Article(id=1276531539429158920, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276531538535781212, articleNumber=null, orderNo=null, doi=10.3969/j.issn.1000-2561.2025.04.004, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1732809600000, receivedDateStr=2024-11-29, revisedDate=null, revisedDateStr=null, acceptedDate=1734537600000, acceptedDateStr=2024-12-19, onlineDate=1782278435808, onlineDateStr=2026-06-24, pubDate=1745510400000, pubDateStr=2025-04-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782278435808, onlineIssueDateStr=2026-06-24, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782278435808, creator=13701087609, updateTime=1782278435808, updator=13701087609, issue=Issue{id=1276531538535781212, tenantId=1146029695717560320, journalId=1235980609244409860, year='2025', volume='46', issue='4', pageStart='777', pageEnd='1024', issueExtLink='null', onlineDate='null', pubDate='1745510400000', pubDateStr='2025-04-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1782278435595, creator='13701087609', updateTime=1782278607615, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1276532260098675208, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276531538535781212, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1276532260098675209, tenantId=1146029695717560320, journalId=1235980609244409860, issueId=1276531538535781212, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=807, endPage=819, ext={EN=ArticleExt(id=1276531539668234250, articleId=1276531539429158920, tenantId=1146029695717560320, journalId=1235980609244409860, language=EN, title=Genome-wide Identification of HSF Gene Family and Their Response to Hot Ambient Temperature During Flower Development in Passion Fruit (Passiflora edulis), columnId=1236256430337085821, journalTitle=Chinese Journal of Tropical Crops, columnName=Omics & Biotechnology, runingTitle=null, highlight=null, articleAbstract=

Heat shock transcription factor (HSF) is an important regulatory factor that plays a crucial role in plant response to hot ambient temperature (HAT). High temperature stress has a serious negative impact on the flowering of passion fruit, therefore, studying the regulation of heat tolerance by HSF in passion fruit is of great significance. In this study, we identified 26 HSF genes on the genome of passion fruit using bioinformatics technology, named PeHSF1-PeHSF26. The genes could encode proteins of 100-1589 amino acids, with molecular weight 11 544.9-177 157.8 g/mol, and a theoretical isoelectric point of 4.25-10.80. The 26 genes were distributed on chromosomes 1, 4, 5, 6, 7, 8 and 9, and were divided into 10 subpopulations. The analysis of the whole genome replication event showed that ZX01G0033270, ZX01G0052790 and ZX01G0052980 were located within the genome duplications. The genes contained 1-12 introns and 2-13 exons, all contained HSF-DNA binding domains. RNA-seq analysis of Huangguo original species and Jinlingziguo HSF genes to HAT revealed that there were significant differences in the expression levels of genes, including ZX01G0002530, ZX01G0052790 and ZX01G0121040 in flower buds. The expression levels of candidate HSF genes were validated by RT-qPCR. Based on comprehensive analysis, it is supposed that the most ideal candidate HSF gene for passion flower response to high temperature stress was ZX01G0121040. The results would contribute to understand the function of HSF in response to high temperature stress during the flowering of passion fruit, and provide important genetic resources and theoretical basis for genetic improvement of passion fruit.

, authors=null, authorsList=Yanyan WU, Jieyun LIU, Junniu ZHOU, Qinglan TIAN, Weihua HUANG, Chenli ZHU, Haifei MOU, authorCompany=null, correspAuthors=Yanyan WU, Haifei MOU, 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=1276531543547965472, articleId=1276531539429158920, tenantId=1146029695717560320, journalId=1235980609244409860, language=CN, title=西番莲HSF基因家族的全基因组鉴定及成花期对高温胁迫的响应, columnId=1236256430517440904, journalTitle=热带作物学报, columnName=组学与生物技术, runingTitle=null, highlight=null, articleAbstract=

热激转录因子(heat shock transcription factor,HSF)是重要的调节因子,在植物响应高温胁迫中发挥重要作用。高温胁迫对西番莲成花造成了严重的负面影响,因此研究HSF调控西番莲耐热性的意义重大。本研究利用生物信息学技术在西番莲基因组上鉴定了26个热激转录因子基因,分别命名为PeHSF1~PeHSF26。西番莲HSF基因编码蛋白长度为100~1589个氨基酸,分子量为11 544.9~177 157.8 g/mol,理论等电点为4.25~10.80。西番莲26个HSF基因分布在第1、4、5、6、7、8和9染色体上,分为10个亚群。西番莲全基因组复制事件分析结果表明,ZX01G0033270ZX01G0052790ZX01G0052980等5个HSF基因位于重复片段内。西番莲HSF基因有1~12个内含子和2~13个外显子,都包含HSF-DNA结合结构域。利用RNA-seq分析黄果原生种与金陵紫果HSF基因对高温环境的响应,发现ZX01G0002530ZX01G0052790ZX01G0121040等基因在花蕾中表达量差异显著,并通过RT-qPCR验证候选HSF基因表达水平。综合分析,推测西番莲响应高温胁迫的最理想的候选HSF基因为ZX01G0121040。这些结果有助于了解HSF在西番莲成花期响应高温胁迫过程中的功能,为西番莲耐高温的遗传改良提供重要基因资源和理论依据。

, authors=

吴艳艳(1984—),女,硕士,副研究员,研究方向:西番莲等特色果树种质资源收集与创新利用。

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* 牟海飞(MOU Haifei),E-mail:
吴艳艳(WU Yanyan),E-mail:
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吴艳艳(1984—),女,硕士,副研究员,研究方向:西番莲等特色果树种质资源收集与创新利用。

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吴艳艳(1984—),女,硕士,副研究员,研究方向:西番莲等特色果树种质资源收集与创新利用。

