Article(id=1304388207668388458, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.12.023, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1764604800000, receivedDateStr=2025-12-02, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919983068, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919983068, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919983068, creator=13701087609, updateTime=1788919983068, updator=13701087609, issue=Issue{id=1304388108988997783, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='12', pageStart='4509', pageEnd='4948', issueExtLink='null', onlineDate='null', pubDate='1782576000000', pubDateStr='2026-06-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919959542, creator='13701087609', updateTime=1788923461082, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402795579330582, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402795579330583, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=4811, endPage=4822, ext={EN=ArticleExt(id=1304388208389808748, articleId=1304388207668388458, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Identification of Panax ginseng FAD gene family based on T2T genome and functional verification of PgFAD2-56, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective FAD enzymes introduce double bonds at specific positions in fatty acids, converting saturated fatty acids into unsaturated fatty acids, playing crucial roles in plant growth, development, and stress responses. This study aimed to systematically identify the FAD gene family in Panax ginseng and verify the function of PgFAD2-56, so as to elucidate the functions and stress response mechanisms of ginseng FAD genes. Methods Using bioinformatics approaches, 98 PgFAD genes were identified from the P. ginseng T2T genome, and their physicochemical properties, phylogenetic relationships, chromosomal localization, gene structures, conserved motifs, cis-acting regulatory elements, collinearity, and expression patterns under stress conditions were analyzed. Molecular docking was performed to predict the binding affinity of highly expressed FAD2 proteins with oleic acid, and the function of PgFAD2-56 was verified using a yeast heterologous expression system. Results The results showed that the 98 PgFAD genes could be classified into six subfamilies (ADS, SLD, FAD3/FAD7/FAD8, FAD6, FAD2, and FAB) based on amino acid sequence similarity, which was consistently supported by their gene structures and conserved motifs. Numerous hormone- and stress-responsive cis-acting elements and transcription factor binding sites (TFBSs) were identified in the promoters of PgFAD genes. Collinearity analysis revealed significant expansion of the FAD2 subfamily in P. ginseng. Gene expression analysis demonstrated that some PgFADs displayed significant differential expression under stress conditions. Molecular docking indicated that FAD2-56 exhibited the lowest binding energy with oleic acid (−6.5 kcal/mol) among the highly expressed FAD2 proteins. Heterologous expression in yeast confirmed that PgFAD2-56 altered fatty acid composition by producing linoleic acid and enhanced cold stress resistance. Conclusion This study demonstrates that the ginseng FAD gene family exhibits strong subfamily specificity and plays a vital role in stress resistance, with the expansion of the FAD2 subfamily and functional characterization of PgFAD2-56 providing potential targets for stress-resistant molecular breeding in P. ginseng., authors=SONG Xiaoli, ZHU Yuanchun, YANG Guishu, ZHANG Wei, JIANG Haiyan, XI Yang, HUANG Qin, YANG Qiong, HU Xueping, authorsList=SONG Xiaoli, ZHU Yuanchun, YANG Guishu, ZHANG Wei, JIANG Haiyan, XI Yang, HUANG Qin, YANG Qiong, HU Xueping, authorCompany=null, correspAuthors=null, 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=1304388208125567595, articleId=1304388207668388458, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=基于T2T基因组的人参FAD基因家族鉴定及PgFAD2-56的功能验证, columnId=1304140203967410414, journalTitle=中草药, columnName=药材与资源, runingTitle=null, highlight=null, articleAbstract=目的 旨在系统鉴定人参FAD基因(Panax ginseng FADPgFAD)家族并验证PgFAD2-56的功能,以期揭示PgFAD基因的功能和胁迫响应机制。方法 利用生物信息学手段从人参T2T基因组中鉴定PgFAD基因家族成员,分析其理化性质、系统进化、染色体定位、基因结构、保守基序、顺式作用元件及共线性特征,以及胁迫条件下的表达模式;通过分子对接预测高表达FAD2与油酸的结合能力;以酿酒酵母作为异源表达底盘验证PgFAD2-56的功能。结果 从人参T2T基因组中共鉴定到98个PgFAD基因,根据氨基酸序列相似性可分为6个亚家族(ADSSLDFAD3/FAD7/FAD8FAD6FAD2FAB),这种分类得到基因结构和保守基序的支持。启动子区鉴定出大量激素和应激响应顺式作用元件及转录因子结合位点(TFBS),表明PgFADs的表达调控受到多种因素影响。共线性分析发现FAD2亚族在人参中具有显著扩张。基因表达分析发现部分PgFADs在胁迫响应中呈显著差异表达。分子对接结果显示FAD2-56与油酸的结合能最低(−6.5 kcal/mol),底物偏好性优于其他高表达FAD2基因。酵母异源表达实验证实PgFAD2-56可改变脂肪酸组分,使转基因酵母产生亚油酸,并增强其对寒冷胁迫的抗性。结论 PgFAD基因家族具有强烈的亚族特异性,在人参抗逆中发挥着重要作用,FAD2亚族的扩张及PgFAD2-56的功能验证为人参抗逆分子育种提供了潜在靶点。, authors=宋晓丽1, 祝元春1,2, 杨贵舒3, 张伟4, 蒋海艳1, 席杨1, 黄芹1, 杨琼1, 胡雪萍2, authorsList=宋晓丽, 祝元春, 杨贵舒, 张伟, 蒋海艳, 席杨, 黄芹, 杨琼, 胡雪萍, authorCompany=1 重庆市中林峰科技发展有限公司,重庆 401121;
2 重庆市林业科学研究院,重庆 401121;
3 重庆森威林业发展有限公司,重庆 404100;
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Jayakodi M, Choi B S, Lee S C, et al. Ginseng Genome Database: An open-access platform for genomics of Panax ginseng [J]. BMC Plant Biol, 2018, 18(1): 62.
