Tissue-specific expression and genome-wide analysis of RALF gene family in pea (Pisum sativum L.) under different stresses

IF 6.8 Q1 PLANT SCIENCES
Xiwang Xu , Yue Liu , Zhenkun Bai , Li Jia , Chaoran Yu , Mohsin Tanveer , Sergey Shabala , Liping Huang
{"title":"Tissue-specific expression and genome-wide analysis of RALF gene family in pea (Pisum sativum L.) under different stresses","authors":"Xiwang Xu ,&nbsp;Yue Liu ,&nbsp;Zhenkun Bai ,&nbsp;Li Jia ,&nbsp;Chaoran Yu ,&nbsp;Mohsin Tanveer ,&nbsp;Sergey Shabala ,&nbsp;Liping Huang","doi":"10.1016/j.stress.2025.101056","DOIUrl":null,"url":null,"abstract":"<div><div>The rapid alkalinization factor (RALF) gene family plays a crucial role in plant growth, development, and stress responses, yet its characterization in pea (<em>Pisum sativum</em> L.), an agronomically important legume, remains limited. This study identified eight <em>PsRALF</em> genes in the pea genome, phylogenetically clustered into 8 distinct groups, and analyzed their structural features, evolutionary relationships, and expression patterns under various abiotic stresses. Chromosomal localization and collinearity analyses revealed both conserved and lineage-specific duplication events, while promoter analysis identified stress- and hormone-responsive <em>cis</em>-elements, suggesting their roles in stress adaptation. Under abiotic stress conditions such as drought, salinity, and aluminum toxicity, <em>PsRALF2</em> exhibits significant upregulation, highlighting the potential of this gene as a stress-responsive candidate. Subcellular localization predictions indicate that members of this family are predominantly localized extracellularly, with one member targeted to the chloroplast, suggesting that they may possess diverse functional roles. Additionally, All analyzed PsRALFs possesed prion-like domain (PrD) features with varying prominence, suggesting their potential to drive protein aggregation or liquid-liquid phase separation (LLPS) that may mechanistically regulate signaling functions. These findings provide foundational insights into the <em>PsRALF</em> family, offering valuable targets for breeding climate-resilient pea varieties to enhance sustainable agriculture and meet the growing demand for plant-based proteins.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"18 ","pages":"Article 101056"},"PeriodicalIF":6.8000,"publicationDate":"2025-09-25","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/S2667064X25003240","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

The rapid alkalinization factor (RALF) gene family plays a crucial role in plant growth, development, and stress responses, yet its characterization in pea (Pisum sativum L.), an agronomically important legume, remains limited. This study identified eight PsRALF genes in the pea genome, phylogenetically clustered into 8 distinct groups, and analyzed their structural features, evolutionary relationships, and expression patterns under various abiotic stresses. Chromosomal localization and collinearity analyses revealed both conserved and lineage-specific duplication events, while promoter analysis identified stress- and hormone-responsive cis-elements, suggesting their roles in stress adaptation. Under abiotic stress conditions such as drought, salinity, and aluminum toxicity, PsRALF2 exhibits significant upregulation, highlighting the potential of this gene as a stress-responsive candidate. Subcellular localization predictions indicate that members of this family are predominantly localized extracellularly, with one member targeted to the chloroplast, suggesting that they may possess diverse functional roles. Additionally, All analyzed PsRALFs possesed prion-like domain (PrD) features with varying prominence, suggesting their potential to drive protein aggregation or liquid-liquid phase separation (LLPS) that may mechanistically regulate signaling functions. These findings provide foundational insights into the PsRALF family, offering valuable targets for breeding climate-resilient pea varieties to enhance sustainable agriculture and meet the growing demand for plant-based proteins.
不同胁迫下豌豆RALF基因家族的组织特异性表达及全基因组分析
快速碱化因子(RALF)基因家族在植物的生长、发育和逆境响应中起着至关重要的作用,但其在豌豆(Pisum sativum L.)中的特征仍然有限。本研究从豌豆基因组中鉴定出8个PsRALF基因,系统发育聚类为8个不同的类群,分析了它们的结构特征、进化关系以及在不同非生物胁迫下的表达模式。染色体定位和共线性分析揭示了保守的和谱系特异性的重复事件,而启动子分析发现了应激和激素响应的顺式元件,表明它们在应激适应中的作用。在干旱、盐度和铝中毒等非生物胁迫条件下,PsRALF2表现出显著的上调,突出了该基因作为应激反应候选基因的潜力。亚细胞定位预测表明,该家族的成员主要定位于细胞外,其中一个成员定位于叶绿体,这表明它们可能具有多种功能作用。此外,所有分析的PsRALFs都具有不同程度的朊病毒样结构域(PrD)特征,表明它们具有驱动蛋白质聚集或液-液相分离(LLPS)的潜力,可能通过机制调节信号功能。这些发现为PsRALF家族提供了基础见解,为培育适应气候变化的豌豆品种提供了有价值的目标,以促进可持续农业,满足对植物性蛋白质日益增长的需求。
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