Article(id=1277253952613778349, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277253949203809194, articleNumber=null, orderNo=null, doi=10.3969/j.issn.1000-2561.2026.01.015, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1757606400000, receivedDateStr=2025-09-12, revisedDate=null, revisedDateStr=null, acceptedDate=1760716800000, acceptedDateStr=2025-10-18, onlineDate=1782450672533, onlineDateStr=2026-06-26, pubDate=1769270400000, pubDateStr=2026-01-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782450672533, onlineIssueDateStr=2026-06-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782450672533, creator=13701087609, updateTime=1782450672533, updator=13701087609, issue=Issue{id=1277253949203809194, tenantId=1146029695717560320, journalId=1235980609244409860, year='2026', volume='47', issue='1', pageStart='1', pageEnd='280', issueExtLink='null', onlineDate='null', pubDate='1769270400000', pubDateStr='2026-01-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1782450671721, creator='13701087609', updateTime=1782451647086, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1277258041263256431, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277253949203809194, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1277258041263256432, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1277253949203809194, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=154, endPage=164, ext={EN=ArticleExt(id=1277253953481999279, articleId=1277253952613778349, tenantId=1146029695717560320, journalId=1235980609244409860, language=EN, title=Isolation of the MiPIN1 Promoter and Screening of Its Upstream Regulators in Mango, columnId=1236256430337085821, journalTitle=Chinese Journal of Tropical Crops, columnName=Omics & Biotechnology, runingTitle=null, highlight=null, articleAbstract=

The induction of adventitious roots (AR) is a key step for successful clonal propagation in plants. Previous studies have shown that the auxin polar transport carrier MiPIN1 plays an important role in AR formation from mango cotyledon segments, yet its upstream regulatory mechanisms remain unclear. In this study, a 2 112 bp promoter sequence of MiPIN1 isolated using FPNI-PCR. Bioinformatic analysis revealed that the promoter region contained various cis-acting elements, including those involved in light response, MYB binding, abscisic acid response, and low-temperature stress. A bait vector, pAbAi-MiPIN1, was constructed, and the minimal concentration of Aureobasidin A (AbA) required to suppress autoactivation in the yeast system was determined to be 500 ng/mL. Furthermore, a yeast cDNA library was constructed from mango cotyledon segments during AR formation. Using the yeast one-hybrid (Y1H) system, 62 upstream proteins that potentially bind to the MiPIN1 promoter were identified, including auxin-binding protein ABP19a-like, zinc finger protein CCCH, MYB308, 8-hydroxygeraniol dehydrogenase, and chlorophyll a-b binding protein LHCII. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses indicated that the proteins were mainly involved in biological processes such as cellular processes, metabolism, response to stimuli, and biological regulation. They were also enriched in metabolic pathways related to secondary metabolite biosynthesis, energy metabolism, and the metabolism of amino acids, lipids, and carbohydrates. The findings would lay a foundation for unraveling the molecular regulatory network underlying adventitious root formation in mango.

, authors=null, authorsList=Yuxing WEN, Yanying WANG, Binbin CAI, Chengying ZENG, Yunhe LI, authorCompany=null, correspAuthors=Yunhe LI, 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=1277253955214246833, articleId=1277253952613778349, tenantId=1146029695717560320, journalId=1235980609244409860, language=CN, title=杧果MiPIN1启动子克隆及上游调控因子筛选, columnId=1236256430517440904, journalTitle=热带作物学报, columnName=组学与生物技术, runingTitle=null, highlight=null, articleAbstract=

不定根的诱导是植物无性繁殖成功的关键环节。前期研究表明，生长素极性运输载体基因MiPIN1在杧果子叶切段不定根形成中起着重要作用，但其上游调控机制尚不明确。本研究首先通过FPNI-PCR法分离到一段长度为2112 bp的MiPIN1基因启动子序列，该启动子区域包含光反应、MYB结合、脱落酸反应、低温响应等多种顺式作用元件。随后构建pAbAi-MiPIN1诱饵载体，并确定其在酵母系统中的自激活抑制浓度为500 ng/mL AbA。进一步构建杧果子叶切段不定根形成的酵母cDNA文库，并利用酵母单杂交系统筛选到62个与MiPIN1启动子结合的上游候选蛋白，包括生长素结合蛋白ABP19a-like、锌指蛋白CCCH、myb 308蛋白、8-羟基香叶醇脱氢酶、叶绿素结合蛋白LCHII等。GO和KEGG富集分析显示，这些蛋白主要参与细胞进程、代谢过程、刺激响应、生物调节等生物过程，并涉及次生代谢物的生物合成、能量代谢、氨基酸代谢、脂类代谢和碳水化合物等新陈代谢途径。本研究为系统解析杧果不定根形成的分子调控网络奠定基础。

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温雨兴（2000—），女，硕士研究生，研究方向：植物分子生物学。

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温雨兴（2000—），女，硕士研究生，研究方向：植物分子生物学。

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