Huang X, Zhou Y, Shi X, et al. PfbZIP85 transcription factor mediates ω-3 fatty acid-enriched oil biosynthesis by down-regulating PfLPAT1B gene expression in plant tissues [J]. Internat J Mol Sci, 2024, 25(8): 4375.
孙婷婷, 刘瑞鹏, 杜鹏禹, 等. 过表达平菇MADS-box转录因子提高酿酒酵母多种胁迫耐受性[J]. 食品科技, 2025, 50(5): 18-26.
Wei H, Movahedi A, Xu S Z, et al. Genome-wide characterization and expression analysis of fatty acid desaturase gene family in poplar [J]. Int J Mol Sci, 2022, 23: (19):11109.
Hajiahmadi Z, Abedi A, Wei H, et al. Identification, evolution, expression, and docking studies of fatty acid desaturase genes in wheat (Triticum aestivum L.) [J]. BMC Genom, 2020, 21(1): 778.
E Z G, Chen C, Yang J Y, et al. Genome-wide analysis of fatty acid desaturase genes in rice (Oryza sativa L.) [J]. Sci Rep, 2019, 9: 19445.
Johnson D A, Thomas M A. The monosaccharide transporter gene family in Arabidopsis and rice: A history of duplications, adaptive evolution, and functional divergence [J]. Mol Biol Evol, 2007, 24(11): 2412-2423.
张明亚, 庞胜群, 刘玉东, 等. 番茄FAD基因家族的鉴定与表达分析[J]. 生物技术通报, 2024, 40(7): 150-162.
侯静静, 赵利, 王斌. 亚麻FAD基因家族的生物信息学鉴定分析[J]. 寒旱农业科学, 2023, 2(3): 246-253.
Li J, Wang Q, Han C, et al. Transcriptional analysis of different cultivars and genome-wide identification of FAD gene family in tree peony [J]. Agronomy, 2024, 14(10): 2378.
Peng Z Y, Ruan J, Tian H Y, et al. The family of peanut fatty acid desaturase genes and a functional analysis of four ω-3 AhFAD3 members [J]. Plant Mol Biol Report, 2020, 38(2): 209-221.
Rzhetsky A, Hsu L C, et al. Exon/intron structure of aldehyde dehydrogenase genes supports the “introns-late” theory [J]. Proc Natl Acad Sci U S A, 1997, 94(13): 6820-6825.
Xu L, Zeng W J, Li J J, et al. Characteristics of membrane-bound fatty acid desaturase (FAD) genes in Brassica napus L. and their expressions under different cadmium and salinity stresses [J]. Environ Exp Bot, 2019, 162: 144-156.
Ohlrogge J, Browse J. Lipid biosynthesis [J]. The Plant Cell, 1995, 7(7): 957-970.
Li R, Zhu F, Duan D. Function analysis and stress-mediated cis -element identification in the promoter region of VqMYB15[J]. Plant Signaling & Behavior, 2020, 15(7): 1773664.
Murphy D J, Stumpf P K. Light-dependent induction of polyunsaturated fatty acid biosynthesis in greening cucumber cotyledons [J]. Plant Physiol, 1979, 63(2): 328-335.
Dar A A, Choudhury A R, Kancharla P K, et al. The FAD2 gene in plants: occurrence, regulation, and role [J]. Front Plant Sci, 2017, 8: 1789.)