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(in Chinese), articleTitle=Research progress of PPR protein in plant abiotic stress response, refAbstract=null), Reference(id=1276531562783043735, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, doi=null, pmid=null, pmcid=null, year=2019, volume=27, issue=2, pageStart=225, pageEnd=234, url=null, language=null, rfNumber=[28], rfOrder=29, authorNames=王婉珍, 任育军, 缪颖, journalName=热带亚热带植物学报, refType=null, unstructuredReference=王婉珍, 任育军, 缪颖. 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(in Chinese), articleTitle=Roles of PPR proteins in plant growth and development, refAbstract=null), Reference(id=1276531562917261465, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, doi=null, pmid=null, pmcid=null, year=2003, volume=54, issue=384, pageStart=1069, pageEnd=1074, url=null, language=null, rfNumber=[29], rfOrder=31, authorNames=KUZUYA M, HOSOYA K, YASHIRO K, TOMITA K, EZURA H, journalName=Journal of Experimental Botany, refType=null, unstructuredReference=KUZUYA M, HOSOYA K, YASHIRO K, TOMITA K, EZURA H. Powdery mildew (Sphaerotheca fuliginea) resistance in melon is selectable at the haploid level[J]. 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Plant and Cell Physiology, 2009, 50(12): 2023-2033., articleTitle=Dynamic aspects of ion accumulation by vesicle traffic under salt stress in Arabidopsis, refAbstract=null), Reference(id=1276531563076645019, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, doi=null, pmid=null, pmcid=null, year=2021, volume=108, issue=1, pageStart=169, pageEnd=182, url=null, language=null, rfNumber=[31], rfOrder=33, authorNames=WEI Y, JIN J T, XU Y X, LIU W T, YANG G X, BU H D, LI T, WANG A D, journalName=The Plant Journal, refType=null, unstructuredReference=WEI Y, JIN J T, XU Y X, LIU W T, YANG G X, BU H D, LI T, WANG A D. Ethylene-activated MdPUB24 mediates ubiquitination of MdBEL7 to promote chlorophyll degradation in apple fruit[J]. The Plant Journal, 2021, 108(1): 169-182., articleTitle=Ethylene-activated MdPUB24 mediates ubiquitination of MdBEL7 to promote chlorophyll degradation in apple fruit, refAbstract=null)], funds=[Fund(id=1276531558538408056, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, awardId=32260740; 32060660, language=CN, fundingSource=国家自然科学基金项目(32260740; 32060660), fundOrder=null, country=null), Fund(id=1276531558630682745, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, awardId=2023GXNSFAA026301, language=CN, fundingSource=广西自然科学基金项目(2023GXNSFAA026301), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1276531543799623714, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, xref=1., ext=[AuthorCompanyExt(id=1276531543808012323, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, companyId=1276531543799623714, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.Biotechnology Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi 530007, China), AuthorCompanyExt(id=1276531543816400932, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, companyId=1276531543799623714, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.广西壮族自治区农业科学院生物技术研究所,广西南宁 530007)]), AuthorCompany(id=1276531543900287013, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, xref=2., ext=[AuthorCompanyExt(id=1276531543917064230, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, companyId=1276531543900287013, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.Guangxi Academy of Agricultural Sciences, Nanning, Guangxi 530007, China), AuthorCompanyExt(id=1276531543929647143, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, companyId=1276531543900287013, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.广西壮族自治区农业科学院,广西南宁 530007)])], figs=[ArticleFig(id=1276531554369269852, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 1, caption=Structure of mature nodes in passion fruit, figureFileSmall=A+VgHwzouUtPC0Q7Tnl6nA==, figureFileBig=hwk9oTVls9+0yqQs7agctw==, tableContent=null), ArticleFig(id=1276531554738368605, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图1, caption=西番莲成熟节点的结构

F:花蕾;T:卷须;L:叶片;S:茎秆。

, figureFileSmall=A+VgHwzouUtPC0Q7Tnl6nA==, figureFileBig=hwk9oTVls9+0yqQs7agctw==, tableContent=null), ArticleFig(id=1276531556487393374, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 2, caption=Phylogenetic tree of HSF in passion fruit and six species, figureFileSmall=RTk+OJEgxYaw1loEjJFCRw==, figureFileBig=8HIqB8TCDa8e4Nv1Cbxo1Q==, tableContent=null), ArticleFig(id=1276531556600639583, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图2, caption=西番莲与6个物种的HSF系统进化树

A:西番莲HSF系统进化树;B:西番莲、拟南芥、水稻、番茄、单瓣茉莉花、木薯和玉米的HSF系统进化树。

, figureFileSmall=RTk+OJEgxYaw1loEjJFCRw==, figureFileBig=8HIqB8TCDa8e4Nv1Cbxo1Q==, tableContent=null), ArticleFig(id=1276531556676137056, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 3, caption=Collinearity of HSF gene in passion fruit, figureFileSmall=TBXFkl/Xv90Prcwpi9NZ1g==, figureFileBig=3Md9GtEjBfu9qBZWgQJT7Q==, tableContent=null), ArticleFig(id=1276531556772606049, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图3, caption=西番莲HSF基因的共线性

橙色线条表示HSF基因共线性区域

, figureFileSmall=TBXFkl/Xv90Prcwpi9NZ1g==, figureFileBig=3Md9GtEjBfu9qBZWgQJT7Q==, tableContent=null), ArticleFig(id=1276531556848103522, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 4, caption=WGD events and Ks density of passion fruit, figureFileSmall=Y2IvsDtgKjnjSX5WHmW25Q==, figureFileBig=pgddUH25kBe5gXA9IT7zrA==, tableContent=null), ArticleFig(id=1276531556919406691, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图4, caption=西番莲WGD事件和Ks密度图, figureFileSmall=Y2IvsDtgKjnjSX5WHmW25Q==, figureFileBig=pgddUH25kBe5gXA9IT7zrA==, tableContent=null), ArticleFig(id=1276531556978126948, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 5, caption=Gene structure and clustering of HSF in passion fruit, figureFileSmall=oyPSojsZEyeMtIPkhQbnUQ==, figureFileBig=c+yqRo8CT4PIDSZD4PJBoQ==, tableContent=null), ArticleFig(id=1276531557045235813, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图5, caption=西番莲HSF基因结构及聚类, figureFileSmall=oyPSojsZEyeMtIPkhQbnUQ==, figureFileBig=c+yqRo8CT4PIDSZD4PJBoQ==, tableContent=null), ArticleFig(id=1276531557137510502, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 6, caption=Effect of flower development in passion fruit under hot ambient temperature, figureFileSmall=0P5QZHevFdgn6bYIZXTQKQ==, figureFileBig=oMM+o/XyNABld9ScKUilbA==, tableContent=null), ArticleFig(id=1276531557204619367, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图6, caption=高温环境对西番莲金陵紫果和黄果原生种成花的影响

A:金陵紫果(ZG),花蕾正常;B:黄果原生种(HG),花蕾败育;C:紫果与黄果原生种花蕾的比较。标尺=1 cm。

, figureFileSmall=0P5QZHevFdgn6bYIZXTQKQ==, figureFileBig=oMM+o/XyNABld9ScKUilbA==, tableContent=null), ArticleFig(id=1276531557292699752, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 7, caption=Principal component analysis of 24 samples during flowering of passion fruit, figureFileSmall=AZSks9nb6qOKEnlA7l4RUg==, figureFileBig=QQ2fFG4oHBwhZs6X9hbj3g==, tableContent=null), ArticleFig(id=1276531557368197225, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图7, caption=西番莲成花期24个样品的主成分分析

A1:HG花蕾,A2:ZG花蕾;B1:HG卷须,B2:ZG卷须;C1:HG茎,C2:ZG茎;D1:HG叶片,D2:ZG叶片。

, figureFileSmall=AZSks9nb6qOKEnlA7l4RUg==, figureFileBig=QQ2fFG4oHBwhZs6X9hbj3g==, tableContent=null), ArticleFig(id=1276531557452083306, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 8, caption=DEGs of 24 samples during flowering of passion fruit, figureFileSmall=+lHj7H1aYnujInSEU6ScZQ==, figureFileBig=enTKRx5E6RQGjAGW6sVm+Q==, tableContent=null), ArticleFig(id=1276531557527580779, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图8, caption=西番莲成花期24个样品的基因表达量差异

A1:HG花蕾,A2:ZG花蕾;B1:HG卷须,B2:ZG卷须;C1:HG茎,C2:ZG茎;D1:HG叶片,D2:ZG叶片。

, figureFileSmall=+lHj7H1aYnujInSEU6ScZQ==, figureFileBig=enTKRx5E6RQGjAGW6sVm+Q==, tableContent=null), ArticleFig(id=1276531557590495340, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 9, caption=Expression patterns and clustering of HSF genes in passion fruit, figureFileSmall=ikH+0tNRUwBWu7cEfDD9qg==, figureFileBig=qAxl9dQFR8NDvJfcNFMXkA==, tableContent=null), ArticleFig(id=1276531557657604205, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图9, caption=西番莲HSF基因表达模式及聚类, figureFileSmall=ikH+0tNRUwBWu7cEfDD9qg==, figureFileBig=qAxl9dQFR8NDvJfcNFMXkA==, tableContent=null), ArticleFig(id=1276531557724713070, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Fig. 10, caption=Relative expression of 10 HSF genes in Jinlingziguo and Huangguoyuanshengzhong flower bud using RT-qPCR, figureFileSmall=JWT3w7RjcJj/WVB/rrz/9w==, figureFileBig=PP6/59iDBQ9a0OnBpmfgxA==, tableContent=null), ArticleFig(id=1276531557791821935, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=图10, caption=利用RT-qPCR检测10个HSF基因在金陵紫果和黄果原生种花蕾的表达水平

