Genome-wide identification and expression analysis of YTH gene family in barley reveals their potential role under abiotic stresses.

IF 2 4区 生物学 Q4 GENETICS & HEREDITY
Muhammad Mudasir, Muhammad Shahzad, Ayesha Bibi, Shareef Gul, Liu Qiuyi, Sarmad Frogh Arshad, Hameed Gul, Ali Shahzad
{"title":"Genome-wide identification and expression analysis of YTH gene family in barley reveals their potential role under abiotic stresses.","authors":"Muhammad Mudasir, Muhammad Shahzad, Ayesha Bibi, Shareef Gul, Liu Qiuyi, Sarmad Frogh Arshad, Hameed Gul, Ali Shahzad","doi":"10.1007/s10709-026-00260-z","DOIUrl":null,"url":null,"abstract":"<p><p>N6-methyladenosine (m<sup>6</sup>A) is a prevalent modification of eukaryotic mRNAs that plays a crucial role in gene regulation and genome integrity. YT521-B homology (YTH) domain-containing RNA-binding proteins act as essential m6A readers, influencing the fate of m<sup>6</sup>A-modified RNAs through their involvement in RNA splicing, processing, stability, and translation. In plants, YTH genes regulate plant growth and development by modulating these post-transcriptional processes. Despite the significance of barley (Hordeum vulgare L) as a staple crop, the YTH genes in this species remain largely unexplored. We conducted a detailed analysis of the barley genome and identified 14 YTH genes. Phylogenetic classification categorized these genes into 5 distinct groups. These genes are distributed across seven chromosomes, and their predicted protein products are primarily localized within the nucleus. We observed conserved exon structures and domains among the various groups of HvYTHs. Analysis of the promoter region identified several regulatory elements associated with developmental processes, stress responses, and hormone regulation. Protein-protein interaction predictions suggested associations with m<sup>6</sup>A methyltransferase components and stress-responsive factors. Additionally, miRNA target analysis identified potential post-transcriptional regulators of HvYTH genes. Expression profiling using RNA-seq data revealed both tissue-specific and stress-responsive patterns. Several HvYTH genes showing differential expression under cold, heat, and heavy metal stress. qRT-PCR validation confirmed the upregulation of HvYTH8 across all stress conditions, while HvYTH5, HvYTH10, and HvYTH12 members exhibited stress-specific upregulation or downregulation. These results underscore the functional divergence of HvYTH genes in mediating abiotic stress tolerance, providing potential targets for improving barley resilience.</p>","PeriodicalId":55121,"journal":{"name":"Genetica","volume":"154 1","pages":"11"},"PeriodicalIF":2.0000,"publicationDate":"2026-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetica","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10709-026-00260-z","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

N6-methyladenosine (m6A) is a prevalent modification of eukaryotic mRNAs that plays a crucial role in gene regulation and genome integrity. YT521-B homology (YTH) domain-containing RNA-binding proteins act as essential m6A readers, influencing the fate of m6A-modified RNAs through their involvement in RNA splicing, processing, stability, and translation. In plants, YTH genes regulate plant growth and development by modulating these post-transcriptional processes. Despite the significance of barley (Hordeum vulgare L) as a staple crop, the YTH genes in this species remain largely unexplored. We conducted a detailed analysis of the barley genome and identified 14 YTH genes. Phylogenetic classification categorized these genes into 5 distinct groups. These genes are distributed across seven chromosomes, and their predicted protein products are primarily localized within the nucleus. We observed conserved exon structures and domains among the various groups of HvYTHs. Analysis of the promoter region identified several regulatory elements associated with developmental processes, stress responses, and hormone regulation. Protein-protein interaction predictions suggested associations with m6A methyltransferase components and stress-responsive factors. Additionally, miRNA target analysis identified potential post-transcriptional regulators of HvYTH genes. Expression profiling using RNA-seq data revealed both tissue-specific and stress-responsive patterns. Several HvYTH genes showing differential expression under cold, heat, and heavy metal stress. qRT-PCR validation confirmed the upregulation of HvYTH8 across all stress conditions, while HvYTH5, HvYTH10, and HvYTH12 members exhibited stress-specific upregulation or downregulation. These results underscore the functional divergence of HvYTH genes in mediating abiotic stress tolerance, providing potential targets for improving barley resilience.

大麦YTH基因家族的全基因组鉴定和表达分析揭示了其在非生物胁迫下的潜在作用。
n6 -甲基腺苷(m6A)是一种常见的真核mrna修饰,在基因调控和基因组完整性中起着至关重要的作用。含有YT521-B同源性(YTH)结构域的RNA结合蛋白是必不可少的m6A读取器,通过参与RNA剪接、加工、稳定性和翻译,影响m6A修饰RNA的命运。在植物中,YTH基因通过调节这些转录后过程来调节植物的生长发育。尽管大麦(Hordeum vulgare L)作为一种主要作物具有重要意义,但该物种的YTH基因在很大程度上仍未被探索。我们对大麦基因组进行了详细的分析,鉴定出14个YTH基因。系统发育分类将这些基因分为5个不同的组。这些基因分布在7条染色体上,其预测的蛋白产物主要定位于细胞核内。我们观察到不同类群的HvYTHs外显子结构和结构域是保守的。对启动子区域的分析确定了与发育过程、应激反应和激素调节相关的几个调控元件。蛋白质相互作用预测表明与m6A甲基转移酶组分和应激反应因子有关。此外,miRNA靶分析确定了HvYTH基因潜在的转录后调节因子。使用RNA-seq数据的表达谱揭示了组织特异性和应激反应模式。几种HvYTH基因在冷、热和重金属胁迫下表现出差异表达。qRT-PCR验证证实HvYTH8在所有应激条件下均上调,而HvYTH5、HvYTH10和HvYTH12成员表现出应激特异性上调或下调。这些结果强调了HvYTH基因在介导非生物胁迫耐受方面的功能差异,为提高大麦抗逆性提供了潜在的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Genetica
Genetica 生物-遗传学
CiteScore
2.70
自引率
0.00%
发文量
32
审稿时长
>12 weeks
期刊介绍: Genetica publishes papers dealing with genetics, genomics, and evolution. Our journal covers novel advances in the fields of genomics, conservation genetics, genotype-phenotype interactions, evo-devo, population and quantitative genetics, and biodiversity. Genetica publishes original research articles addressing novel conceptual, experimental, and theoretical issues in these areas, whatever the taxon considered. Biomedical papers and papers on breeding animal and plant genetics are not within the scope of Genetica, unless framed in an evolutionary context. Recent advances in genetics, genomics and evolution are also published in thematic issues and synthesis papers published by experts in the field.
×
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