小麦4-Coumarate-CoA连接酶基因家族的全基因组分析:盐胁迫和光调节冷驯化下的表达模式

IF 6.8 Q1 PLANT SCIENCES
Fatemeh Gholizadeh, Gabriella Szalai, Tibor Janda
{"title":"小麦4-Coumarate-CoA连接酶基因家族的全基因组分析:盐胁迫和光调节冷驯化下的表达模式","authors":"Fatemeh Gholizadeh,&nbsp;Gabriella Szalai,&nbsp;Tibor Janda","doi":"10.1016/j.stress.2025.100879","DOIUrl":null,"url":null,"abstract":"<div><div>The 4-coumarate-CoA ligase (<em>4CL</em>) gene family plays a fundamental role in the phenylpropanoid pathway, influencing plant growth, lignin biosynthesis, and stress adaptation. Despite its significance, the <em>4CL</em> gene family in wheat (<em>T. aestivum</em> L.) has not been extensively studied. This study identified 40 <em>Ta4CL</em> genes distributed across 20 chromosomes, characterizing their structural features, phylogenetic relationships, and subcellular localization. Promoter analysis revealed cis-regulatory elements linked to stress response, hormone signaling, and light regulation. Gene expression analysis demonstrated that specific <em>Ta4CL</em> genes, such as <em>Ta4CL8–5A</em> and <em>Ta4CL4–7D</em>, were significantly upregulated under high salinity conditions, indicating their role in salt tolerance. Additionally, light-regulated cold acclimation experiments showed differential expression of multiple <em>Ta4CL</em> genes, with <em>Ta4CL2–6D</em> and <em>Ta4CL3–6B</em> displaying notable induction under blue light and cold stress. Protein interaction analysis highlighted the involvement of Ta4CLs in lignin and flavonoid biosynthesis, particularly through interactions with phenylalanine ammonia-lyase and other key enzymes in the phenylpropanoid pathway. Physiological assessments confirmed that Na<sup>+</sup> accumulation and the Na<sup>+</sup>/<em>K</em><sup>+</sup> ratio were correlated with the expression of specific <em>Ta4CL</em> genes, reinforcing their functional role in stress adaptation. These findings provide valuable insights into the diverse roles of <em>4CL</em> genes and offer potential targets for breeding stress-resilient wheat cultivars.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"16 ","pages":"Article 100879"},"PeriodicalIF":6.8000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genome-wide analysis of the 4-Coumarate-CoA ligase gene family in wheat: Expression patterns under salt stress and light-regulated cold acclimation\",\"authors\":\"Fatemeh Gholizadeh,&nbsp;Gabriella Szalai,&nbsp;Tibor Janda\",\"doi\":\"10.1016/j.stress.2025.100879\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The 4-coumarate-CoA ligase (<em>4CL</em>) gene family plays a fundamental role in the phenylpropanoid pathway, influencing plant growth, lignin biosynthesis, and stress adaptation. Despite its significance, the <em>4CL</em> gene family in wheat (<em>T. aestivum</em> L.) has not been extensively studied. This study identified 40 <em>Ta4CL</em> genes distributed across 20 chromosomes, characterizing their structural features, phylogenetic relationships, and subcellular localization. Promoter analysis revealed cis-regulatory elements linked to stress response, hormone signaling, and light regulation. Gene expression analysis demonstrated that specific <em>Ta4CL</em> genes, such as <em>Ta4CL8–5A</em> and <em>Ta4CL4–7D</em>, were significantly upregulated under high salinity conditions, indicating their role in salt tolerance. Additionally, light-regulated cold acclimation experiments showed differential expression of multiple <em>Ta4CL</em> genes, with <em>Ta4CL2–6D</em> and <em>Ta4CL3–6B</em> displaying notable induction under blue light and cold stress. Protein interaction analysis highlighted the involvement of Ta4CLs in lignin and flavonoid biosynthesis, particularly through interactions with phenylalanine ammonia-lyase and other key enzymes in the phenylpropanoid pathway. Physiological assessments confirmed that Na<sup>+</sup> accumulation and the Na<sup>+</sup>/<em>K</em><sup>+</sup> ratio were correlated with the expression of specific <em>Ta4CL</em> genes, reinforcing their functional role in stress adaptation. These findings provide valuable insights into the diverse roles of <em>4CL</em> genes and offer potential targets for breeding stress-resilient wheat cultivars.</div></div>\",\"PeriodicalId\":34736,\"journal\":{\"name\":\"Plant Stress\",\"volume\":\"16 \",\"pages\":\"Article 100879\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-05-05\",\"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/S2667064X25001472\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X25001472","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

摘要

4-香豆酸辅酶a连接酶(4CL)基因家族在苯丙素途径中起着重要作用,影响植物生长、木质素生物合成和逆境适应。小麦4CL基因家族虽然具有重要意义,但尚未得到广泛的研究。本研究鉴定了分布在20条染色体上的40个Ta4CL基因,表征了它们的结构特征、系统发育关系和亚细胞定位。启动子分析揭示了与应激反应、激素信号转导和光调节相关的顺式调控元件。基因表达分析表明,Ta4CL特异性基因Ta4CL8-5A和Ta4CL4-7D在高盐条件下显著上调,表明其在耐盐性中起作用。此外,光调节冷驯化实验显示多个Ta4CL基因的差异表达,其中Ta4CL2-6D和Ta4CL3-6B在蓝光和冷胁迫下表现出显著的诱导作用。蛋白质相互作用分析强调了Ta4CLs参与木质素和类黄酮的生物合成,特别是通过与苯丙氨酸解氨酶和其他苯丙氨酸途径中的关键酶的相互作用。生理评估证实Na+积累和Na+/K+比值与特定Ta4CL基因的表达相关,强化了其在逆境适应中的功能作用。这些发现为了解4CL基因的不同作用提供了有价值的见解,并为培育抗胁迫小麦品种提供了潜在的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome-wide analysis of the 4-Coumarate-CoA ligase gene family in wheat: Expression patterns under salt stress and light-regulated cold acclimation
The 4-coumarate-CoA ligase (4CL) gene family plays a fundamental role in the phenylpropanoid pathway, influencing plant growth, lignin biosynthesis, and stress adaptation. Despite its significance, the 4CL gene family in wheat (T. aestivum L.) has not been extensively studied. This study identified 40 Ta4CL genes distributed across 20 chromosomes, characterizing their structural features, phylogenetic relationships, and subcellular localization. Promoter analysis revealed cis-regulatory elements linked to stress response, hormone signaling, and light regulation. Gene expression analysis demonstrated that specific Ta4CL genes, such as Ta4CL8–5A and Ta4CL4–7D, were significantly upregulated under high salinity conditions, indicating their role in salt tolerance. Additionally, light-regulated cold acclimation experiments showed differential expression of multiple Ta4CL genes, with Ta4CL2–6D and Ta4CL3–6B displaying notable induction under blue light and cold stress. Protein interaction analysis highlighted the involvement of Ta4CLs in lignin and flavonoid biosynthesis, particularly through interactions with phenylalanine ammonia-lyase and other key enzymes in the phenylpropanoid pathway. Physiological assessments confirmed that Na+ accumulation and the Na+/K+ ratio were correlated with the expression of specific Ta4CL genes, reinforcing their functional role in stress adaptation. These findings provide valuable insights into the diverse roles of 4CL genes and offer potential targets for breeding stress-resilient wheat cultivars.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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