**表示差异极显著(P<0.01),***表示差异极显著(P<0.0001)。

, figureFileSmall=JWT3w7RjcJj/WVB/rrz/9w==, figureFileBig=PP6/59iDBQ9a0OnBpmfgxA==, tableContent=null), ArticleFig(id=1276531557867319408, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Tab. 1, caption=

Information of gene and primers using for RT-qPCR

, figureFileSmall=null, figureFileBig=null, tableContent=
基因名称Gene name正向引物序列(5′–3′)Forward primer sequence (5′–3′)反向引物序列(5′–3′)Reverse primer sequence (5′–3′)产物大小Product size/bp
EF1GGCTGAGCGTGAACGTGGTACGGCACAATCAGCCTGGGAA146
ZX01G0002530TGGAACCTCTTCTTCGCAGTCCGTTGTCCTTCTTCAGCCTCT146
ZX01G0052790AAGCGGAGATAGGAACGAACATAGCAGCAGAGAAGAGAAGAAGG122
ZX01G0121040ATCAGTGCGATGCGTCAGTTGTCGTAAGTCTTGCTCAGGAA114
ZX04G0012630TCCAACACCAACAGCAACACGTATTCAACTGCCTAACGAAGC188
ZX05G0014510GAACTCAAGAATCCATAGCAAGCATGAAGAGGAGAAGAGCAGTCAAGAA150
ZX06G0002180TTGGCAGTGATAGTTGTTGGTTGAGTCCGTGGAAGCATCGT156
ZX06G0012300TTAGTGGAAGAAGGTGAAGGTGAAGAAGTTGTTGTGCTTGAAGTATCTG147
ZX07G0010660CGCAGGAACTCATCGGTCAATGGTGTTGGCATGGATCTCTG179
ZX08G0002060CATTGCGTTGAAGTTGGAAGGTCCTCGTCATCTGCTGTTGCT183
), ArticleFig(id=1276531557942816881, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=表1, caption=

RT-qPCR相关基因及引物信息

, figureFileSmall=null, figureFileBig=null, tableContent=
基因名称Gene name正向引物序列(5′–3′)Forward primer sequence (5′–3′)反向引物序列(5′–3′)Reverse primer sequence (5′–3′)产物大小Product size/bp
EF1GGCTGAGCGTGAACGTGGTACGGCACAATCAGCCTGGGAA146
ZX01G0002530TGGAACCTCTTCTTCGCAGTCCGTTGTCCTTCTTCAGCCTCT146
ZX01G0052790AAGCGGAGATAGGAACGAACATAGCAGCAGAGAAGAGAAGAAGG122
ZX01G0121040ATCAGTGCGATGCGTCAGTTGTCGTAAGTCTTGCTCAGGAA114
ZX04G0012630TCCAACACCAACAGCAACACGTATTCAACTGCCTAACGAAGC188
ZX05G0014510GAACTCAAGAATCCATAGCAAGCATGAAGAGGAGAAGAGCAGTCAAGAA150
ZX06G0002180TTGGCAGTGATAGTTGTTGGTTGAGTCCGTGGAAGCATCGT156
ZX06G0012300TTAGTGGAAGAAGGTGAAGGTGAAGAAGTTGTTGTGCTTGAAGTATCTG147
ZX07G0010660CGCAGGAACTCATCGGTCAATGGTGTTGGCATGGATCTCTG179
ZX08G0002060CATTGCGTTGAAGTTGGAAGGTCCTCGTCATCTGCTGTTGCT183
), ArticleFig(id=1276531558014120050, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Tab. 2, caption=

Information of 26 HSF gene family members in passion fruit genome

, figureFileSmall=null, figureFileBig=null, tableContent=
基因ID Gene ID基因名称Gene name染色体Chromosome起始位置Start/bp终止位置End/bpDAN链DNAstrand氨基酸数目Number of amino acids分子量Molecular weight/(g·mol–1)等电点Isoelectric point
ZX01G0002530PeHSF118 125 2648 127 38527830 453.25.50
ZX01G0031130PeHSF2136 650 91536 652 35236340 377.08.36
ZX01G0033270PeHSF3137 846 33137 847 96921425 155.010.80
ZX01G0052790PeHSF4152 338 51752 340 35023126 844.27.92
ZX01G0052980PeHSF5152 437 22252 439 067+23126 870.28.22
ZX01G0097330PeHSF61196 488 976196 493 029+53860 346.74.43
ZX01G0116590PeHSF71222 639 747222 641 41433738 773.45.84
ZX01G0121040PeHSF81226 501 965226 514 578+1589177 157.87.64
ZX01G0125220PeHSF91232 190 295232 193 763+37841 574.74.25
ZX04G0001060PeHSF1042 286 2172 288 157-31535 432.85.52
ZX04G0002290PeHSF1144 010 9754 016 322+86695 458.45.24
ZX04G0003200PeHSF1244 837 4174 840 45045050 342.34.50
ZX04G0012630PeHSF13440 722 04140 725 557+10011 544.99.55
ZX04G0030270PeHSF144111 116 250111 118 797+35941 637.44.68
ZX05G0014510PeHSF15598 957 27498 960 19729131 652.76.30
ZX05G0014520PeHSF16598 984 93798 991 51163770 341.36.22
ZX06G0002180PeHSF17610 474 72810 478 16640145 808.54.74
ZX06G0012300PeHSF18667 773 17267 774 245+21525 004.79.83
ZX06G0026630PeHSF196110 588 691110 591 99627431 588.48.46
ZX07G0010660PeHSF20776 909 18276 910 613+39443 079.76.52
ZX08G0002060PeHSF2189 063 8489 066 494+35941 530.34.77
ZX08G0009900PeHSF22835 548 38835 550 721+37542 371.85.27
ZX08G0013320PeHSF23841 453 91141 455 248+34138 597.19.94
ZX08G0017710PeHSF24847 243 87547 247 55439444 973.45.38
ZX08G0024160PeHSF25853 331 98153 334 283+48454 373.65.11
ZX09G0006470PeHSF26932 699 61732 701 13731835 592.36.80
), ArticleFig(id=1276531558098006131, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=表2, caption=

