Article(id=1304406884820218029, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.01.023, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1757001600000, receivedDateStr=2025-09-05, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924436048, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924436048, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924436048, creator=13701087609, updateTime=1788924436048, updator=13701087609, issue=Issue{id=1304406818550206926, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='1', pageStart='1', pageEnd='389', issueExtLink='null', onlineDate='null', pubDate='1768147200000', pubDateStr='2026-01-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924420249, creator='13701087609', updateTime=1788924674802, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407886289986387, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407886289986388, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=256, endPage=269, ext={EN=ArticleExt(id=1304406887231942832, articleId=1304406884820218029, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Genome wide identification of Coptis chinensis P450 gene family and evolutionary specificity of CYP719 genes, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To mine CYP gene family members in Coptis chinensis based on genomic data and analyze the evolutionary specificity of CYP719 genes. Methods The CYP gene family members of C. chinensis were identified based on homologous CYP gene sequence from both Arabidopsis thaliana and Oryza sativa. Analyses of the physicochemical properties of proteins, system classification, gene structure, expression profile and cis-acting elements of the identified CYP genes were further conducted by bioinformatics. The CYP719 family members in C. chinensis were identified based on the 23 reported CYP719 genes in other plants, and their collinearity analysis was performed through homologous sequence alignment. Results A total of 308 CYP genes were identified in the C. chinensis genomic data, belonging to 45 families in nine family clans. The range of amino acid numbers for encoded proteins is from 103 to 2 008 aa, with a relative molecular mass ranging from 11 010 to 230 370, and an isoelectric point ranging from 4.85 to 9.79. The number of CYP gene exons in C. chinensis varies between 1 and 38, with a wide range of variation. A total of 308 CYP genes were unevenly distributed on nine chromosomes of C. chinensis and mainly expanded through dispersed duplication(DSD) and proximal duplication(PD). The expression of CYP genes was tissue-specific, and nine genes were significantly upregulated in rhizomes and fibrous roots. In the promoter regions of these CYP genes, stress response elements were predicted to be the most frequently occurring cis-acting elements. Through genomic collinear analyses between different plants, the C. chinensis CYP719 genes have homologous ones in Aquilegia coerulea, Corydalis tomentella, Papaver somniferum, and Aristolochia debilis, but not in Arabidopsis thaliana, Glycine max, Prunus persica, Chrysanthemum nankingense, Vitis vinifera, Aconitum vilmorinianum, O. sativa, and Amborella trichopoda. Conclusion C. chinensis has a rich CYP supergene family, in which CYP719 gene shows branch-specific evolution, laying the foundation for analyzing the functions of this type of gene., authors=WANG Yuting, LI Guofeng, TAO Qi, LIU Di, PEI Liuling, LIU Yifei, authorsList=WANG Yuting, LI Guofeng, TAO Qi, LIU Di, PEI Liuling, LIU Yifei, 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=1304406886980284591, articleId=1304406884820218029, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=黄连P450基因家族全基因组鉴定及CYP719基因的进化特异性分析, columnId=1304140203967410414, journalTitle=中草药, columnName=药材与资源, runingTitle=null, highlight=null, articleAbstract=目的 基于基因组数据挖掘黄连Coptis chinensis细胞色素P450(Cytochrome P450,CYP)基因家族成员,并分析黄连CYP719基因的进化特异性。