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基于T2T基因组的人参FAD基因家族鉴定及PgFAD2-56的功能验证
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中草药 | 药材与资源 2026,57(12): 4811-4822
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中草药 |药材与资源 2026 , 57 (12) : 4811 -4822
基于T2T基因组的人参FAD基因家族鉴定及PgFAD2-56的功能验证
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宋晓丽1, 祝元春1,2, 杨贵舒3, 张伟4, 蒋海艳1, 席杨1, 黄芹1, 杨琼1, 胡雪萍2
作者信息
    1 重庆市中林峰科技发展有限公司,重庆 401121;
    2 重庆市林业科学研究院,重庆 401121;
    3 重庆森威林业发展有限公司,重庆 404100;
    4 参仙源参业股份有限公司,辽宁 沈阳 118200
通讯作者:
祝元春
作者简介:
宋晓丽: 宋晓丽(1988—),女,工程师,从事林下中药材开发、新品种培育、绿色生态种植技术等研究。E-mail:984848819@qq.com
Identification of Panax ginseng FAD gene family based on T2T genome and functional verification of PgFAD2-56
  • SONG Xiaoli, ZHU Yuanchun, YANG Guishu, ZHANG Wei, JIANG Haiyan, XI Yang, HUANG Qin, YANG Qiong, HU Xueping
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.12.023
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    目的 旨在系统鉴定人参FAD基因(Panax ginseng FADPgFAD)家族并验证PgFAD2-56的功能,以期揭示PgFAD基因的功能和胁迫响应机制。方法 利用生物信息学手段从人参T2T基因组中鉴定PgFAD基因家族成员,分析其理化性质、系统进化、染色体定位、基因结构、保守基序、顺式作用元件及共线性特征,以及胁迫条件下的表达模式;通过分子对接预测高表达FAD2与油酸的结合能力;以酿酒酵母作为异源表达底盘验证PgFAD2-56的功能。结果 从人参T2T基因组中共鉴定到98个PgFAD基因,根据氨基酸序列相似性可分为6个亚家族(ADSSLDFAD3/FAD7/FAD8FAD6FAD2FAB),这种分类得到基因结构和保守基序的支持。启动子区鉴定出大量激素和应激响应顺式作用元件及转录因子结合位点(TFBS),表明PgFADs的表达调控受到多种因素影响。共线性分析发现FAD2亚族在人参中具有显著扩张。基因表达分析发现部分PgFADs在胁迫响应中呈显著差异表达。分子对接结果显示FAD2-56与油酸的结合能最低(−6.5 kcal/mol),底物偏好性优于其他高表达FAD2基因。酵母异源表达实验证实PgFAD2-56可改变脂肪酸组分,使转基因酵母产生亚油酸,并增强其对寒冷胁迫的抗性。结论 PgFAD基因家族具有强烈的亚族特异性,在人参抗逆中发挥着重要作用,FAD2亚族的扩张及PgFAD2-56的功能验证为人参抗逆分子育种提供了潜在靶点。
    人参  /  全基因组鉴定  /  FAD基因家族  /  不饱和脂肪酸  /  生物信息学分析
    Objective FAD enzymes introduce double bonds at specific positions in fatty acids, converting saturated fatty acids into unsaturated fatty acids, playing crucial roles in plant growth, development, and stress responses. This study aimed to systematically identify the FAD gene family in Panax ginseng and verify the function of PgFAD2-56, so as to elucidate the functions and stress response mechanisms of ginseng FAD genes. Methods Using bioinformatics approaches, 98 PgFAD genes were identified from the P. ginseng T2T genome, and their physicochemical properties, phylogenetic relationships, chromosomal localization, gene structures, conserved motifs, cis-acting regulatory elements, collinearity, and expression patterns under stress conditions were analyzed. Molecular docking was performed to predict the binding affinity of highly expressed FAD2 proteins with oleic acid, and the function of PgFAD2-56 was verified using a yeast heterologous expression system. Results The results showed that the 98 PgFAD genes could be classified into six subfamilies (ADS, SLD, FAD3/FAD7/FAD8, FAD6, FAD2, and FAB) based on amino acid sequence similarity, which was consistently supported by their gene structures and conserved motifs. Numerous hormone- and stress-responsive cis-acting elements and transcription factor binding sites (TFBSs) were identified in the promoters of PgFAD genes. Collinearity analysis revealed significant expansion of the FAD2 subfamily in P. ginseng. Gene expression analysis demonstrated that some PgFADs displayed significant differential expression under stress conditions. Molecular docking indicated that FAD2-56 exhibited the lowest binding energy with oleic acid (−6.5 kcal/mol) among the highly expressed FAD2 proteins. Heterologous expression in yeast confirmed that PgFAD2-56 altered fatty acid composition by producing linoleic acid and enhanced cold stress resistance. Conclusion This study demonstrates that the ginseng FAD gene family exhibits strong subfamily specificity and plays a vital role in stress resistance, with the expansion of the FAD2 subfamily and functional characterization of PgFAD2-56 providing potential targets for stress-resistant molecular breeding in P. ginseng.