西番莲基因组26个HSF基因家族成员基本信息

, figureFileSmall=null, figureFileBig=null, tableContent=
基因ID Gene ID基因名称Gene name染色体Chromosome起始位置Start/bp终止位置End/bpDAN链DNAstrand氨基酸数目Number of amino acids分子量Molecular weight/(g·mol–1)等电点Isoelectric point
ZX01G0002530PeHSF118 125 2648 127 38527830 453.25.50
ZX01G0031130PeHSF2136 650 91536 652 35236340 377.08.36
ZX01G0033270PeHSF3137 846 33137 847 96921425 155.010.80
ZX01G0052790PeHSF4152 338 51752 340 35023126 844.27.92
ZX01G0052980PeHSF5152 437 22252 439 067+23126 870.28.22
ZX01G0097330PeHSF61196 488 976196 493 029+53860 346.74.43
ZX01G0116590PeHSF71222 639 747222 641 41433738 773.45.84
ZX01G0121040PeHSF81226 501 965226 514 578+1589177 157.87.64
ZX01G0125220PeHSF91232 190 295232 193 763+37841 574.74.25
ZX04G0001060PeHSF1042 286 2172 288 157-31535 432.85.52
ZX04G0002290PeHSF1144 010 9754 016 322+86695 458.45.24
ZX04G0003200PeHSF1244 837 4174 840 45045050 342.34.50
ZX04G0012630PeHSF13440 722 04140 725 557+10011 544.99.55
ZX04G0030270PeHSF144111 116 250111 118 797+35941 637.44.68
ZX05G0014510PeHSF15598 957 27498 960 19729131 652.76.30
ZX05G0014520PeHSF16598 984 93798 991 51163770 341.36.22
ZX06G0002180PeHSF17610 474 72810 478 16640145 808.54.74
ZX06G0012300PeHSF18667 773 17267 774 245+21525 004.79.83
ZX06G0026630PeHSF196110 588 691110 591 99627431 588.48.46
ZX07G0010660PeHSF20776 909 18276 910 613+39443 079.76.52
ZX08G0002060PeHSF2189 063 8489 066 494+35941 530.34.77
ZX08G0009900PeHSF22835 548 38835 550 721+37542 371.85.27
ZX08G0013320PeHSF23841 453 91141 455 248+34138 597.19.94
ZX08G0017710PeHSF24847 243 87547 247 55439444 973.45.38
ZX08G0024160PeHSF25853 331 98153 334 283+48454 373.65.11
ZX09G0006470PeHSF26932 699 61732 701 13731835 592.36.80
), ArticleFig(id=1276531558194475124, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Tab. 3, caption=

Distribution of passion fruit HSF gene in duplicate regions

, figureFileSmall=null, figureFileBig=null, tableContent=
重复区Duplicate region重复1 Duplication 1重复2 Duplication 2
染色体Chromosome位置Position/bp基因Gene染色体Chromosome位置Position/bp基因Gene
1Chr137 846 331~37 847 969ZX01G0033270Chr1222 639 747~222 641 414ZX01G0116590
2Chr152 338 517~52 340 350ZX01G0052790Chr152 437 222~52 439 067ZX01G0052980
3Chr137 846 331~37 847 969ZX01G0033270Chr847 243 875~47 247 554ZX08G0017710
4Chr1222 639 747~222 641 414ZX01G0116590Chr847 243 875~47 247 554ZX08G0017710
), ArticleFig(id=1276531558269972597, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=表3, caption=

西番莲HSF基因在重复片段区域的分布

, figureFileSmall=null, figureFileBig=null, tableContent=
重复区Duplicate region重复1 Duplication 1重复2 Duplication 2
染色体Chromosome位置Position/bp基因Gene染色体Chromosome位置Position/bp基因Gene
1Chr137 846 331~37 847 969ZX01G0033270Chr1222 639 747~222 641 414ZX01G0116590
2Chr152 338 517~52 340 350ZX01G0052790Chr152 437 222~52 439 067ZX01G0052980
3Chr137 846 331~37 847 969ZX01G0033270Chr847 243 875~47 247 554ZX08G0017710
4Chr1222 639 747~222 641 414ZX01G0116590Chr847 243 875~47 247 554ZX08G0017710
), ArticleFig(id=1276531558345470070, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=EN, label=Tab. 4, caption=

Expression levels and differences of 12 HSF genes in passion fruit

, figureFileSmall=null, figureFileBig=null, tableContent=
基因Gene组织Tissue表达水平(TPM)Expression level (TPM)Log2FCP adjust显著性Significance调控作用Regulation
金陵紫果Jinlingziguo黄果原生种Huangguo original species
ZX05G0014520茎秆3.3371.8830.9000.005noup
花蕾5.07323.683–1.9007.53E–10yesdown
叶片8.9774.1171.2720.094noup
卷须5.8073.3470.8010.166noup
ZX08G0002060茎秆0.0300.0101.5281.000noup
花蕾0.1330.207–0.3550.787nodown
叶片0.1070.0401.5370.811noup
卷须0.1170.0800.6030.865noup
ZX08G0024160茎秆7.1106.9400.1070.821noup
花蕾6.6079.343–0.1980.571nodown
叶片5.3435.8430.0150.994noup
卷须8.2008.683–0.0460.943nodown
ZX01G0002530茎秆3.5172.1900.7260.463noup
花蕾8.78337.660–1.7510.014yesdown
叶片2.8871.6570.9360.092noup
卷须22.53315.8070.5160.627noup
ZX07G0010660茎秆3.3334.397–0.2820.642nodown
花蕾3.87010.893–1.2691.80E–05yesdown
叶片2.6933.880–0.2180.855nodown
卷须6.6239.480–0.4660.324nodown
ZX01G0121040茎秆56.82782.173–0.4430.011nodown
花蕾46.123116.893–1.0281.17E–11yesdown
叶片45.00797.533–0.8795.10E–10nodown
卷须78.453133.823–0.7280.018nodown
ZX04G0012630茎秆2.0331.6270.3880.498noup
花蕾2.0975.103–0.9820.005nodown
叶片2.0302.687–0.2680.824nodown
卷须2.9603.217–0.0720.945nodown
ZX06G0002180茎秆5.2775.5770.0470.939noup
花蕾5.57016.490–1.3143.84E–05yesdown
叶片6.9677.0870.1260.941noup
卷须6.1407.933–0.2670.744nodown
ZX01G0052790茎秆0.0330.230–2.8010.343nodown
花蕾0.1103.650–4.6733.89E–07yesdown
叶片0.0000.123–3.6101.000nodown
卷须0.2170.923–1.9880.238nodown
ZX05G0014510茎秆0.0600.737–3.6200.010yesdown
花蕾0.13322.727–7.1281.95E–33yesdown
叶片0.0170.507–4.8430.026yesdown
卷须0.2071.967–3.0360.042yesdown
ZX01G0052980茎秆0.1130.0003.6881.000noup
花蕾0.6830.0006.3770.001yesup
叶片0.0000.0000.0001.000no testno test
卷须0.4830.0005.5550.011yesup
ZX06G0012300茎秆0.0730.0400.8921.000noup
花蕾0.5930.0803.1090.128noup
叶片0.0730.0400.9341.000noup
卷须0.4230.0473.2110.325noup
), ArticleFig(id=1276531558433550455, tenantId=1146029695717560320, journalId=1235980609244409860, articleId=1276531539429158920, language=CN, label=表4, caption=

