Unveiling the evolution of VIP1 subgroup bZIP transcription factors in plants and the positive effects of BdiVIP1A on heat stress response in Brachypodium distachyon.

IF 4.5 2区 生物学 Q1 PLANT SCIENCES
Min Jiang, Yuxin Zhang, Yiying Liao, Yiqing Gong, Ji Yang
{"title":"Unveiling the evolution of VIP1 subgroup bZIP transcription factors in plants and the positive effects of BdiVIP1A on heat stress response in Brachypodium distachyon.","authors":"Min Jiang, Yuxin Zhang, Yiying Liao, Yiqing Gong, Ji Yang","doi":"10.1007/s00299-025-03572-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Key message: </strong>Plant VIP1 subgroup bZIPs have been characterized, VIP1 orthologs were angiosperm-specific; BdiVIP1A localized in the nucleus and increased plant heat tolerance. In plants, group I basic region/leucine zipper motif (bZIP) transcription factors (TFs), particularly VIP1 and its close homologs (the VIP1 subgroup), play crucial roles in vascular development and osmosensory responses. However, the ancestral origins and evolutionary processes underlying their functional diversity across plant lineages remain poorly understood. In this study, we delve into the origin of VIP1 subgroup bZIP homologs to an ancestral lineage present in charophytes, predating the emergence of land plants. Our phylogenetic analysis identified five distinct clades (A to E), highlighting an early diversification of these genes. Notably, our findings emphasize that VIP1 orthologs represent an angiosperm-specific innovation characterized by dynamic motif gain and/or loss events, as well as relaxed purifying selection, reflecting a unique evolutionary trajectory. Synteny analysis highlights the importance of whole-genome duplication (WGD) events preceding angiosperm divergence in the formation of the bZIP18/bZIP52 group. Codon usage analysis further revealed distinct patterns: monocots exhibited a preference for G3s, C3s, GC3, and overall GC content, whereas dicots showed a tendency toward T3s and A3s. Weighted gene co-expression network analysis (WGCNA) identified a turquoise module significantly associated with the heat stress response, in which BdiVIP1A was identified as a hub gene involved in the response to heat stress in Brachypodium distachyon. Functionally, BdiVIP1A was a nuclear-localized protein that responds to heat stress. Overexpression of BdiVIP1A enhanced thermotolerance by increasing the activity of antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), thereby effectively scavenging reactive oxygen species (ROS). Overall, this research not only elucidates the functional significance of BdiVIP1A in plant responses to heat stress but also deepens our understanding of the evolutionary history of the VIP1 subgroup bZIP homologs. These findings contribute valuable knowledge to ongoing discussions on plant adaptation and survival strategies in the context of global climate change.</p>","PeriodicalId":20204,"journal":{"name":"Plant Cell Reports","volume":"44 8","pages":"179"},"PeriodicalIF":4.5000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Cell Reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00299-025-03572-0","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

Key message: Plant VIP1 subgroup bZIPs have been characterized, VIP1 orthologs were angiosperm-specific; BdiVIP1A localized in the nucleus and increased plant heat tolerance. In plants, group I basic region/leucine zipper motif (bZIP) transcription factors (TFs), particularly VIP1 and its close homologs (the VIP1 subgroup), play crucial roles in vascular development and osmosensory responses. However, the ancestral origins and evolutionary processes underlying their functional diversity across plant lineages remain poorly understood. In this study, we delve into the origin of VIP1 subgroup bZIP homologs to an ancestral lineage present in charophytes, predating the emergence of land plants. Our phylogenetic analysis identified five distinct clades (A to E), highlighting an early diversification of these genes. Notably, our findings emphasize that VIP1 orthologs represent an angiosperm-specific innovation characterized by dynamic motif gain and/or loss events, as well as relaxed purifying selection, reflecting a unique evolutionary trajectory. Synteny analysis highlights the importance of whole-genome duplication (WGD) events preceding angiosperm divergence in the formation of the bZIP18/bZIP52 group. Codon usage analysis further revealed distinct patterns: monocots exhibited a preference for G3s, C3s, GC3, and overall GC content, whereas dicots showed a tendency toward T3s and A3s. Weighted gene co-expression network analysis (WGCNA) identified a turquoise module significantly associated with the heat stress response, in which BdiVIP1A was identified as a hub gene involved in the response to heat stress in Brachypodium distachyon. Functionally, BdiVIP1A was a nuclear-localized protein that responds to heat stress. Overexpression of BdiVIP1A enhanced thermotolerance by increasing the activity of antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), thereby effectively scavenging reactive oxygen species (ROS). Overall, this research not only elucidates the functional significance of BdiVIP1A in plant responses to heat stress but also deepens our understanding of the evolutionary history of the VIP1 subgroup bZIP homologs. These findings contribute valuable knowledge to ongoing discussions on plant adaptation and survival strategies in the context of global climate change.

揭示植物VIP1亚群bZIP转录因子的进化及BdiVIP1A对短柄草热应激反应的积极作用。
关键信息:植物VIP1亚群bZIPs已被鉴定,VIP1同源物是被子植物特有的;BdiVIP1A定位于细胞核,提高了植物的耐热性。在植物中,I组基本区/亮氨酸拉链基序(bZIP)转录因子(TFs),特别是VIP1及其近亲(VIP1亚群)在维管发育和渗透感觉反应中起着至关重要的作用。然而,它们的祖先起源和进化过程在植物谱系中的功能多样性仍然知之甚少。在这项研究中,我们深入研究了VIP1亚群bZIP同源物的起源,该同源物存在于蕨类植物中,早于陆地植物的出现。我们的系统发育分析确定了五个不同的进化支(A到E),突出了这些基因的早期多样化。值得注意的是,我们的研究结果强调,VIP1同源物代表了被子植物特有的创新,其特征是动态的基序获得和/或丧失事件,以及宽松的净化选择,反映了独特的进化轨迹。Synteny分析强调了被子植物分化前的全基因组重复(WGD)事件在bZIP18/bZIP52类群形成中的重要性。密码子使用分析进一步揭示了不同的模式:单子代偏爱G3s、C3s、GC3和总GC含量,而双子代偏爱T3s和A3s。加权基因共表达网络分析(WGCNA)鉴定出一个与热应激反应显著相关的绿松石模块,其中BdiVIP1A被鉴定为短茅(Brachypodium distachyon)中参与热应激反应的枢纽基因。在功能上,BdiVIP1A是一种响应热应激的核定位蛋白。BdiVIP1A的过表达通过增加抗氧化酶如超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)的活性,从而有效清除活性氧(ROS),从而增强了耐热性。总之,本研究不仅阐明了BdiVIP1A在植物热胁迫响应中的功能意义,而且加深了我们对VIP1亚群bZIP同源物的进化史的理解。这些发现为正在进行的关于全球气候变化背景下植物适应和生存策略的讨论提供了宝贵的知识。
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 Cell Reports
Plant Cell Reports 生物-植物科学
CiteScore
10.80
自引率
1.60%
发文量
135
审稿时长
3.2 months
期刊介绍: Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as: - genomics and genetics - metabolism - cell biology - abiotic and biotic stress - phytopathology - gene transfer and expression - molecular pharming - systems biology - nanobiotechnology - genome editing - phenomics and synthetic biology The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.
×
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