Article(id=1304388085345705991, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388047747969563, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.10.022, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1767369600000, receivedDateStr=2026-01-03, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919953905, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919953905, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919953904, creator=13701087609, updateTime=1788919953904, updator=13701087609, issue=Issue{id=1304388047747969563, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='10', pageStart='3685', pageEnd='4088', issueExtLink='null', onlineDate='null', pubDate='1779897600000', pubDateStr='2026-05-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919944940, creator='13701087609', updateTime=1788923403989, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402556332037104, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388047747969563, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402556332037105, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388047747969563, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=3940, endPage=3953, ext={EN=ArticleExt(id=1304388087350583305, articleId=1304388085345705991, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Identification and expression analysis of WRKY transcription factor family in Codonopsis pilosula, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To identify members of the WRKY transcription factor family in Codonopsis pilosula at the genome-wide level and analyze their characteristics, and explore their potential roles in response to salt stress, thereby laying a foundation for functional studies of C. pilosula WRKY transcription factors. Methods Potential gene family members were screened across the entire genome based on conserved protein domains using the Hidden Markov model (HMM). Protein sequence alignment, conserved domain analysis, phylogenetic tree construction, gene synteny analysis, and cis-acting element analysis in the promoter region were performed using software and online tools including MAFFT, IQ-TREE, MEME, Plant CARE and TBtools. Expression patterns of WRKY genes were analyzed based on transcriptome data from different tissues (roots, stems, leaves, and flowers) and qRT-PCR was used to determine their relative expression levels. In addition, the transcriptome data of C. pilosula treated with 0, 60, and 120 mmol/L NaCl were analyzed to examine the expression changes of WRKY genes under salt stress. Results A total of 50 WRKY transcription factor members were identified in C. pilosula. Motif analysis showed that all members contained the typical WRKY domain with the conserved sequence WRKYGQK. Phylogenetic analysis with WRKY transcription factors from Arabidopsis thaliana and Oryza sativa classified the 50 C. pilosula WRKY transcription factors into three groups, with group II further divided into five subgroups. The amino acid lengths of the identified WRKY proteins ranged from 103 to 986 residues, with isoelectric points (pI) of 4.87−9.99 and molecular weights (MW) of 12 435.14−107 946.28. Gene expression analysis revealed significant differences in the expression levels of CpWRKY26, CpWRKY48, CpWRKY2, and CpWRKY49 among roots, stems, leaves, and flowers of C. pilosula. The results of salt stress treatment indicated that most CpWRKY genes showed differential expression trends under different concentrations of NaCl, and some members cluster phylogenetically with previously reported salt-tolerant WRKY genes, suggesting that they may be involved in the regulation of C. pilosula salt stress responses. Conclusion This study represents the first systematic identification and bioinformatics analysis of the WRKY gene family in C. pilosula at the genome-wide level. By combining tissue expression and salt stress response analyses, the study reveales that the WRKY genes in C. pilosula may be involved in physiological processes such as growth and development, secondary metabolite biosynthesis, and