12个HSF基因在西番莲中的表达水平及差异

, figureFileSmall=null, figureFileBig=null, tableContent=
基因Gene组织Tissue表达水平(TPM)Expression level (TPM)Log2FCP adjust显著性Significance调控作用Regulation
金陵紫果Jinlingziguo黄果原生种Huangguo original species
ZX05G0014520茎秆3.3371.8830.9000.005noup
花蕾5.07323.683–1.9007.53E–10yesdown
叶片8.9774.1171.2720.094noup
卷须5.8073.3470.8010.166noup
ZX08G0002060茎秆0.0300.0101.5281.000noup
花蕾0.1330.207–0.3550.787nodown
叶片0.1070.0401.5370.811noup
卷须0.1170.0800.6030.865noup
ZX08G0024160茎秆7.1106.9400.1070.821noup
花蕾6.6079.343–0.1980.571nodown
叶片5.3435.8430.0150.994noup
卷须8.2008.683–0.0460.943nodown
ZX01G0002530茎秆3.5172.1900.7260.463noup
花蕾8.78337.660–1.7510.014yesdown
叶片2.8871.6570.9360.092noup
卷须22.53315.8070.5160.627noup
ZX07G0010660茎秆3.3334.397–0.2820.642nodown
花蕾3.87010.893–1.2691.80E–05yesdown
叶片2.6933.880–0.2180.855nodown
卷须6.6239.480–0.4660.324nodown
ZX01G0121040茎秆56.82782.173–0.4430.011nodown
花蕾46.123116.893–1.0281.17E–11yesdown
叶片45.00797.533–0.8795.10E–10nodown
卷须78.453133.823–0.7280.018nodown
ZX04G0012630茎秆2.0331.6270.3880.498noup
花蕾2.0975.103–0.9820.005nodown
叶片2.0302.687–0.2680.824nodown
卷须2.9603.217–0.0720.945nodown
ZX06G0002180茎秆5.2775.5770.0470.939noup
花蕾5.57016.490–1.3143.84E–05yesdown
叶片6.9677.0870.1260.941noup
卷须6.1407.933–0.2670.744nodown
ZX01G0052790茎秆0.0330.230–2.8010.343nodown
花蕾0.1103.650–4.6733.89E–07yesdown
叶片0.0000.123–3.6101.000nodown
卷须0.2170.923–1.9880.238nodown
ZX05G0014510茎秆0.0600.737–3.6200.010yesdown
花蕾0.13322.727–7.1281.95E–33yesdown
叶片0.0170.507–4.8430.026yesdown
卷须0.2071.967–3.0360.042yesdown
ZX01G0052980茎秆0.1130.0003.6881.000noup
花蕾0.6830.0006.3770.001yesup
叶片0.0000.0000.0001.000no testno test
卷须0.4830.0005.5550.011yesup
ZX06G0012300茎秆0.0730.0400.8921.000noup
花蕾0.5930.0803.1090.128noup
叶片0.0730.0400.9341.000noup
卷须0.4230.0473.2110.325noup
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西番莲HSF基因家族的全基因组鉴定及成花期对高温胁迫的响应
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吴艳艳 1, * , 刘洁云 1 , 周俊妞 1 , 田青兰 1 , 黄伟华 1 , 朱陈利 2 , 牟海飞 1, *
热带作物学报 | 组学与生物技术 2025,46(4): 807-819
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热带作物学报 |组学与生物技术 2025 , 46 (4) : 807 -819
西番莲HSF基因家族的全基因组鉴定及成花期对高温胁迫的响应
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吴艳艳1, * , 刘洁云1, 周俊妞1, 田青兰1, 黄伟华1, 朱陈利2, 牟海飞1, *
作者信息
  • 1.广西壮族自治区农业科学院生物技术研究所,广西南宁 530007
  • 2.广西壮族自治区农业科学院,广西南宁 530007
通讯作者:
* 牟海飞(MOU Haifei),E-mail:
吴艳艳(WU Yanyan),E-mail:
Genome-wide Identification of HSF Gene Family and Their Response to Hot Ambient Temperature During Flower Development in Passion Fruit (Passiflora edulis)
Yanyan WU1, * , Jieyun LIU1, Junniu ZHOU1, Qinglan TIAN1, Weihua HUANG1, Chenli ZHU2, Haifei MOU1, *
Affiliations
  • 1.Biotechnology Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi 530007, China
  • 2.Guangxi Academy of Agricultural Sciences, Nanning, Guangxi 530007, China
出版时间: 2025-04-25 doi: 10.3969/j.issn.1000-2561.2025.04.004
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热激转录因子(heat shock transcription factor,HSF)是重要的调节因子,在植物响应高温胁迫中发挥重要作用。高温胁迫对西番莲成花造成了严重的负面影响,因此研究HSF调控西番莲耐热性的意义重大。本研究利用生物信息学技术在西番莲基因组上鉴定了26个热激转录因子基因,分别命名为PeHSF1~PeHSF26。西番莲HSF基因编码蛋白长度为100~1589个氨基酸,分子量为11 544.9~177 157.8 g/mol,理论等电点为4.25~10.80。西番莲26个HSF基因分布在第1、4、5、6、7、8和9染色体上,分为10个亚群。西番莲全基因组复制事件分析结果表明,ZX01G0033270ZX01G0052790ZX01G0052980等5个HSF基因位于重复片段内。西番莲HSF基因有1~12个内含子和2~13个外显子,都包含HSF-DNA结合结构域。利用RNA-seq分析黄果原生种与金陵紫果HSF基因对高温环境的响应,发现ZX01G0002530ZX01G0052790ZX01G0121040等基因在花蕾中表达量差异显著,并通过RT-qPCR验证候选HSF基因表达水平。综合分析,推测西番莲响应高温胁迫的最理想的候选HSF基因为ZX01G0121040。这些结果有助于了解HSF在西番莲成花期响应高温胁迫过程中的功能,为西番莲耐高温的遗传改良提供重要基因资源和理论依据。

西番莲  /  高温胁迫  /  热激转录因子  /  同源基因  /  成花  /  转录组测序  /  候选基因

Heat shock transcription factor (HSF) is an important regulatory factor that plays a crucial role in plant response to hot ambient temperature (HAT). High temperature stress has a serious negative impact on the flowering of passion fruit, therefore, studying the regulation of heat tolerance by HSF in passion fruit is of great significance. In this study, we identified 26 HSF genes on the genome of passion fruit using bioinformatics technology, named PeHSF1-PeHSF26. The genes could encode proteins of 100-1589 amino acids, with molecular weight 11 544.9-177 157.8 g/mol, and a theoretical isoelectric point of 4.25-10.80. The 26 genes were distributed on chromosomes 1, 4, 5, 6, 7, 8 and 9, and were divided into 10 subpopulations. The analysis of the whole genome replication event showed that ZX01G0033270, ZX01G0052790 and ZX01G0052980 were located within the genome duplications. The genes contained 1-12 introns and 2-13 exons, all contained HSF-DNA binding domains. RNA-seq analysis of Huangguo original species and Jinlingziguo HSF genes to HAT revealed that there were significant differences in the expression levels of genes, including ZX01G0002530, ZX01G0052790 and ZX01G0121040 in flower buds. The expression levels of candidate HSF genes were validated by RT-qPCR. Based on comprehensive analysis, it is supposed that the most ideal candidate HSF gene for passion flower response to high temperature stress was ZX01G0121040. The results would contribute to understand the function of HSF in response to high temperature stress during the flowering of passion fruit, and provide important genetic resources and theoretical basis for genetic improvement of passion fruit.