    Panax ginseng C. A. Mey.  /  whole genome identification  /  FAD gene family  /  unsaturated fatty acids  /  bioinformatics analysis
    宋晓丽, 祝元春, 杨贵舒, 张伟, 蒋海艳, 席杨, 黄芹, 杨琼, 胡雪萍. 基于T2T基因组的人参FAD基因家族鉴定及PgFAD2-56的功能验证. 中草药, 2026 , 57 (12) : 4811 -4822 . DOI: 10.7501/j.issn.0253-2670.2026.12.023
    SONG Xiaoli, ZHU Yuanchun, YANG Guishu, ZHANG Wei, JIANG Haiyan, XI Yang, HUANG Qin, YANG Qiong, HU Xueping. Identification of Panax ginseng FAD gene family based on T2T genome and functional verification of PgFAD2-56[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (12) : 4811 -4822 . DOI: 10.7501/j.issn.0253-2670.2026.12.023

      中国农业产业发展基金 (1260233)

    参考文献 引证文献
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    Chen C J, Wu Y, Li J W, et al. TBtools-II: A “one for all, all for one” bioinformatics platform for biological big-data mining [J]. Mol Plant, 2023, 16(11): 1733-1742.
    Jayakodi M, Choi B S, Lee S C, et al. Ginseng Genome Database: An open-access platform for genomics of Panax ginseng [J]. BMC Plant Biol, 2018, 18(1): 62.
    Huang X, Zhou Y, Shi X, et al. PfbZIP85 transcription factor mediates ω-3 fatty acid-enriched oil biosynthesis by down-regulating PfLPAT1B gene expression in plant tissues [J]. Internat J Mol Sci, 2024, 25(8): 4375.
    孙婷婷, 刘瑞鹏, 杜鹏禹, 等. 过表达平菇MADS-box转录因子提高酿酒酵母多种胁迫耐受性[J]. 食品科技, 2025, 50(5): 18-26.
    Wei H, Movahedi A, Xu S Z, et al. Genome-wide characterization and expression analysis of fatty acid desaturase gene family in poplar [J]. Int J Mol Sci, 2022, 23: (19):11109.
    Hajiahmadi Z, Abedi A, Wei H, et al. Identification, evolution, expression, and docking studies of fatty acid desaturase genes in wheat (Triticum aestivum L.) [J]. BMC Genom, 2020, 21(1): 778.
    E Z G, Chen C, Yang J Y, et al. Genome-wide analysis of fatty acid desaturase genes in rice (Oryza sativa L.) [J]. Sci Rep, 2019, 9: 19445.
    Johnson D A, Thomas M A. The monosaccharide transporter gene family in Arabidopsis and rice: A history of duplications, adaptive evolution, and functional divergence [J]. Mol Biol Evol, 2007, 24(11): 2412-2423.
    张明亚, 庞胜群, 刘玉东, 等. 番茄FAD基因家族的鉴定与表达分析[J]. 生物技术通报, 2024, 40(7): 150-162.
    侯静静, 赵利, 王斌. 亚麻FAD基因家族的生物信息学鉴定分析[J]. 寒旱农业科学, 2023, 2(3): 246-253.
    Li J, Wang Q, Han C, et al. Transcriptional analysis of different cultivars and genome-wide identification of FAD gene family in tree peony [J]. Agronomy, 2024, 14(10): 2378.
    Peng Z Y, Ruan J, Tian H Y, et al. The family of peanut fatty acid desaturase genes and a functional analysis of four ω-3 AhFAD3 members [J]. Plant Mol Biol Report, 2020, 38(2): 209-221.
    Rzhetsky A, Hsu L C, et al. Exon/intron structure of aldehyde dehydrogenase genes supports the “introns-late” theory [J]. Proc Natl Acad Sci U S A, 1997, 94(13): 6820-6825.
    Xu L, Zeng W J, Li J J, et al. Characteristics of membrane-bound fatty acid desaturase (FAD) genes in Brassica napus L. and their expressions under different cadmium and salinity stresses [J]. Environ Exp Bot, 2019, 162: 144-156.
    Ohlrogge J, Browse J. Lipid biosynthesis [J]. The Plant Cell, 1995, 7(7): 957-970.
    Li R, Zhu F, Duan D. Function analysis and stress-mediated cis -element identification in the promoter region of VqMYB15[J]. Plant Signaling & Behavior, 2020, 15(7): 1773664.
    Murphy D J, Stumpf P K. Light-dependent induction of polyunsaturated fatty acid biosynthesis in greening cucumber cotyledons [J]. Plant Physiol, 1979, 63(2): 328-335.
    Dar A A, Choudhury A R, Kancharla P K, et al. The FAD2 gene in plants: occurrence, regulation, and role [J]. Front Plant Sci, 2017, 8: 1789.
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    doi: 10.7501/j.issn.0253-2670.2026.12.023
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    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
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    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
    小菇属 Mycena 11 5.26
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