stress responses. This lays a theoretical foundation for further research on the functions of WRKY genes and their roles in regulating medicinal components, and provides gene resources and scientific evidence for molecular-assisted breeding of C. pilosula., authors=WANG Chunhui, SONG Min, FAN Panhui, WAN Huihua, WANG Feifei, SUN Wei, CAO Xue, MA Jing, authorsList=WANG Chunhui, SONG Min, FAN Panhui, WAN Huihua, WANG Feifei, SUN Wei, CAO Xue, MA Jing, 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=1304388087279280136, articleId=1304388085345705991, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=党参中WRKY转录因子家族的鉴定及表达分析, columnId=1304140203967410414, journalTitle=中草药, columnName=药材与资源, runingTitle=null, highlight=null, articleAbstract=目的 在全基因组水平,鉴定党参Codonopsis pilosula WRKY转录因子家族成员,分析党参WRKY转录因子家族的特征,并探讨其在盐胁迫响应中的潜在作用,为研究党参WRKY转录因子功能奠定基础。方法 利用隐马尔可夫模型基于蛋白质保守结构域在全基因组范围内进行筛选潜在基因家族成员。利用MAFFT、IQ-TREE软件、MEME在线工具、Plant CARE和TBtools等完成蛋白序列比对、保守结构域、进化树分析、基因共线性情况和启动子区顺式作用元件分析。基于根、茎、叶和花不同组织的转录组数据分析WRKY基因的表达模式,并利用qRT-PCR进行WRKY基因相对表达量分析,另外结合党参在0、60、120 mmol/L NaCl处理的转录组数据分析WRKY基因在盐胁迫条件下的表达变化。结果 从党参中鉴定到50个WRKY转录因子成员,蛋白基序分析显示其均有典型的WRKY结构域WRKYGQK,与拟南芥和水稻的WRKY转录因子构建系统进化树,将党参50个WRKY转录因子分为3组,其中第2大组可分为5个亚群。党参WRKY成员编码的氨基酸长度在103~986氨基酸之间,等电点为4.87~9.99,相对分子质量为12 435.14~107 946.28。基因表达结果表明党参WRKY基因中CpWRKY26CpWRKY48CpWRKY2CpWRKY49在党参根、茎、叶和花中的表达水平具有显著差异性。盐胁迫处理结果表明,多数CpWRKY基因在不同浓度NaCl处理下呈现差异表达趋势,其中部分成员与已报道的抗盐WRKY基因在系统发育上聚类,提示其可能参与党参盐胁迫响应调控。结论 首次从全基因组水平对党参WRKY基因家族进行系统鉴定和生物信息学分析,并结合组织表达与盐胁迫响应分析揭示了党参WRKY基因可能参与党参生长发育、次生代谢物质生物合成及胁迫响应等生理过程,为深入研究党参WRKY基因的功能及其在药用成分调控中的作用机制奠定了理论基础,并为党参分子辅助育种提供了基因资源和科学依据。, authors=王春辉1,2, 宋敏1, 范潘慧2,3, 万会花2, 王飞飞4, 孙伟2, 曹雪2, 马静1, authorsList=王春辉, 宋敏, 范潘慧, 万会花, 王飞飞, 孙伟, 曹雪, 马静, authorCompany=1 青岛农业大学园艺学院 山东省园艺作物基因改良工程实验室, 山东 青岛 266109;
2 中国中医科学院中药研究所 道地药材品质保障与资源持续利用全国重点实验室, 北京 100700;
3 中国医学科学院 北京协和医学院药用植物研究所 国家中医药管理局中药资源保护重点研究室, 北京 100193;
4 云南特色植物提取实验室有限公司, 云南 昆明 650106, correspAuthors=曹雪, authorNote=王春辉: 王春辉,硕士研究生,研究方向为生物信息学。E-mail:20232107003@stu.qau.edu.cn, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=PfX9EIOM+TbNjTDpiM70BQ==, pdfFileSize=2230225, 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=国家重点研发计划项目 (2022YFC3501703); 云南特色植物提取实验室开放研究项目基金资助 (YKKF2024020))}, authors=null, keywords=[Keyword(id=1304401314092446215, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=CN, orderNo=1, keyword=党参), Keyword(id=1304401314201498120, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=CN, orderNo=2, keyword=WRKY转录因子), Keyword(id=1304401314331521545, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=CN, orderNo=3, keyword=全基因组鉴定), Keyword(id=1304401314457350666, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=CN, orderNo=4, keyword=盐胁迫), Keyword(id=1304401314578985483, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=CN, orderNo=5, keyword=功能分析), Keyword(id=1304401315006804492, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388085345705991, language=EN, orderNo=1, keyword=Codonopsis pilosula(Franch.) 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Luan F, Ji Y F, Peng L X, et al. Extraction, purification, structural characteristics and biological properties of the polysaccharides from Codonopsis pilosula: A review [J]. Carbohydr Polym, 2021, 261: 117863.
张向东, 高建平, 曹铃亚, 等. 中药党参资源及生产现状[J]. 中华中医药学刊, 2013, 31(3): 496-498.
王红燕, 陈垣, 郭凤霞, 等. 党参属种质资源多样性及可药用种质创新研究进展[J]. 中草药, 2024, 55(3): 978-988.
Eulgem T, Rushton P J, Robatzek S, et al. The WRKY superfamily of plant transcription factors [J]. Trends Plant Sci, 2000, 5(5): 199-206.
Ülker B, Somssich I E. WRKY transcription factors: From DNA binding towards biological function [J]. Curr Opin Plant Biol, 2004, 7(5): 491-498.
Bakshi M, Oelmüller R. WRKY transcription factors: Jack of many trades in plants [J]. Plant Signal Behav, 2014, 9(2): e27700.
Zhang Y J, Wang L J. The WRKY transcription factor superfamily: Its origin in eukaryotes and expansion in plants [J]. BMC Evol Biol, 2005, 5: 1.
Jiang J J, Ma S H, Ye N H, et al. WRKY transcription factors in plant responses to stresses [J]. J Integr Plant Biol, 2017, 59(2): 86-101.
