V0 and V1 domains of vacuolar H+-ATPase play distinct roles in cadmium tolerance of Broussonetia papyrifera.

IF 3.4 3区 生物学 Q1 PLANT SCIENCES
Plant Biology Pub Date : 2026-09-21 DOI:10.1111/plb.70292
W Tianyu, J Yuying, H Yani, T Xingjing, K Aleem, Y Le, L Peiwei, N R Shahi, X Zhenggang, Y Guiyan
{"title":"V<sub>0</sub> and V<sub>1</sub> domains of vacuolar H<sup>+</sup>-ATPase play distinct roles in cadmium tolerance of Broussonetia papyrifera.","authors":"W Tianyu, J Yuying, H Yani, T Xingjing, K Aleem, Y Le, L Peiwei, N R Shahi, X Zhenggang, Y Guiyan","doi":"10.1111/plb.70292","DOIUrl":null,"url":null,"abstract":"<p><p>Cadmium (Cd) contamination poses a major threat to forest ecosystems, and Broussonetia papyrifera is a promising woody species with strong Cd tolerance and accumulation capacity. Vacuolar H<sup>+</sup>-ATPase (V-ATPase) is central to ion homeostasis and heavy metal detoxification, yet the organ- and domain-specific roles of its subunits in Cd responses remain unclear. We integrated physiological measurements, transcript profiling, enzyme activity assays and genome-wide analyses to characterize V-ATPase subunits (BpVHAs) and their functions under a 30-day Cd treatment in roots, stems and leaves of B. papyrifera. Cd stress caused only mild electrolyte leakage but triggered substantial V-ATPase accumulation and enhanced activity. V-ATPase activity displayed a tissue-graded temporal pattern, with roots responding earliest and most strongly. We identified 22 BpVHA genes belonging to conserved V<sub>0</sub> and V<sub>1</sub> domains, whose promoters were enriched in stress- and hormone-related cis-elements. Most genes exhibited a rise-then-fall expression trend during Cd exposure, with V<sub>0</sub> subunits induced earlier, more strongly and for longer than V<sub>1</sub> subunits. Mantel tests showed that V<sub>1</sub> expression correlated more strongly with V-ATPase activity in roots, whereas V<sub>0</sub> expression dominated in stems and leaves. Our findings highlight BpVHA-a2, BpVHA-a3 and BpVHA-c1 as key contributors to Cd detoxification. We propose a model in which roots rely on rapid V<sub>1</sub>-driven ATP hydrolysis, while aerial tissues depend on sustained V<sub>0</sub>-mediated proton pumping to support vacuolar Cd sequestration. This study provides new insights into heavy metal tolerance in woody plants and identifies promising molecular targets for breeding and phytoremediation in Cd-contaminated environments.</p>","PeriodicalId":220,"journal":{"name":"Plant Biology","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2026-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/plb.70292","RegionNum":3,"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

Cadmium (Cd) contamination poses a major threat to forest ecosystems, and Broussonetia papyrifera is a promising woody species with strong Cd tolerance and accumulation capacity. Vacuolar H+-ATPase (V-ATPase) is central to ion homeostasis and heavy metal detoxification, yet the organ- and domain-specific roles of its subunits in Cd responses remain unclear. We integrated physiological measurements, transcript profiling, enzyme activity assays and genome-wide analyses to characterize V-ATPase subunits (BpVHAs) and their functions under a 30-day Cd treatment in roots, stems and leaves of B. papyrifera. Cd stress caused only mild electrolyte leakage but triggered substantial V-ATPase accumulation and enhanced activity. V-ATPase activity displayed a tissue-graded temporal pattern, with roots responding earliest and most strongly. We identified 22 BpVHA genes belonging to conserved V0 and V1 domains, whose promoters were enriched in stress- and hormone-related cis-elements. Most genes exhibited a rise-then-fall expression trend during Cd exposure, with V0 subunits induced earlier, more strongly and for longer than V1 subunits. Mantel tests showed that V1 expression correlated more strongly with V-ATPase activity in roots, whereas V0 expression dominated in stems and leaves. Our findings highlight BpVHA-a2, BpVHA-a3 and BpVHA-c1 as key contributors to Cd detoxification. We propose a model in which roots rely on rapid V1-driven ATP hydrolysis, while aerial tissues depend on sustained V0-mediated proton pumping to support vacuolar Cd sequestration. This study provides new insights into heavy metal tolerance in woody plants and identifies promising molecular targets for breeding and phytoremediation in Cd-contaminated environments.

液泡H+- atp酶V0和V1结构域在纸莎草耐镉性中起着不同的作用。
镉(Cd)污染是森林生态系统的主要威胁,纸莎草(Broussonetia papyrifera)具有较强的Cd耐受性和积累能力,是一种有发展前途的木本树种。液泡H+- atp酶(v - atp酶)是离子稳态和重金属解毒的核心,但其亚基在Cd反应中的器官和领域特异性作用尚不清楚。我们综合了生理测量、转录谱分析、酶活性分析和全基因组分析来表征纸莎草根、茎和叶在30天Cd处理下的v - atp酶亚基(BpVHAs)及其功能。镉胁迫仅引起轻度电解质泄漏,但引起v - atp酶大量积累和活性增强。v - atp酶活性表现出组织分级的时间模式,根反应最早,最强烈。我们鉴定出22个BpVHA基因属于保守的V0和V1结构域,其启动子富含应激和激素相关的顺式元件。大多数基因在Cd暴露过程中表现出先上升后下降的表达趋势,其中V0亚基比V1亚基更早、更强、持续时间更长。Mantel试验表明,在根中V1的表达与V-ATPase活性的相关性更强,而在茎和叶中V0的表达占主导地位。我们的研究结果强调BpVHA-a2, BpVHA-a3和BpVHA-c1是Cd解毒的关键贡献者。我们提出了一个模型,其中根依赖于快速的v1驱动的ATP水解,而空中组织依赖于持续的v0介导的质子泵送来支持液泡Cd封存。该研究为木本植物的重金属耐受性提供了新的见解,并为cd污染环境中的育种和植物修复确定了有希望的分子靶点。
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 Biology
Plant Biology 生物-植物科学
CiteScore
8.20
自引率
2.60%
发文量
109
审稿时长
3 months
期刊介绍: Plant Biology is an international journal of broad scope bringing together the different subdisciplines, such as physiology, molecular biology, cell biology, development, genetics, systematics, ecology, evolution, ecophysiology, plant-microbe interactions, and mycology. Plant Biology publishes original problem-oriented full-length research papers, short research papers, and review articles. Discussion of hot topics and provocative opinion articles are published under the heading Acute Views. From a multidisciplinary perspective, Plant Biology will provide a platform for publication, information and debate, encompassing all areas which fall within the scope of plant science.
×
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
小红书