Meta-Analysis of Iron Excess Stress in Rice: Genes and Mechanisms of Tolerance to Acidic Soil.

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Divya Gupta, Sanjib Kumar Panda, Petra Bauer
{"title":"Meta-Analysis of Iron Excess Stress in Rice: Genes and Mechanisms of Tolerance to Acidic Soil.","authors":"Divya Gupta, Sanjib Kumar Panda, Petra Bauer","doi":"10.1111/ppl.70473","DOIUrl":null,"url":null,"abstract":"<p><p>Iron toxicity, predominantly stemming from excessive levels of ferrous iron (Fe<sup>2+</sup>) in acidic soils, poses a considerable challenge for crop production. Hypoxic conditions induced by waterlogging can exacerbate Fe<sup>2+</sup> availability, which significantly impacts the cultivation and productivity of rice (Oryza sativa), a staple food for millions worldwide. In several regions across South America, Africa, and Asia, the prevalence of acidic soils results in elevated Fe<sup>2+</sup> levels leading to iron toxicity, thereby hindering rice yield. Some regional rice varieties demonstrate a notable adaptation to high iron conditions, offering insights into the tolerance mechanisms through comparative physiology and transcriptomic studies. This review synthesizes the various strategies employed by rice plants to mitigate iron toxicity stress, with a focus on the regulation of essential genes and genetic pathways associated with iron transport and homeostasis. We place particular emphasis on the co-expression networks and predicted subcellular localization of the proteins encoded by these genes. A meta-analysis of differential gene expression data gathered from studies involving six distinct rice lines-either tolerant or sensitive-reveals significant influences of plant genotype, developmental stage, and treatment type on the expression patterns, leading to the identification of robust marker genes associated with the iron excess response. Our comprehensive literature review uncovers several critical knowledge gaps, establishing a framework for developing novel approaches aimed at elucidating the molecular mechanisms underpinning iron stress tolerance. These insights are vital for enhancing rice yield in iron-rich, acidic soils, ultimately contributing to improved food security in affected regions.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 5","pages":"e70473"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12391641/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70473","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

Iron toxicity, predominantly stemming from excessive levels of ferrous iron (Fe2+) in acidic soils, poses a considerable challenge for crop production. Hypoxic conditions induced by waterlogging can exacerbate Fe2+ availability, which significantly impacts the cultivation and productivity of rice (Oryza sativa), a staple food for millions worldwide. In several regions across South America, Africa, and Asia, the prevalence of acidic soils results in elevated Fe2+ levels leading to iron toxicity, thereby hindering rice yield. Some regional rice varieties demonstrate a notable adaptation to high iron conditions, offering insights into the tolerance mechanisms through comparative physiology and transcriptomic studies. This review synthesizes the various strategies employed by rice plants to mitigate iron toxicity stress, with a focus on the regulation of essential genes and genetic pathways associated with iron transport and homeostasis. We place particular emphasis on the co-expression networks and predicted subcellular localization of the proteins encoded by these genes. A meta-analysis of differential gene expression data gathered from studies involving six distinct rice lines-either tolerant or sensitive-reveals significant influences of plant genotype, developmental stage, and treatment type on the expression patterns, leading to the identification of robust marker genes associated with the iron excess response. Our comprehensive literature review uncovers several critical knowledge gaps, establishing a framework for developing novel approaches aimed at elucidating the molecular mechanisms underpinning iron stress tolerance. These insights are vital for enhancing rice yield in iron-rich, acidic soils, ultimately contributing to improved food security in affected regions.

Abstract Image

Abstract Image

Abstract Image

水稻铁胁迫的荟萃分析:耐酸性土壤的基因和机制。
铁毒性主要是由酸性土壤中亚铁(Fe2+)含量过高引起的,对作物生产构成了相当大的挑战。涝渍引起的缺氧条件会加剧Fe2+的有效性,从而显著影响水稻(Oryza sativa)的种植和生产力,而水稻是全球数百万人的主食。在南美洲、非洲和亚洲的一些地区,酸性土壤的普遍存在导致铁离子水平升高,从而导致铁中毒,从而阻碍水稻产量。一些区域水稻品种表现出对高铁条件的显著适应,通过比较生理学和转录组学研究提供了对耐铁机制的见解。本文综述了水稻植物减轻铁毒性胁迫的各种策略,重点介绍了与铁转运和体内平衡相关的必需基因和遗传途径的调控。我们特别强调共表达网络和预测这些基因编码的蛋白质的亚细胞定位。对6个不同水稻品系(包括耐受性和敏感性)的差异基因表达数据进行荟萃分析,揭示了植物基因型、发育阶段和处理类型对表达模式的显著影响,从而确定了与铁过量反应相关的稳健标记基因。我们的综合文献综述揭示了几个关键的知识空白,建立了一个框架,开发新的方法,旨在阐明铁胁迫耐受的分子机制。这些见解对于提高富铁酸性土壤中的水稻产量至关重要,最终有助于改善受影响地区的粮食安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信