passion fruit  /  hot ambient temperature  /  heat shock factor  /  orthologous gene  /  flowering  /  RNA sequencing  /  candidate gene
吴艳艳, 刘洁云, 周俊妞, 田青兰, 黄伟华, 朱陈利, 牟海飞. 西番莲HSF基因家族的全基因组鉴定及成花期对高温胁迫的响应. 热带作物学报, 2025 , 46 (4) : 807 -819 . DOI: 10.3969/j.issn.1000-2561.2025.04.004
Yanyan WU, Jieyun LIU, Junniu ZHOU, Qinglan TIAN, Weihua HUANG, Chenli ZHU, Haifei MOU. Genome-wide Identification of HSF Gene Family and Their Response to Hot Ambient Temperature During Flower Development in Passion Fruit (Passiflora edulis)[J]. Chinese Journal of Tropical Crops, 2025 , 46 (4) : 807 -819 . DOI: 10.3969/j.issn.1000-2561.2025.04.004
栽培种西番莲(又名百香果)为草质藤本植物,其果实具有芳香气味,且富含糖类、维生素及钙、铁、锌等矿物质元素,营养价值极高,深受消费者青睐。温度是影响植物生长、发育的重要外界因素之一。NAVE等[1]研究表明在长日照条件下西番莲品种Passion Dream(黄果西番莲与紫果西番莲的杂交种)成花最佳温度为22℃/16℃(日/夜),温度高于28℃环境下任何光周期改变都不会观察到西番莲成花。这表明西番莲成花期对高温环境的耐受性较差,从而造成减产,是影响西番莲生产的重要问题。
热激转录因子(heat shock transcription factor,HSF)是一类调控植物热激反应的转录因子。热激转录因子基因序列由5个部分组成:(i)DNA结合区域DBD;(ii)寡聚化结构域OD;(iii)核定位信号NLS;(iv)核输出信号NES;(v)C末端激活结构域AHA[2],其中DBD是所有结构域中最保守的区域,能够识别热反应基因启动子的顺式元件[3]。PELHAM等[4]首次在酵母中鉴定了热激转录因子。随着多个物种高质量参考基因组公布,研究人员已经在拟南芥(21)、水稻(25)、番茄(26)、甘蓝(52)、辣椒(25)、胡萝卜(35)、葡萄(19)、柑橘(18)、苹果(23)、草莓(17)、杨树(31)、大豆(52)、高粱(24)、玉米(22)、小麦(61)、芝麻(30)、木薯(32)等鉴定了HSF基因[2,5]。最近,YU等[5]利用111种植物全基因组,共鉴定了2950个HSF基因,构建了植物HSF基因数据库(http://hsfdb.bio2db.com/),这为人们研究植物HSF基因功能提供了便利。前人研究表明,热激蛋白及热激转录因子在植物成花过程中起着重要调节作用。在拟南芥中,热激蛋白HSP90与关键开花调节因子LFY、SOC1和AGL24相互作用,促进开花[6]。热激转录因子HSFA2与拟南芥对高温的传代记忆,促使植物提前开花[7]。在番茄中,热激转录因子调控花蕾对高温的响应[8]。因此,利用西番莲基因组鉴定热激转录因子,揭示在高温胁迫环境中其对成花的影响十分必要。
2021年,MA等[9]成功组装了高质量西番莲基因组,本研究利用生物信息学方法从西番莲基因组中鉴定了HSF家族成员,构建了模式植物及重要耐热植物的HSF系统进化树,分析了西番莲HSF基因在花蕾、叶片等组织部位的表达模式,推测可能影响西番莲成花期耐热性基因,本研究将促进人们对西番莲适应高温环境机制的认知,为西番莲耐高温育种提供重要基因资源和理论基础。
2022年4月2日,高温耐受西番莲品种金陵紫果(ZG)和敏感品种黄果原生种(HG)种植于广西南宁市美丽南方试验地高温处理设施内。
用钢管制成长(10.0 m)×宽(2.0 m)×高(4.0 m)的生长棚框架,固定于沟面,于高温处理开始时通过在生长棚框架四周覆盖塑料薄膜(透光率95%以上)进行升温,大棚两侧上部各均匀留出20 cm高的空隙,用于气体交换。高温处理结束后将薄膜升起,后期管理及田间小气候与对照一致。热处理前将增温棚处于全部打开状态,与对照处于同一自然环境条件,于植株二级蔓抽出开始高温热胁迫处理,将增温棚顶部和侧面膜放下,并实时监测棚内温度,直至达到高温设定值,即热胁迫处理日最高温度38~45 ℃,日平均温度30~31 ℃,日温度≥35 ℃持续时间4~6 h;自然对照日最高温度<37 ℃,日平均温度<28.5 ℃,日温度≥35 ℃持续时间<2 h。40 d后结束热处理。处理结束后,在中午12:00取样,包括花蕾、卷须、叶片和茎(图1)。
基于热激转录因子的特异氨基酸序列(Pfam: PF00447),在紫果西番莲基因组数据库(https://db.cngb.org/search/assembly/CNA0017758/)下载蛋白序列,使用PfamScan软件将西番莲的蛋白序列在Pfam数据库中进行检索,鉴定西番莲HSF家族成员。采用相同方法,在水稻(Oryza sativa L. japonicahttp://rice.uga.edu/)、拟南芥(Arabidopsis thalianahttps://www.arabidopsis.org/index.jsp)、番茄(Solanum lycopersicumhttp://plants.ensembl.org/Solanum_lycopersicum/Info/Index)、单瓣茉莉花(Jasminum sambachttps://ngdc.cncb.ac.cn/gwh/Assembly/22882/show)、木薯(Manihot esculentahttps://cbi.gxu.edu.cn/yxguo/DockingDB/download_files/data/)、玉米(Zea mayshttp://plants.ensembl.org/Zea_mays/Info/Index)数据库中鉴定6个物种的HSF家族成员。
使用在线软件ProtParam(https://web.expasy.org/protparam/)预测西番莲HSF蛋白的长度、分子量和等电点。
将西番莲、水稻、拟南芥、番茄、单瓣茉莉花、木薯(单倍型A和B基因组)和玉米的HSF成员的蛋白序列合并输入到MUSCLE进行全局比对,比对结果使用MEGA 7程序构建maximal likelihood似然树,设置bootstrap重复次数为1000次,最后输入iTOL在线软件(https://itol.embl.de/)进行美化。
基因结构:从GFF文件中提取HSF基因的外显子、内含子位置信息,从Pfam注释结果中提取motif信息,使用GSDS程序绘制如下基因结构及motif分布图。共线性分析:首先BLAST比对所有蛋白序列,设定阈值E<1e-5,最小覆盖度大于40%。比对结果输入MCScanX程序,参数默认,输出全基因组范围内的共线性区块,并标注位于这些共线性区块内的目标基因家族。最后,用Circos在线软件(https://circos.ca/intro/tabularvisualization/)绘图。
利用TRIzol® Reagent试剂盒提取total RNA(Invitrogen,USA),具体流程按照说明书操作。OligodT富集mRNA,片段化mRNA,反转合成cDNA和连接adaptor参照前期发表文献的试验操作进行[10]
采用Illumina NovaSeq6000测序平台完成转录组测序,构建Illumina PE文库进行2×150 bp测序,通过fastp软件对获得的测序数据进行质量控制,包括:(1)碱基错误率分布统计;(2)碱基含量分布统计。将质控后的原始数据,即clean data(reads),利用Hisat2软件与参考基因组比对,参考基因组来自https://db.cngb.org/search/assembly/CNA0017758/。随后,获得mapped reads,同时利用RSeQC-2.3.6软件对转录组测序的比对结果进行质量评估,主要包括测序饱和度、基因覆盖度、reads在参考基因组不同区域分布以及reads在不同染色体分布分析。使用StringTie软件对每个样本进行拼接,最终合并在一起。