方法 基于拟南芥Arabidopsis thaliana和水稻Oryza sativaCYP基因序列鉴定黄连CYP基因家族成员,利用生物信息学对黄连CYP基因家族成员进行蛋白理化性质、系统分类、基因结构、表达图谱和顺式作用元件等分析;基于23条已报道的CYP719基因鉴定黄连中CYP719家族成员,基于同源序列比对进行共线性分析。结果 在黄连基因组数据中共鉴定得到308个CYP基因,归属9个家族簇的45个家族。编码蛋白的氨基酸数量分布在103~2 008 aa,相对分子质量介于11 010~230 370,等电点介于4.85~9.79。黄连CYP基因外显子数量范围为1~38个,变化范围较大。308个黄连CYP基因不均一地分布在9条染色体上,主要通过分散复制(dispersed duplication,DSD)和邻近复制(proximal duplication,PD)进行扩张。CYP基因表达具有组织特异性,有9个基因在根茎和须根中表达显著上调。胁迫响应元件是黄连CYP基因启动子区预测最多的顺式作用元件。比较基因组分析表明,CYP719基因在耧斗菜、毛黄堇、罂粟和马兜铃中有分布,在拟南芥、大豆、桃、菊花脑、葡萄、黄草乌、水稻和无油樟中均没有同源基因。结论 黄连中拥有丰富的CYP超基因家族,且CYP719基因呈现支系特异性进化,为解析该类基因的功能奠定基础。, authors=王雨婷1, 李国凤1, 陶琦1, 刘迪1, 裴柳玲1,2, 刘义飞1,2, authorsList=王雨婷, 李国凤, 陶琦, 刘迪, 裴柳玲, 刘义飞, authorCompany=1 湖北中医药大学药学院, 湖北 武汉 430065;
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Ikezawa N, Tanaka M, Nagayoshi M, et al. Molecular cloning and characterization of CYP719, a methylenedioxy bridge-forming enzyme that belongs to a novel P450 family, from cultured Coptis japonica cells[J]. J Biol Chem, 2003, 278(40):38557-38565.
Ikezawa N, Iwasa K, Sato F. Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of(S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells[J]. J Biol Chem, 2008, 283(14):8810-8821.
Tian Y, Kong L Z, Li Q, et al. Structural diversity,evolutionary origin, and metabolic engineering of plant specialized benzylisoquinoline alkaloids[J]. Nat Prod Rep, 2024, 41(11):1787-1810.
Gesell A, Rolf M, Ziegler J, et al. CYP719B1 is salutaridine synthase, the C-C phenol-coupling enzyme of morphine biosynthesis in opium poppy[J]. J Biol Chem,2009, 284(36):24432-24442.
Mizutani M, Sato F. Unusual P450 reactions in plant secondary metabolism[J]. Arch Biochem Biophys, 2011,507(1):194-203.
Ikezawa N, Iwasa K, Sato F. CYP719A subfamily of cytochrome P450 oxygenases and isoquinoline alkaloid biosynthesis in Eschscholzia californica[J]. Plant Cell Rep, 2009, 28(1):123-133.
Chávez M L D, Rolf M, Gesell A, et al. Characterization of two methylenedioxy bridge-forming cytochrome P450-dependent enzymes of alkaloid formation in the Mexican prickly poppy Argemone mexicana[J]. Arch Biochem Biophys, 2011, 507(1):186-193.
Liu X Y, Jiao X, Cheng Y T, et al. Structure-function analysis of CYP719As involved in methylenedioxy bridge-formation in the biosynthesis of benzylisoquinoline alkaloids and its de novo production[J]. Microb Cell Fact,2023, 22(1):23.
Schnabel A, Cotinguiba F, Athmer B, et al. Piper nigrum CYP719A37 catalyzes the decisive methylenedioxy bridge formation in piperine biosynthesis[J]. Plants, 2021,10(1):128.
赵力.莲叶片生物碱合成基因的挖掘及功能鉴定[D]. 福州:福建农林大学, 2019.
Nelson D R, Schuler M A. Cytochrome P450 genes from the sacred Lotus genome[J]. Trop Plant Biol, 2013, 6(2):138-151.
Liu Y F, Wang B, Shu S H, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids[J]. Nat Commun, 2021, 12(1):3276.
Wu L, Zhao B, Deng Z, et al. A biosynthetic network for protoberberine production in Coptis chinensis[J]. Hortic Res, 2024, 11(1):uhad259.
Chen C J, Chen H, Zhang Y, et al. TBtools:An integrative toolkit developed for interactive analyses of big biological data[J]. Mol Plant, 2020, 13(8):1194-1202.
Nelson D R, Koymans L, Kamataki T, et al. P450superfamily:Update on new sequences, gene mapping,accession numbers and nomenclature[J]. Pharmacogenetics, 1996, 6(1):1-42.