Dong J X, Chen C H, Chen Z X. Expression profiles of the Arabidopsis WRKY gene superfamily during plant defense response [J]. Plant Mol Biol, 2003, 51(1): 21-37.
Wu K L, Guo Z J, Wang H H, et al. The WRKY family of transcription factors in rice and Arabidopsis and their origins [J]. DNA Res, 2005, 12(1): 9-26.
Zhao Z H, Wang R N, Su W H, et al. A comprehensive analysis of the WRKY family in soybean and functional analysis of GmWRKY164-GmGSL7c in resistance to soybean mosaic virus [J]. BMC Genom, 2024, 25(1): 620.
Huang S X, Gao Y F, Liu J K, et al. Genome-wide analysis of WRKY transcription factors in Solanum lycopersicum [J]. Mol Genet Genom, 2012, 287(6): 495-513.
Ciolkowski I, Wanke D, Birkenbihl R P, et al. Studies on DNA-binding selectivity of WRKY transcription factors lend structural clues into WRKY-domain function [J]. Plant Mol Biol, 2008, 68(1): 81-92.
Brand L H, Fischer N M, Harter K, et al. Elucidating the evolutionary conserved DNA-binding specificities of WRKY transcription factors by molecular dynamics and in vitro binding assays [J]. Nucleic Acids Res, 2013, 41(21): 9764-9778.
Chen T T, Li Y P, Xie L H, et al. AaWRKY17, a positive regulator of artemisinin biosynthesis, is involved in resistance to Pseudomonas syringae in Artemisia annua [J]. Hortic Res, 2021, 810.1038: s41438-21-00652-6.
van Verk M C, Bol J F, Linthorst H J. WRKY transcription factors involved in activation of SA biosynthesis genes [J]. BMC Plant Biol, 2011, 11(1): 89.
Sun Y D, Yu D Q. Activated expression of AtWRKY53 negatively regulates drought tolerance by mediating stomatal movement [J]. Plant Cell Rep, 2015, 34(8): 1295-1306.
Song Y S, Zheng H X, Sui Y, et al. SbWRKY55 regulates sorghum response to saline environment by its dual role in abscisic acid signaling [J]. Theor Appl Genet, 2022, 135(8): 2609-2625.
潘凌云, 马家冀, 李建民, 等. 植物盐胁迫应答转录因子的研究进展[J]. 生物工程学报, 2022, 38(1): 50-65.
Yang Y Q, Guo Y. Elucidating the molecular mechanisms mediating plant salt-stress responses [J]. New Phytol, 2018, 217(2): 523-539.
Munns R, Tester M. Mechanisms of salinity tolerance [J]. Annu Rev Plant Biol, 2008, 59: 651-681.
Ding Z J, Yan J Y, Li C X, et al. Transcription factor WRKY46 modulates the development of Arabidopsis lateral roots in osmotic/salt stress conditions via regulation of ABA signaling and auxin homeostasis [J]. Plant J, 2015, 84(1): 56-69.
Zhang Y Z, Li P, Niu Y Q, et al. Evolution of the WRKY66 gene family and its mutations generated by the CRISPR/Cas9 system increase the sensitivity to salt stress in Arabidopsis [J]. Int J Mol Sci, 2023, 24(4): 3071.
Tao Z, Kou Y J, Liu H B, et al. OsWRKY45 alleles play different roles in abscisic acid signalling and salt stress tolerance but similar roles in drought and cold tolerance in rice [J]. J Exp Bot, 2011, 62(14): 4863-4874.
Huang S Z, Hu L J, Zhang S H, et al. Rice OsWRKY50 mediates ABA-dependent seed germination and seedling growth, and ABA-independent salt stress tolerance [J]. Int J Mol Sci, 2021, 22(16): 8625.
Huang J J, Liu F H, Chao D, et al. The WRKY transcription factor OsWRKY54 is involved in salt tolerance in rice [J]. Int J Mol Sci, 2022, 23(19): 11999.
Yu J S, Cao X, Mi Y L, et al. Genome-wide analysis of WRKY gene family in high-CBD hemp (Cannabis sativa L.) and identification of the WRKY genes involved in abiotic stress responses and regulation cannabinoid accumulation [J]. Ind Crops Prod, 2024, 210: 118158.
Chen B Z, Yang Z J, Yang L, et al. Chromosome-scale genome assembly of Codonopsis pilosula and comparative genomic analyses shed light on its genome evolution [J]. Front Plant Sci, 2024, 15: 1469375.
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.