使用RSEM软件(http://deweylab.github.io/RSEM/)分别对基因/转录本的整体表达水平进行定量分析,以便后续分析不同样本间基因/转录本的差异表达情况,定量指标为TPM(transcripts per million reads)。基因表达量分析获得基因/转录本的read counts数量后,采用DESeq2对多样本项目进行样本间或组间基因/转录本差异表达分析,鉴定出差异表达的基因/转录本,设置参数:P adjust<0.05并且|log2FC|≥1。
利用聚类热图在线软件(https://cloud.oebiotech.cn/task/detail/heatmap/)展示西番莲HSF基因的表达量及相关性,数据归一化方式为row。
采用Trizol法提取金陵紫果和黄果原生种花蕾的总RNA,利用HiScriptⅡQ RT SuperMix for qPCR(+gDNA wiper)试剂盒进行反转录。实时荧光定量PCR反应采用Universal SYBR qPCR Master法,反应体系(20 μL):10 μL Universal SYBR qPCR Master Mix,0.5 μL上游引物,0.5 μL下游引物,1 μL cDNA,8 μL ddH2O。反应条件为94 ℃预变性3 min;94 ℃变性15 s,58 ℃退火15 s,72 ℃延伸20 s,40个循环;设置3个重复。荧光定量PCR相关引物见表1
基于HSF保守结构域(PF00447)氨基酸序列信息,利用PfamScan软件在西番莲、拟南芥、水稻、番茄、单瓣茉莉花、木薯和玉米中分别检测到26、24、25、26、23、63个(单倍型A基因组32个,单倍型B基因组31个)、玉米26个。西番莲HSF基因分布在第1、4、5、6、7、8、9染色体上,其中第1染色体上的HSF基因数量最多,为9个,而第2和3染色体上未鉴定出HSF基因,说明HSF基因在西番莲基因组上分布不均匀。西番莲的26个HSF基因平均长度为3062 bp,其中ZX06G0012300长度最小,为1073 bp;ZX01G0121040的长度最大,为12 613 bp;13个HSF基因分布在正义链上,13个在反义链上(表2)。依据西番莲26个HSF基因在基因组上的位置,将其命名为PeHSF1~PeHSF26。理化性质分析结果显示,西番莲HSF基因编码的氨基酸数量为100~1589,分子量为11 544.9~177 157.8 g/mol,预测等电点为4.25~10.80(表2)。
基于西番莲的26个HSF蛋白的氨基酸序列,利用MUSCLE软件进行全局比对,比对结果输入MEGA 7构建最大似然树。根据进化关系,将26个HSF基因分为10个亚群体,其中亚群Ⅱ包含5个HSF基因,亚群Ⅲ仅有1个HSF基因(图2A)。为了解不同物种间HSF基因的进化关系,基于西番莲等7个物种213个HSF蛋白构建了进化树,共分为11个亚群(图2B)。木薯是热带地区广泛种植的作物,其基因组大小为687 Mb[11],包含32个HSF基因。单瓣茉莉花是一种常绿植物,在夏季38 ℃以上的高温也可开花[12],因此,了解茉莉花耐高温胁迫分子机有助于预测西番莲HSF基因的功能。
利用26个HSF基因分析片段重复事件,结果表明有4个大的基因组重复区,包含5个HSF基因,分别为ZX01G0033270ZX01G0052790ZX01G0052980ZX01G0116590ZX08G0017710。具体信息是:(i)第1染色体上37 846 331~37 847 969 bp对应第1染色体上222 639 747~222 641 414 bp;(ii)第1染色体上52 338 517~52 340 350 bp对应第1染色体上52 437 222~52 439 067 bp;(iii)第1染色体上37 846 331~37 847 969 bp对应第8染色体上47 243 875~47 247 554 bp;(iv)第1染色体上222 639 747~222 641 414 bp对应第8染色体上47 243 875~47 247 554 bp(表3图3)。
由于西番莲基因组共线性区域的HSF仅有5个,无法推测全基因组复制(whole genome duplication,WGD)事件,因此使用MCScanX软件鉴定处于基因组共线性区块内4对同源基因,计算每个同源基因对的Ka、Ks、Ka/Ks值,Ks值越高表明基因组复制速度越快。一般认为Ks=1.5处为双子叶植物共同经历的六倍化事件(距今约110百万年),随后西番莲经过2次独立的全基因组复制事件WGD-1和WGD-2(图4)。
通过基因结构分析可以了解西番莲HSF基因家族成员的进化关系。本研究对26个HSF基因进行基因结构分析,从内含子-外显子组成来看,PeHSF基因有1~12个内含子和2~13个外显子(图5)。26个西番莲HSF基因均含有DNA结合保守结构域,这与前人研究结果一致[3]ZX01G0121040除了含有DNA结合保守结构域之外,还有SNARE、Syntaxin 2、PPR、PPR1、PPR2结构域,ZX05G0014520还含有RCCR结构域,ZX04G0002290含有SurE结构域。
由于高温敏感品种黄果原生种和高温耐受品种金陵紫果在夏天高温环境中成花差异(图6),因此,可以2个品种的叶片(leaf,L)、卷须(tendril,T)、花蕾(flower,F)和茎(stem,S)进行转录组分析,找出影响西番莲耐热差异的基因。
将高温处理后采集的24个样品测序,测序数据质量控制后有效读长(clean reads)数为41 725 898~52 997 150条,有效碱基数为6 058 511 181~7 620 631 463 bp,测序碱基正确率在99.9%(Q30)以上的碱基占总碱基的百分比为92.34%~93.70%(附表1)。
将质控后有效读长与西番莲参考基因组比对(https://db.cngb.org/search/assembly/CNA0017758/),能定位到基因组上的有效读长数为30 464 977~41 566 866,比对率为72.47%~78.63%,平均比对率为76.72%;在参考序列上有多个比对位置的有效读长数为1 706 379~3 969 640,比对率为3.75%~9.31%;在参考序列上有唯一比对位置的clean reads数目为28 682 624~37 830 849,比对率为67.86%~72.20%(附表2)。
利用RSEM软件分别对基因和新转录本的表达水平进行定量分析,定量指标为TPM(transcripts per million),24个样品的基因表达量见附表3。基于基因表达量,分析24个样本间的相关系数,结果显示样本生物学重复性好。通过PCA分析发现,生物学重复间的样本间相似性高(图7)。
采用DESeq2软件进行组间基因表达量差异分析,获得2组间发生差异表达的基因(DEGs)。在接种0 h时,HG与ZG的花蕾间的差异表达基因共有6077个,其中3363个上调基因,2714个下调基因;卷须间的差异表达基因共有1923个,其中1091个上调基因,832个下调基因;茎秆间的差异表达基因共有1833个,其中1023个上调基因,860个下调基因;叶片间的差异表达基因共有1592个,其中848个上调基因,744个下调基因(图8,附表4)。
分析26个HSF基因在紫果和黄果原生种中的表达量(TPM),结果表明ZX01G0002530ZX01G0052790ZX01G0052980ZX01G0121040ZX05G0014510ZX05G0014520ZX06G0002180ZX07G0010660在花蕾的表达量差异显著(表4图9)。与黄果原生种相比,ZX05G0014520ZX08G0002060、ZX01G0002530在金陵紫果的叶片、卷须和茎秆中表达量上调;虽然ZX07G0010660ZX01G0121040ZX01G0052790在叶片、花蕾和茎秆中表达量下调,但是仅在花蕾中达到显著性差异,且ZX01G0121040基因的表达水平高(表4)。