李翔宇,王助乾,孙春玉,等.植物细胞色素P450s及其在植物新陈代谢中的作用[J]. 安徽农业科学, 2016,44(13):129-134.
宋展,高鑫,吴冕,等.细胞色素P450酶的结构、功能与应用研究进展[J]. 微生物学通报, 2020, 47(7):2245-2254.
Xu G X, Guo C C, Shan H Y, et al. Divergence of duplicate genes in exon-intron structure[J]. Proc Natl Acad Sci USA,2012, 109(4):1187-1192.
李彩虹,周克元.黄连活性成分的作用及机制研究进展[J]. 时珍国医国药, 2010, 21(2):466-468.
Jin X Y, Liu Y H, Hou Z M, et al. Genome-wide investigation of SBT family genes in pineapple and functional analysis of AcoSBT1.12 in floral transition[J]. Front Genet, 2021, 12:730821.
盖晓红,刘素香,任涛,等.黄连的化学成分及药理作用研究进展[J]. 中草药, 2018, 49(20):4919-4927.
李淑萍,陈丽,贺飞,等.基于HPLC指纹图谱和6种指标成分的经典名方黄连膏基准样品量值传递分析[J]. 中草药, 2025, 56(17):6196-6206.
赵楠,李隆云,白志川.中药材黄连的研究现状与展望[J]. 重庆理工大学学报:自然科学, 2015, 29(1):53-58.
Nelson D, Werck-Reichhart D. A P450-centric view of plant evolution[J]. Plant J, 2011, 66(1):194-211.
Jiu S T, Xu Y, Wang J Y, et al. The cytochrome P450monooxygenase inventory of grapevine(Vitis vinifera L.):Genome-wide identification, evolutionary characterization and expression analysis[J]. Front Genet, 2020, 11:44.
Lin X J, Tang B Q, Li Z Q, et al. Genome-wide identification and expression analyses of CYP450 genes in sweet potato(Ipomoea batatas L.)[J]. BMC Genomics,2024, 25(1):58.
Wei K F, Chen H Q. Global identification, structural analysis and expression characterization of cytochrome P450 monooxygenase superfamily in rice[J]. BMC Genomics, 2018, 19(1):35.
Khatri P, Wally O, Rajcan I, et al. Comprehensive analysis of cytochrome P450 monooxygenases reveals insight into their role in partial resistance against Phytophthora sojae in soybean[J]. Front Plant Sci, 2022, 13:862314.
Hansen C C, Nelson D R, Møller B L, et al. Plant cytochrome P450 plasticity and evolution[J]. Mol Plant,2021, 14(8):1244-1265.
Manikandan P, Nagini S. Cytochrome P450 structure,function and clinical significance:A review[J]. Curr Drug Targets, 2018, 19(1):38-54.
Xu J, Wang X Y, Guo W Z. The cytochrome P450superfamily:Key players in plant development and defense[J]. J Integr Agric, 2015, 14(9):1673-1686.
Pandian B A, Sathishraj R, Djanaguiraman M, et al. Role of cytochrome P450 enzymes in plant stress response[J]. Antioxidants, 2020, 9(5):454.
刘微,刘义飞,陈士林,等.茉莉酸甲酯对黄连生物碱含量积累的影响[J]. 世界中医药, 2022, 17(13):1813-1818.)
