Article(id=1305133123558204047, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305133116104925797, articleNumber=null, orderNo=null, doi=10.7606/j.issn.1009-1041.2026.08.02, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1761148800000, receivedDateStr=2025-10-23, revisedDate=1763395200000, revisedDateStr=2025-11-18, acceptedDate=null, acceptedDateStr=null, onlineDate=1789097584857, onlineDateStr=2026-09-11, pubDate=1786723200000, pubDateStr=2026-08-15, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1789097584857, onlineIssueDateStr=2026-09-11, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1789097584857, creator=13701087609, updateTime=1789097584857, updator=13701087609, issue=Issue{id=1305133116104925797, tenantId=1146029695717560320, journalId=1303687221787852879, year='2026', volume='46', issue='8', pageStart='F2', pageEnd='1130', issueExtLink='null', onlineDate='null', pubDate='1786723200000', pubDateStr='2026-08-15', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1789097583080, creator='13701087609', updateTime=1789103064032, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1305156104980296075, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305133116104925797, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1305156104980296076, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305133116104925797, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1000, endPage=1013, ext={EN=ArticleExt(id=1305133123751142033, articleId=1305133123558204047, tenantId=1146029695717560320, journalId=1303687221787852879, language=EN, title=Identification of the R2R3-MYB Transcription Factor Family in Barley and Functional Verification of Hv2RMYB-48 under Low-Phosphorus Stress, columnId=1305133119129023428, journalTitle=Journal of Triticeae Crops, columnName=Genetics & Breeding, runingTitle=null, highlight=null, articleAbstract=

The R2R3-MYB transcription factor family, the largest subfamily of MYB transcription factors, plays critical roles in various plant stress responses. However, its function under low-phosphate (P) stress remains poorly characterized. In this study, a total of 127 R2R3-MYB genes were identified in the barley MorexV3 genome using bioinformatic approaches and designated as Hv2RMYB-1 to Hv2RMYB-127. These genes were predominantly distributed on the 7 barley chromosomes and were found to harbor hormone-responsive cis-acting elements in their promoter regions. Physicochemical analysis revealed that most members encode acidic and unstable proteins. Phylogenetic and collinearity analyses classified the barley R2R3-MYB family into five distinct clades, including 16 pairs of tandemly duplicated genes. Based on transcriptomic data (RNA-Seq) and quantitative real-time PCR (qRT-PCR), 10 barley R2R3-MYB genes showed differential expression under low-Phosphorus stress, among which Hv2RMYB-48 was notably upregulated. Further investigation confirmed that Hv2RMYB-48 localizes to the nucleus and can bind to the MYB-ABRE-MYBcis-element.

, authors=Changjie Wang^{1, 2}, Xinyao Wang^{1, 2}, Jiajia Chen^{1, 2}, Na Zhao^{1, 2}, Yongsheng Wang^{1, 2}, Li Niu^{1, 2}, Hong Zhang^{1, 2}, Lirong Yao^{1, 2}, Erjing Si^{1, 2}, Ke Yang^{1, 2}, Yaxiong Meng^{1, 2}, Xiaole Ma^{1, 2}, Huajun Wang^{1, 2}, Juncheng Wang^{1, 2}, authorsList=Changjie Wang, Xinyao Wang, Jiajia Chen, Na Zhao, Yongsheng Wang, Li Niu, Hong Zhang, Lirong Yao, Erjing Si, Ke Yang, Yaxiong Meng, Xiaole Ma, Huajun Wang, Juncheng Wang, authorCompany=null, correspAuthors=Huajun Wang, Juncheng Wang, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1305133124166378130, articleId=1305133123558204047, tenantId=1146029695717560320, journalId=1303687221787852879, language=CN, title=大麦R2R3-MYB转录因子家族鉴定及低磷胁迫下Hv2RMYB-48的功能验证, columnId=1305133119284212678, journalTitle=麦类作物学报, columnName=遗传育种, runingTitle=null, highlight=null, articleAbstract=

R2R3-MYB转录因子家族是MYB转录因子中最大亚家族，在植物多种胁迫响应中扮演重要角色。为了筛选出与磷利用效率相关的R2R3-MYB成员，以最新组装的大麦MorexV3基因组对大麦中的R2R3-MYB转录因子家族进行了鉴定与生物信息学分析。结果表明，在大麦MorexV3基因组中鉴定出127个R2R3-MYB基因，并命名为Hv2RMYB-1~Hv2RMYB-127。这些基因分布于大麦7条染色体上，且启动子区富含激素响应顺式作用元件。经理化性质分析，大多数成员编码酸性且不稳定的蛋白质。通过系统发育及共线性分析将大麦R2R3-MYB家族划分为5个不同的分支及16对串联复制基因。结合转录组数据（RNA-Seq）和实时荧光定量PCR技术（qRT-PCR），发现10个大麦R2R3-MYB基因在低磷胁迫下均有不同程度的差异性表达，其中Hv2RMYB-48显著上调表达。Hv2RMYB-48定位于细胞核，可以与MYB-ABRE-MYB顺式作用元件进行互作。

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