without rootstock cotyledons (-C). This effect was more pronounced in cultivated watermelon rootstocks, which have lower hypocotyl sugar content than wild watermelon rootstocks. Transcriptomic analysis revealed that cotyledon removal disrupted sugar metabolism and affected gene expression related to cell division and tissue development. A fructokinase, ClFRK1, was identified among the candidate genes positively correlated with graft survival rate and healing degree. Silencing ClFRK1 reduced callus proliferation, delayed graft healing and reduced survival rate. Conversely, fructose treatment increased ClFRK1 expression levels at the graft junction, which promoted callus proliferation and vascular reconnection. We propose a novel regulatory model for how ClFRK1 regulates graft union formation. These findings underscore new insights into the interactions and synergistic processes between the graft interface and non-grafted organs during graft union formation and also enrich our understanding of fructokinase.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 2","pages":"e70144"},"PeriodicalIF":5.4000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70144","RegionNum":2,"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
Grafting is a traditional horticultural practice that enhances plant resilience against biotic and abiotic stresses. However, the influence of specific tissues, such as rootstock cotyledons, on graft union formation is not well understood. This study investigates the impact of rootstock cotyledon removal on graft healing in watermelon and its underlying mechanisms. Our results indicate that grafting with rootstock cotyledons (+C) consistently resulted in higher survival rates and better growth outcomes compared to grafting without rootstock cotyledons (-C). This effect was more pronounced in cultivated watermelon rootstocks, which have lower hypocotyl sugar content than wild watermelon rootstocks. Transcriptomic analysis revealed that cotyledon removal disrupted sugar metabolism and affected gene expression related to cell division and tissue development. A fructokinase, ClFRK1, was identified among the candidate genes positively correlated with graft survival rate and healing degree. Silencing ClFRK1 reduced callus proliferation, delayed graft healing and reduced survival rate. Conversely, fructose treatment increased ClFRK1 expression levels at the graft junction, which promoted callus proliferation and vascular reconnection. We propose a novel regulatory model for how ClFRK1 regulates graft union formation. These findings underscore new insights into the interactions and synergistic processes between the graft interface and non-grafted organs during graft union formation and also enrich our understanding of fructokinase.
期刊介绍:
Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.