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黄连P450基因家族全基因组鉴定及CYP719基因的进化特异性分析
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中草药 |药材与资源 2026 , 57 (1) : 256 -269
黄连P450基因家族全基因组鉴定及CYP719基因的进化特异性分析
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王雨婷1, 李国凤1, 陶琦1, 刘迪1, 裴柳玲1,2, 刘义飞1,2
作者信息
    1 湖北中医药大学药学院, 湖北 武汉 430065;
    2 湖北时珍实验室, 湖北 武汉 430061
通讯作者:
裴柳玲
作者简介:
王雨婷: 王雨婷(2000-),女,硕士研究生,研究方向为中药资源品质评价及开发利用。E-mail:1660662082@qq.com
Genome wide identification of Coptis chinensis P450 gene family and evolutionary specificity of CYP719 genes
  • WANG Yuting, LI Guofeng, TAO Qi, LIU Di, PEI Liuling, LIU Yifei
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.01.023
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    目的 基于基因组数据挖掘黄连Coptis chinensis细胞色素P450(Cytochrome P450,CYP)基因家族成员,并分析黄连CYP719基因的进化特异性。方法 基于拟南芥Arabidopsis thaliana和水稻Oryza sativaCYP基因序列鉴定黄连CYP基因家族成员,利用生物信息学对黄连CYP基因家族成员进行蛋白理化性质、系统分类、基因结构、表达图谱和顺式作用元件等分析;基于23条已报道的CYP719基因鉴定黄连中CYP719家族成员,基于同源序列比对进行共线性分析。结果 在黄连基因组数据中共鉴定得到308个CYP基因,归属9个家族簇的45个家族。编码蛋白的氨基酸数量分布在103~2 008 aa,相对分子质量介于11 010~230 370,等电点介于4.85~9.79。黄连CYP基因外显子数量范围为1~38个,变化范围较大。308个黄连CYP基因不均一地分布在9条染色体上,主要通过分散复制(dispersed duplication,DSD)和邻近复制(proximal duplication,PD)进行扩张。CYP基因表达具有组织特异性,有9个基因在根茎和须根中表达显著上调。胁迫响应元件是黄连CYP基因启动子区预测最多的顺式作用元件。比较基因组分析表明,CYP719基因在耧斗菜、毛黄堇、罂粟和马兜铃中有分布,在拟南芥、大豆、桃、菊花脑、葡萄、黄草乌、水稻和无油樟中均没有同源基因。结论 黄连中拥有丰富的CYP超基因家族,且CYP719基因呈现支系特异性进化,为解析该类基因的功能奠定基础。
    黄连  /  细胞色素P450  /  生物信息学分析  /  表达模式  /  分散复制  /  邻近复制
    Objective To mine CYP gene family members in Coptis chinensis based on genomic data and analyze the evolutionary specificity of CYP719 genes. Methods The CYP gene family members of C. chinensis were identified based on homologous CYP gene sequence from both Arabidopsis thaliana and Oryza sativa. Analyses of the physicochemical properties of proteins, system classification, gene structure, expression profile and cis-acting elements of the identified CYP genes were further conducted by bioinformatics. The CYP719 family members in C. chinensis were identified based on the 23 reported CYP719 genes in other plants, and their collinearity analysis was performed through homologous sequence alignment. Results A total of 308 CYP genes were identified in the C. chinensis genomic data, belonging to 45 families in nine family clans. The range of amino acid numbers for encoded proteins is from 103 to 2 008 aa, with a relative molecular mass ranging from 11 010 to 230 370, and an isoelectric point ranging from 4.85 to 9.79. The number of CYP gene exons in C. chinensis varies between 1 and 38, with a wide range of variation. A total of 308 CYP genes were unevenly distributed on nine chromosomes of C. chinensis and mainly expanded through dispersed duplication(DSD) and proximal duplication(PD). The expression of CYP genes was tissue-specific, and nine genes were significantly upregulated in rhizomes and fibrous roots. In the promoter regions of these CYP genes, stress response elements were predicted to be the most frequently occurring cis-acting elements. Through genomic collinear analyses between different plants, the C. chinensis CYP719 genes have homologous ones in Aquilegia coerulea, Corydalis tomentella, Papaver somniferum, and Aristolochia debilis, but not in Arabidopsis thaliana, Glycine max, Prunus persica, Chrysanthemum nankingense, Vitis vinifera, Aconitum vilmorinianum, O. sativa, and Amborella trichopoda. Conclusion C. chinensis has a rich CYP supergene family, in which CYP719 gene shows branch-specific evolution, laying the foundation for analyzing the functions of this type of gene.
