Article(id=1305139325029605577, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305139324555649224, articleNumber=null, orderNo=null, doi=10.7606/j.issn.1009-1041.2026.03.02, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1742572800000, receivedDateStr=2025-03-22, revisedDate=1746806400000, revisedDateStr=2025-05-10, acceptedDate=null, acceptedDateStr=null, onlineDate=1789099063402, onlineDateStr=2026-09-11, pubDate=1773504000000, pubDateStr=2026-03-15, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1789099063402, onlineIssueDateStr=2026-09-11, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1789099063402, creator=13701087609, updateTime=1789099063402, updator=13701087609, issue=Issue{id=1305139324555649224, tenantId=1146029695717560320, journalId=1303687221787852879, year='2026', volume='46', issue='3', pageStart='F2', pageEnd='424', issueExtLink='null', onlineDate='null', pubDate='1773504000000', pubDateStr='2026-03-15', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1789099063289, creator='13701087609', updateTime=1789103147683, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1305156455804465602, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305139324555649224, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1305156455804465603, tenantId=1146029695717560320, journalId=1303687221787852879, issueId=1305139324555649224, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=293, endPage=303, ext={EN=ArticleExt(id=1305139325222543562, articleId=1305139325029605577, tenantId=1146029695717560320, journalId=1303687221787852879, language=EN, title=Cloning and Analysis of the Cold Resistance Function of the TaIPT9A Gene in Winter Wheat(Triticum aestivum L.), columnId=1305133119129023428, journalTitle=Journal of Triticeae Crops, columnName=Genetics & Breeding, runingTitle=null, highlight=null, articleAbstract=

Cytokinins (CKs) play a pivotal regulatory role in plant growth, development and stress responses, with isopentenyltransferases (IPTs) serving as critical rate-limiting enzymes in CKs biosynthesis. To investigate the role of wheat IPT genes in plant responses to low-temperature stress, this study cloned the TaIPT9A gene (TraesCS7A02G560300) from the tiller nodes of the cold-resistant winter wheat cultivar Dongnong Dongmai 1(Dn1). Bioinformatics analysis, low-temperature-induced promoter activity assays, and functional characterization were conducted. The TaIPT9A gene was overexpressed in the cold-sensitive rice cultivar Longjing 11 via Agrobacterium-mediated transformation to preliminarily analyze its cold resistance function. The results showed that TaIPT9A has a coding sequence (CDS) of 1 362 bp, encoding 453 amino acids. Phylogenetic analysis revealed that wheat IPT proteins are most closely related to those of Aegilops tauschii. The TaIPT9A promoter contains cis-acting elements responsive to low temperature, light, ABA and MeJA, and its activity was induced by cold stress. Compared to wild-type rice, TaIPT9A-overexpressing plants exhibited greener leaves and better growth under low-temperature stress. Additionally, these plants showed significantly increased proline (Pro) content, catalase (CAT) activity, and upregulated expression of antioxidant enzyme-related genes (OsCATC, OsSOD1, OsSOD2 and OsAPX1) as well as cold resistance-related genes (OsCATC and OsDREB1A). These findings suggest that TaIPT9A enhances cold tolerance in rice seedlings.

, authors=Huishan SONG, Chen SUN, Yayun LIU, Qingchuan SUN, Da ZHANG, authorsList=Huishan SONG, Chen SUN, Yayun LIU, Qingchuan SUN, Da ZHANG, authorCompany=null, correspAuthors=Da ZHANG, 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=1305139325440647371, articleId=1305139325029605577, tenantId=1146029695717560320, journalId=1303687221787852879, language=CN, title=冬小麦TaIPT9A基因的克隆及抗寒功能分析, columnId=1305133119284212678, journalTitle=麦类作物学报, columnName=遗传育种, runingTitle=null, highlight=null, articleAbstract=

细胞分裂素（CKs）在植物生长发育和逆境应答中发挥重要的调控作用，异戊烯基转移酶（IPTs）是CKs生物合成的重要限速酶。为了探究小麦IPT编码基因在植物低温胁迫应答中的作用，从强抗寒冬小麦品种东农冬麦1号（Dn1）分蘖节中克隆了TaIPT9A基因（TraesCS7A02G560300），对其进行生物信息学分析、低温下启动子活性分析，并采用农杆菌介导法将其转入水稻冷敏感品种龙粳11中，对创建的含有TaIPT9A的株系的抗寒功能进行初步分析。结果表明，TaIPT9A基因的CDS为1 362 bp，编码453个氨基酸；小麦与粗山羊草IPT蛋白亲缘关系最近；TaIPT9A启动子区含有响应低温、光、ABA、MeJA等顺式作用元件，TaIPT9A启动子活性受低温诱导。与野生型相比，过表达TaIPT9A基因水稻的叶片在低温胁迫下更翠绿、生长状态更好；叶片的脯氨酸（Pro）含量、过氧化氢酶（CAT）活性、抗氧化酶相关基因（OsCATC、OsSOD1、OsSOD2和OsAPX1）及抗寒相关基因（OsCATC、OsDREB1A）的表达量显著提高。这说明TaIPT9A基因增强了水稻幼苗的抗寒性。

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E-mail: 3335761856@qq.com（宋慧珊）

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E-mail: 3335761856@qq.com（宋慧珊）

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