OsNRAMP7 positively regulates heat tolerance at seedling and reproductive stages in rice

IF 6.8 Q1 PLANT SCIENCES
Jingfang Dong , Ke Chen , Luo Chen, Minhua Zheng, Shuai Nie, Chanjuan Ye, Xuezhong Li, Guowei Xie, Hao Chen, Junliang Zhao, Song Bai, Wu Yang
{"title":"OsNRAMP7 positively regulates heat tolerance at seedling and reproductive stages in rice","authors":"Jingfang Dong ,&nbsp;Ke Chen ,&nbsp;Luo Chen,&nbsp;Minhua Zheng,&nbsp;Shuai Nie,&nbsp;Chanjuan Ye,&nbsp;Xuezhong Li,&nbsp;Guowei Xie,&nbsp;Hao Chen,&nbsp;Junliang Zhao,&nbsp;Song Bai,&nbsp;Wu Yang","doi":"10.1016/j.stress.2025.100870","DOIUrl":null,"url":null,"abstract":"<div><div>Heat stress is a significant environmental threat that affects the growth and productivity of rice. However, there is currently limited understanding of heat tolerance. Natural resistance-associated macrophage proteins (NRAMPs) are known for their roles in ions uptake, transportation, and disease resistance, but their role in heat resistance is still unknown. In this study, we demonstrated that <em>OsNRAMP7</em>, a member of the <em>NRAMP</em> family in rice, positively regulates heat resistance at both vegetative and reproductive stages by generation of knockout and overexpression transgenic lines. <em>OsNRAMP7</em> was highly expressed in leaf blades, roots, immature panicles, flag leaf sheaths, and husks. The expression of <em>OsNRAMP7</em> was strongly induced in rice shoots when exposed to heat stress. Under heat stress, <em>OsNRAMP7</em> knockout plants exhibited more severe leaf damage and lower survival rates at the seedling stage, and decreased seed-setting rates and seed weight per plant at the reproductive stage compared to the wild type. Conversely, the <em>OsNRAMP7</em> overexpression plants exhibited enhanced heat tolerance across these phenotypic parameters. OsNRAMP7 is co-localized in the <em>Endoplasmic Reticulum</em> and Golgi. Transcriptome analysis revealed significant changes in the ribosome pathway in transgenic plants under heat stress. The <em>OsNRAMP7</em> overexpression plants increased the total antioxidant capacity and water content in rice after heat stress, and exhibited stronger heat tolerance. There are three main distinct haplotypes of <em>OsNRAMP7</em> in natural populations that are unevenly distributed across various cultivated rice regions and showed differentiation among subpopulations. This study reports for the first time the biological function of <em>NRAMP</em> family member <em>OsNRAMP7</em> in heat tolerance and lays the foundation for expanding the molecular regulation mechanism of heat tolerance in rice.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"16 ","pages":"Article 100870"},"PeriodicalIF":6.8000,"publicationDate":"2025-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X25001381","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Heat stress is a significant environmental threat that affects the growth and productivity of rice. However, there is currently limited understanding of heat tolerance. Natural resistance-associated macrophage proteins (NRAMPs) are known for their roles in ions uptake, transportation, and disease resistance, but their role in heat resistance is still unknown. In this study, we demonstrated that OsNRAMP7, a member of the NRAMP family in rice, positively regulates heat resistance at both vegetative and reproductive stages by generation of knockout and overexpression transgenic lines. OsNRAMP7 was highly expressed in leaf blades, roots, immature panicles, flag leaf sheaths, and husks. The expression of OsNRAMP7 was strongly induced in rice shoots when exposed to heat stress. Under heat stress, OsNRAMP7 knockout plants exhibited more severe leaf damage and lower survival rates at the seedling stage, and decreased seed-setting rates and seed weight per plant at the reproductive stage compared to the wild type. Conversely, the OsNRAMP7 overexpression plants exhibited enhanced heat tolerance across these phenotypic parameters. OsNRAMP7 is co-localized in the Endoplasmic Reticulum and Golgi. Transcriptome analysis revealed significant changes in the ribosome pathway in transgenic plants under heat stress. The OsNRAMP7 overexpression plants increased the total antioxidant capacity and water content in rice after heat stress, and exhibited stronger heat tolerance. There are three main distinct haplotypes of OsNRAMP7 in natural populations that are unevenly distributed across various cultivated rice regions and showed differentiation among subpopulations. This study reports for the first time the biological function of NRAMP family member OsNRAMP7 in heat tolerance and lays the foundation for expanding the molecular regulation mechanism of heat tolerance in rice.
OsNRAMP7正调控水稻苗期和生殖期的耐热性
热胁迫是影响水稻生长和生产力的重要环境威胁。然而,目前对耐热性的了解有限。天然抗性相关巨噬细胞蛋白(NRAMPs)因其在离子摄取、运输和抗病性中的作用而闻名,但其在耐热性中的作用尚不清楚。在这项研究中,我们证明了OsNRAMP7是水稻NRAMP家族的成员,通过产生敲除和过表达转基因株系,在营养和生殖阶段都积极调节耐热性。OsNRAMP7在叶片、根、未成熟穗、旗叶鞘和壳中高度表达。OsNRAMP7的表达在高温胁迫下受到强烈诱导。在高温胁迫下,OsNRAMP7基因敲除植株幼苗期叶片损伤更严重,成活率更低,生殖期结实率和单株种子重也比野生型低。相反,OsNRAMP7过表达植株在这些表型参数中表现出更强的耐热性。OsNRAMP7共定位于内质网和高尔基体。转录组分析显示转基因植物在高温胁迫下核糖体途径发生了显著变化。OsNRAMP7过表达植株增加了水稻热胁迫后的总抗氧化能力和水分含量,表现出更强的耐热性。OsNRAMP7在自然居群中主要有三种不同的单倍型,它们在不同水稻栽培区域分布不均匀,并在亚居群中表现出分化。本研究首次报道了NRAMP家族成员OsNRAMP7在耐热性中的生物学功能,为拓展水稻耐热性的分子调控机制奠定了基础。
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
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
×
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