    Coptis chinensis Franch.  /  cytochrome P450  /  bioinformatics analysis  /  expression analysis  /  dispersed duplication  /  proximal duplication
    王雨婷, 李国凤, 陶琦, 刘迪, 裴柳玲, 刘义飞. 黄连P450基因家族全基因组鉴定及CYP719基因的进化特异性分析. 中草药, 2026 , 57 (1) : 256 -269 . DOI: 10.7501/j.issn.0253-2670.2026.01.023
    WANG Yuting, LI Guofeng, TAO Qi, LIU Di, PEI Liuling, LIU Yifei. Genome wide identification of Coptis chinensis P450 gene family and evolutionary specificity of CYP719 genes[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (1) : 256 -269 . DOI: 10.7501/j.issn.0253-2670.2026.01.023

      国家自然科学基金项目 (32270231); 湖北时珍实验室首席科学家项目 (HSL2024SX0006)

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    Ikezawa N, Iwasa K, Sato F. Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of(S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells[J]. J Biol Chem, 2008, 283(14):8810-8821.
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    Ikezawa N, Iwasa K, Sato F. CYP719A subfamily of cytochrome P450 oxygenases and isoquinoline alkaloid biosynthesis in Eschscholzia californica[J]. Plant Cell Rep, 2009, 28(1):123-133.
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    Schnabel A, Cotinguiba F, Athmer B, et al. Piper nigrum CYP719A37 catalyzes the decisive methylenedioxy bridge formation in piperine biosynthesis[J]. Plants, 2021,10(1):128.
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    Nelson D R, Schuler M A. Cytochrome P450 genes from the sacred Lotus genome[J]. Trop Plant Biol, 2013, 6(2):138-151.
    Liu Y F, Wang B, Shu S H, et al. Analysis of the Coptis chinensis genome reveals the diversification of protoberberine-type alkaloids[J]. Nat Commun, 2021, 12(1):3276.
    Wu L, Zhao B, Deng Z, et al. A biosynthetic network for protoberberine production in Coptis chinensis[J]. Hortic Res, 2024, 11(1):uhad259.
    Chen C J, Chen H, Zhang Y, et al. TBtools:An integrative toolkit developed for interactive analyses of big biological data[J]. Mol Plant, 2020, 13(8):1194-1202.
    Nelson D R, Koymans L, Kamataki T, et al. P450superfamily:Update on new sequences, gene mapping,accession numbers and nomenclature[J]. Pharmacogenetics, 1996, 6(1):1-42.
    李翔宇,王助乾,孙春玉,等.植物细胞色素P450s及其在植物新陈代谢中的作用[J]. 安徽农业科学, 2016,44(13):129-134.
    宋展,高鑫,吴冕,等.细胞色素P450酶的结构、功能与应用研究进展[J]. 微生物学通报, 2020, 47(7):2245-2254.
    Xu G X, Guo C C, Shan H Y, et al. Divergence of duplicate genes in exon-intron structure[J]. Proc Natl Acad Sci USA,2012, 109(4):1187-1192.
    李彩虹,周克元.黄连活性成分的作用及机制研究进展[J]. 时珍国医国药, 2010, 21(2):466-468.
    Jin X Y, Liu Y H, Hou Z M, et al. Genome-wide investigation of SBT family genes in pineapple and functional analysis of AcoSBT1.12 in floral transition[J]. Front Genet, 2021, 12:730821.
    盖晓红,刘素香,任涛,等.黄连的化学成分及药理作用研究进展[J]. 中草药, 2018, 49(20):4919-4927.
    李淑萍,陈丽,贺飞,等.基于HPLC指纹图谱和6种指标成分的经典名方黄连膏基准样品量值传递分析[J]. 中草药, 2025, 56(17):6196-6206.
    赵楠,李隆云,白志川.中药材黄连的研究现状与展望[J]. 重庆理工大学学报:自然科学, 2015, 29(1):53-58.
    Nelson D, Werck-Reichhart D. A P450-centric view of plant evolution[J]. Plant J, 2011, 66(1):194-211.
    Jiu S T, Xu Y, Wang J Y, et al. The cytochrome P450monooxygenase inventory of grapevine(Vitis vinifera L.):Genome-wide identification, evolutionary characterization and expression analysis[J]. Front Genet, 2020, 11:44.
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    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
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    红菇属 Russula 17 8.13
    栓菌属 Trametes 5 2.39
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