Tianchi Jiang, Wan Zhou, Yiming Ma, Patrick Brown, Lingli Lu
{"title":"Reframing Citrus Iron Deficiency Chlorosis as a Whole-Tree Iron Homeostasis Disorder","authors":"Tianchi Jiang, Wan Zhou, Yiming Ma, Patrick Brown, Lingli Lu","doi":"10.1093/hr/uhag436","DOIUrl":"https://doi.org/10.1093/hr/uhag436","url":null,"abstract":"Iron deficiency chlorosis is a recurrent nutritional disorder that limits citrus growth, productivity and fruit quality, especially in calcareous, saline-alkaline and bicarbonate-rich orchards. Although it is often attributed to poor iron bioavailability in the rhizosphere, its persistence and recurrence cannot be explained by soil chemistry or root uptake alone. Citrus trees are perennial evergreen fruit crops with concurrent sinks, including roots, mature leaves, young flushes, flowers and developing fruits; therefore, iron nutrition depends on rootstock genotype, vascular transport, phloem remobilization, leaf-level iron bioavailability and seasonal source-sink allocation. Here, we reframe citrus iron deficiency chlorosis as a systemic disorder of whole-tree iron homeostasis. We synthesize citrus-specific evidence and broader plant iron-homeostasis concepts to connect rhizosphere iron mobilization, Strategy I root responses, rootstock-mediated acquisition, long-distance transport, the leaf iron paradox, reproductive sink allocation, management strategies and emerging multi-omics approaches. We emphasize that total iron concentration alone is insufficient for diagnosis because iron may be spatially misallocated, chemically immobilized or physiologically unavailable even when bulk levels appear adequate. We further propose a bottleneck-oriented diagnostic workflow linking symptom timing, soil and irrigation constraints, active iron status, root acquisition capacity, vascular transport, spatial localization and confounding stresses to targeted management. This framework provides a crop-specific roadmap for identifying dominant homeostasis bottlenecks, improving iron-efficient rootstock selection and designing precision strategies for recurrent citrus chlorosis.","PeriodicalId":13179,"journal":{"name":"Horticulture Research","volume":"10 1","pages":""},"PeriodicalIF":8.7,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149187923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bin Han, Yanyan Zheng, Jingjing Li, Xuanyu Chen, Minmin Li, Zain Ali, Wenyuan Wang, Yonggang Yin, Shuli Han, Changjiang Liu, Nan Jia, Xinyu Wang, Pingyin Guan, Yan Sun, Yang Liu
{"title":"Grafting-associated chilling tolerance in grapevine involves VvERF113-regulated stilbene biosynthesis and changes in chromatin accessibility","authors":"Bin Han, Yanyan Zheng, Jingjing Li, Xuanyu Chen, Minmin Li, Zain Ali, Wenyuan Wang, Yonggang Yin, Shuli Han, Changjiang Liu, Nan Jia, Xinyu Wang, Pingyin Guan, Yan Sun, Yang Liu","doi":"10.1093/hr/uhag433","DOIUrl":"https://doi.org/10.1093/hr/uhag433","url":null,"abstract":"Grapevine (Vitis vinifera L.) is highly sensitive to low temperature, yet the molecular basis by which rootstocks improve scion chilling tolerance remains poorly understood. Here, we show that the cold-tolerant rootstock CR3 markedly enhances chilling tolerance in the grape cultivar ‘Miguang’. Integrated ATAC-seq and RNA-seq analyses revealed that grafted plants underwent broader chilling-induced changes in chromatin accessibility than self-rooted plants, particularly in genomic regions associated with stress responses and secondary metabolism. Among these pathways, stilbene biosynthesis was strongly activated in grafted plants, accompanied by increased expression of VvSTS genes and higher accumulation of stilbene compounds. Exogenous resveratrol treatment further alleviated chilling-induced damage, supporting a protective role for stilbenes in grapevine chilling adaptation. We further identified the ethylene-responsive transcription factor VvERF113 as a direct repressor of VvSTS expression. Overexpression of VvERF113 suppressed stilbene accumulation and reduced chilling tolerance, whereas RNA interference of VvERF113 promoted stilbene biosynthesis and enhanced chilling tolerance. Together, these findings indicate that repression of VvERF113 in grafted plants may contribute to the enhanced activation of the stilbene pathway associated with CR3 grafting, thereby improving grapevine chilling tolerance, and provide a mechanistic framework for enhancing cold resistance through scion-rootstock interactions.","PeriodicalId":13179,"journal":{"name":"Horticulture Research","volume":"11 1","pages":""},"PeriodicalIF":8.7,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149187920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}