Genome-wide identification of the MYB transcription factor family in kiwifruit and analysis of its expression pattern in response to salt stress

IF 2.2 4区 生物学 Q2 PLANT SCIENCES
Chaoying Chen, Wenjuan Zhao, Xulin Li, Ke Wen, Yinqiang Zi, Ke Zhao, Daming Chen, Hanyao Zhang, Xiaozhen Liu
{"title":"Genome-wide identification of the MYB transcription factor family in kiwifruit and analysis of its expression pattern in response to salt stress","authors":"Chaoying Chen,&nbsp;Wenjuan Zhao,&nbsp;Xulin Li,&nbsp;Ke Wen,&nbsp;Yinqiang Zi,&nbsp;Ke Zhao,&nbsp;Daming Chen,&nbsp;Hanyao Zhang,&nbsp;Xiaozhen Liu","doi":"10.1007/s11738-025-03819-z","DOIUrl":null,"url":null,"abstract":"<div><p>As the king of vitamin C, kiwifruit has high nutritional and economic value. However, with the expansion of its planting area and the application of a large amount of farm manure represented by large livestock manure, kiwifruit is at increasing risk of salt stress, so it is urgent to select salt-tolerant strains of kiwifruit. MYB transcription factors (TFs) play a vital role in responding to abiotic stress and regulating the synthesis of secondary metabolites. There are relatively few reports on the specific gene functions of MYB TFs. In this study, based on the kiwifruit genome database and transcriptome sequencing data, we used bioinformatics to analyze the structure, evolution, and expression patterns of kiwifruit MYB TFs. The results showed that 226 AcMYB TFs were identified, and the phylogenetic analysis classified them into 32 subfamilies. Analysis of the gene structure and conserved motifs revealed that the exon and intron structures of <i>AcMYB</i> in the same subfamily are relatively identical, with only minor differences. In addition, we predicted cis-acting elements associated with hormones, light responses, etc., at the 2000 bp upstream position of the promoter of the AcMYB TFs. Expression profiling based on transcriptome data showed a total of 24 differentially significant genes, of which 11 genes were upregulated, and 13 genes were downregulated. <i>AcMYB100</i>, <i>AcMYB186</i>, <i>AcMYB81</i>, and so on upregulated genes by positively regulating salt stress to minimize the effects caused to the plants, <i>AcMYB145</i>, <i>AcMYB88</i>, <i>AcMYB1</i>, and so on downregulated genes reduced the salt stress effects on plants by negatively regulating salt stress. It suggests that these MYB TFs can modify the effects of salt on kiwifruit. We also identified the signaling pathway of stress regulating MYB TFs in response to salt stress in kiwifruit plants. These results provide a basis for understanding the biological functions and characteristics of the MYB TF family and lay a foundation for further research on salt tolerance breeding in kiwifruit.</p></div>","PeriodicalId":6973,"journal":{"name":"Acta Physiologiae Plantarum","volume":"47 7","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Physiologiae Plantarum","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s11738-025-03819-z","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

As the king of vitamin C, kiwifruit has high nutritional and economic value. However, with the expansion of its planting area and the application of a large amount of farm manure represented by large livestock manure, kiwifruit is at increasing risk of salt stress, so it is urgent to select salt-tolerant strains of kiwifruit. MYB transcription factors (TFs) play a vital role in responding to abiotic stress and regulating the synthesis of secondary metabolites. There are relatively few reports on the specific gene functions of MYB TFs. In this study, based on the kiwifruit genome database and transcriptome sequencing data, we used bioinformatics to analyze the structure, evolution, and expression patterns of kiwifruit MYB TFs. The results showed that 226 AcMYB TFs were identified, and the phylogenetic analysis classified them into 32 subfamilies. Analysis of the gene structure and conserved motifs revealed that the exon and intron structures of AcMYB in the same subfamily are relatively identical, with only minor differences. In addition, we predicted cis-acting elements associated with hormones, light responses, etc., at the 2000 bp upstream position of the promoter of the AcMYB TFs. Expression profiling based on transcriptome data showed a total of 24 differentially significant genes, of which 11 genes were upregulated, and 13 genes were downregulated. AcMYB100, AcMYB186, AcMYB81, and so on upregulated genes by positively regulating salt stress to minimize the effects caused to the plants, AcMYB145, AcMYB88, AcMYB1, and so on downregulated genes reduced the salt stress effects on plants by negatively regulating salt stress. It suggests that these MYB TFs can modify the effects of salt on kiwifruit. We also identified the signaling pathway of stress regulating MYB TFs in response to salt stress in kiwifruit plants. These results provide a basis for understanding the biological functions and characteristics of the MYB TF family and lay a foundation for further research on salt tolerance breeding in kiwifruit.

猕猴桃MYB转录因子家族的全基因组鉴定及其对盐胁迫的表达模式分析
猕猴桃作为维生素C之王,具有很高的营养价值和经济价值。然而,随着猕猴桃种植面积的扩大和以大量畜禽粪便为代表的大量农畜粪便的施用,猕猴桃遭受盐胁迫的风险越来越大,因此选择耐盐猕猴桃品系迫在眉睫。MYB转录因子(TFs)在应对非生物胁迫和调节次生代谢产物合成中起着至关重要的作用。关于MYB tf的特定基因功能的报道相对较少。本研究基于猕猴桃基因组数据库和转录组测序数据,利用生物信息学方法分析了猕猴桃MYB tf的结构、进化和表达模式。结果发现226个AcMYB TFs,系统发育分析将其划分为32个亚家族。对基因结构和保守基序的分析表明,同一亚家族AcMYB的外显子和内含子结构相对相同,只有微小的差异。此外,我们在AcMYB TFs启动子上游2000 bp的位置预测了与激素、光响应等相关的顺式作用元件。基于转录组数据的表达谱分析显示,共有24个差异显著基因,其中11个基因表达上调,13个基因表达下调。AcMYB100、AcMYB186、AcMYB81等上调基因通过正向调控盐胁迫来降低对植物的影响,AcMYB145、AcMYB88、AcMYB1等下调基因通过负向调控盐胁迫来降低盐胁迫对植物的影响。这表明这些MYB TFs可以改变盐对猕猴桃的影响。我们还发现了胁迫调节MYB TFs在猕猴桃植物中响应盐胁迫的信号通路。这些结果为了解MYB TF家族的生物学功能和特性提供了基础,并为进一步研究猕猴桃耐盐育种奠定了基础。
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
Acta Physiologiae Plantarum
Acta Physiologiae Plantarum 生物-植物科学
CiteScore
5.10
自引率
3.80%
发文量
125
审稿时长
3.1 months
期刊介绍: Acta Physiologiae Plantarum is an international journal established in 1978 that publishes peer-reviewed articles on all aspects of plant physiology. The coverage ranges across this research field at various levels of biological organization, from relevant aspects in molecular and cell biology to biochemistry. The coverage is global in scope, offering articles of interest from experts around the world. The range of topics includes measuring effects of environmental pollution on crop species; analysis of genomic organization; effects of drought and climatic conditions on plants; studies of photosynthesis in ornamental plants, and more.
×
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