由于ZX01G0052980ZX01G0055790之间以及ZX05G0014510ZX05G0014520之间的序列高度相似,不利于设计引物,本研究利用RT-qPCR技术检测ZX01G0002530ZX01G0052790ZX01G1G0121040ZX04G0012630ZX05G0104150ZX006G0002180ZX09G0012300ZX07G0010660、ZX08G00002060ZX08G0024160在黄果原生种和金陵紫果花蕾的表达量(图10)。RT-qPCR分析结果表明,10个HSF基因在黄果原生种与金陵紫果的表达水平与RNA-seq分析的结果一致。值得注意的是,仅有ZX06G0012300在金陵紫果的表达水平高于黄果原生种。
热应激转录因子是植物热胁迫防御响应中的中心调节子。目前,研究人员在水稻、拟南芥和番茄中发现HSF基因参与调控高温环境响应。GUO等[13]在拟南芥和水稻基因组中分别鉴定出21个和25个HSF基因,YANG等[14]在番茄(Solanum lycopersicum)中鉴定出26个HSF基因。本研究中,在拟南芥、水稻和番茄基因组中分别鉴定到24、25、26个HSF基因,与GUO等[13]鉴定的拟南芥HSF基因数量有差异。YU等[5]构建了111种植物HSF耐热基因数据库,其中拟南芥基因组含有24个HSF基因,这与本研究结果一致。根据Ensembl Plants数据库收录的信息,水稻、拟南芥和番茄基因组大小分别为373.8、119.7、827.4 Mb。虽然番茄基因组大小是拟南芥的6.9倍,但它们的HSF基因数量仅相差2个,这表明HSF基因可能在植物适应高温环境中功能保守。因此,借鉴水稻、拟南芥和番茄的HSF基因功能,推测西番莲HSF基因作用。
在拟南芥中,热激转录因子基因HsfA1aAt4g17750)是响应热胁迫的主要调控因子[15-16]。在本研究中,进化树分析结果表明西番莲ZX01G0121040HsfA1a亲缘关系较近,属于亚群Ⅳ。此外,该亚群还包括拟南芥其他4个HSF基因,分别为At1g67970At1g32330At3g02990At5g16820At1g32330HSFA1d)和At5g16820HSFA1b)属于HSFA1s亚家族,它们是拟南芥热形态建成所必需的[17],而AT3G02990HSFA1e)似乎对热响应不那么重要[16]。此外,LOC_Os03g12370OsHsfA9)和LOC_Os03g63750OsHsfA1a)也属于亚群Ⅳ,在水稻热胁迫时表达量显著上调[18]
我们发现西番莲经历3次全基因组复制事件,这与ZHENG等[19]的研究结果一致。在西番莲基因组中,有5个HSF基因位于基因组复制区域,其中ZX01G0033270ZX01G0116590ZX08G0017710聚类在亚群Ⅲ。亚群Ⅲ含有拟南芥HSF基因:At3g51910HSFA7a)、At3g63350HSFA7b)和At3g22830,研究表明NAC019结合HSFA1bHSFA6bHSFA7aHSFC1的启动子而增强了拟南芥耐热性[20]。HSFA7b通过调节拟南芥中乙烯的生物合成和信号传导来控制茎尖分生组织的温度变化[21]。此外,亚群Ⅲ还包含水稻HSF基因LOC_Os03g58160LOC_Os07g08140LOC_Os03g53320LOC_Os03g53340LOC_Os10g28340LOC_Os03g06630HTG3),其中HTG3通过调节JAZ参与水稻的耐热性[22]ZX01G0052790ZX01G0052980聚类在一起,属于亚群Ⅺ,该亚群包含有2个拟南芥基因:At2g41690HSFB3)和At4g36990HsfB1)。研究表明,RCF3正调控HSFA1eHSFA3HSFA9HSFB3DREB2C的表达增加拟南芥的耐热性[23]。虽然HsfB1HsfB2b抑制HsfA2HsfA7aHsfB1HsfB2b表达,但是正调控拟南芥的耐热性[24]
利用RNA-seq分析发现有12个HSF基因在黄果原生种和金陵紫果花蕾的表达量差异显著,进化树分析表明ZX01G0121040与拟南芥的HsfA1a基因亲缘关系较近,HsfA1a正调控热胁迫[15-16]ZX01G0002530、ZX01G0052790、ZX01G0052980、ZX05G0014510ZX05G0014520属于亚群Ⅺ,且ZX01G0052790ZX05G0014510表达模式相似。虽然ZX01G0052790ZX01G0052980基因序列具有共线性,但是它们在西番莲花蕾响应高温时的表达量趋势相反。HSFB3HsfB1位于亚群Ⅺ内,均与拟南芥的耐热性相关[23-24]ZX04G0012630ZX06G0002180ZX08G0024160属于亚群Ⅶ,该亚群中At4g18870参与调控拟南芥的耐热性[25]。在系统进化树上,ZX06G0002180At4g18870的亲缘关系更近。ZX07G0010660属于亚群Ⅹ,同源基因At4g11660HsfB2b)正调控拟南芥的耐热性[24]ZX08G0002060属于亚群Ⅳ,其同源基因At3g22830HSFA6b)参与ABA介导的耐热性[26],另一同源基因HSFA7A可能参与了拟南芥对高温的适应[20,24]
本研究发现,西番莲HSF基因除了含有DNA结合结构域外,ZX01G0121040还包含有PPR、Syntaxin 2和SNARE等结构域。PPR(pentatricopeptide repeat)是一种三角状五肽重复蛋白,属于植物中最大的核编码蛋白家族。PPR蛋白参与植物生长发育和响应胁迫反应[27-28]。Qa-SNARE最早在哺乳动物基因组中发现,命名为突触融合蛋白(syntaxin),其在与植物体生长发育、抗病反应和非生物胁迫中起着重要功能[29-30]。此外,ZX05G0014520还含有RCCR结构域,RCCR是催化叶绿素降解代谢反应的主要酶类[31]。这些研究结果表明,西番莲HSF基因可能在植物生长发育和逆境胁迫中也具有重要功能。
高温胁迫严重影响了西番莲的成花,鉴定耐热基因是提高西番莲适应极端温度的一个有效方法。在本研究中,我们在西番莲基因组中鉴定了26个HSF基因,并分析了HSF成员的理化性质、进化树、基因结构、共线性和全基因组复制事件。利用RNA-seq分析发现ZX01G0002530ZX01G0052790ZX01G0052980ZX01G0121040ZX04G0012630ZX05G0014510ZX05G0014520ZX06G0002180ZX06G0012300ZX07G0010660ZX08G0002060ZX08G0024160在金陵紫果与黄果原生种花蕾的表达量差异显著,RT-qPCR分析结果验证了RNA-seq的结果,并推测ZX01G0121040是西番莲成花期响应高温胁迫的重要基因。本研究结果将为西番莲成花耐热性的遗传改良提供重要的基因资源和理论技术支撑。
  • 国家自然科学基金项目(32260740; 32060660)
  • 广西自然科学基金项目(2023GXNSFAA026301)
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2025年第46卷第4期
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doi: 10.3969/j.issn.1000-2561.2025.04.004
  • 接收时间:2024-11-29
  • 首发时间:2026-06-24
  • 出版时间:2025-04-25
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  • 收稿日期:2024-11-29
  • 录用日期:2024-12-19
基金
国家自然科学基金项目(32260740; 32060660)
广西自然科学基金项目(2023GXNSFAA026301)
作者信息
    1.广西壮族自治区农业科学院生物技术研究所,广西南宁 530007
    2.广西壮族自治区农业科学院,广西南宁 530007

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* 牟海飞(MOU Haifei),E-mail:
吴艳艳(WU Yanyan),E-mail:
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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