Xie J M, Chen Y R, Cai G J, et al. Tree Visualization By One Table (tvBOT): A web application for visualizing, modifying and annotating phylogenetic trees [J]. Nucleic Acids Res, 2023, 51(W1): W587-W592.
Gao S M, Liu J S, Wang M, et al. Traditional uses, phytochemistry, pharmacology and toxicology of Codonopsis: A review [J]. J Ethnopharmacol, 2018, 219: 50-70.
Rushton P J, Somssich I E, Ringler P, et al. WRKY transcription factors [J]. Trends Plant Sci, 2010, 15(5): 247-258.
Wani S H, Anand S, Singh B, et al. WRKY transcription factors and plant defense responses: Latest discoveries and future prospects [J]. Plant Cell Rep, 2021, 40(7): 1071-1085.
Baillo E H, Hanif M S, Guo Y H, et al. Genome-wide identification of WRKY transcription factor family members in sorghum (Sorghum bicolor (L.) moench) [J]. PLoS One, 2020, 15(8): e0236651.
Li C L, Li D Q, Shao F J, et al. Molecular cloning and expression analysis of WRKY transcription factor genes in Salvia miltiorrhiza [J]. BMC Genom, 2015, 16(1): 200.
Zhang G L, Sun Y E, Ullah N, et al. Changes in secondary metabolites contents and stress responses in Salvia miltiorrhiza via ScWRKY35 overexpression: Insights from a wild relative Salvia castanea [J]. Plant Physiol Biochem, 2024, 211: 108671.
Zheng L L, Qiu B L, Su L L, et al. Panax notoginseng WRKY transcription factor 9 is a positive regulator in responding to root rot pathogen Fusarium solani [J]. Front Plant Sci, 2022, 13: 930644.
Di P, Wang P, Yan M, et al. Genome-wide characterization and analysis of WRKY transcription factors in Panax ginseng [J]. BMC Genom, 2021, 22(1): 834.
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Guo D S, Zhang J Z, Wang X L, et al. The WRKY transcription factor WRKY71/EXB1 controls shoot branching by transcriptionally regulating RAX genes in Arabidopsis [J]. Plant Cell, 2015, 27(11): 3112-3127.
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党参中WRKY转录因子家族的鉴定及表达分析
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中草药 | 药材与资源 2026,57(10): 3940-3953
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中草药 |药材与资源 2026 , 57 (10) : 3940 -3953
党参中WRKY转录因子家族的鉴定及表达分析
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王春辉1,2, 宋敏1, 范潘慧2,3, 万会花2, 王飞飞4, 孙伟2, 曹雪2, 马静1
作者信息
    1 青岛农业大学园艺学院 山东省园艺作物基因改良工程实验室, 山东 青岛 266109;
    2 中国中医科学院中药研究所 道地药材品质保障与资源持续利用全国重点实验室, 北京 100700;
    3 中国医学科学院 北京协和医学院药用植物研究所 国家中医药管理局中药资源保护重点研究室, 北京 100193;
    4 云南特色植物提取实验室有限公司, 云南 昆明 650106
通讯作者:
曹雪
作者简介:
王春辉: 王春辉,硕士研究生,研究方向为生物信息学。E-mail:20232107003@stu.qau.edu.cn
Identification and expression analysis of WRKY transcription factor family in Codonopsis pilosula
  • WANG Chunhui, SONG Min, FAN Panhui, WAN Huihua, WANG Feifei, SUN Wei, CAO Xue, MA Jing
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.10.022
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    目的 在全基因组水平,鉴定党参Codonopsis pilosula WRKY转录因子家族成员,分析党参WRKY转录因子家族的特征,并探讨其在盐胁迫响应中的潜在作用,为研究党参WRKY转录因子功能奠定基础。方法 利用隐马尔可夫模型基于蛋白质保守结构域在全基因组范围内进行筛选潜在基因家族成员。利用MAFFT、IQ-TREE软件、MEME在线工具、Plant CARE和TBtools等完成蛋白序列比对、保守结构域、进化树分析、基因共线性情况和启动子区顺式作用元件分析。基于根、茎、叶和花不同组织的转录组数据分析WRKY基因的表达模式,并利用qRT-PCR进行WRKY基因相对表达量分析,另外结合党参在0、60、120 mmol/L NaCl处理的转录组数据分析WRKY基因在盐胁迫条件下的表达变化。结果 从党参中鉴定到50个WRKY转录因子成员,蛋白基序分析显示其均有典型的WRKY结构域WRKYGQK,与拟南芥和水稻的WRKY转录因子构建系统进化树,将党参50个WRKY转录因子分为3组,其中第2大组可分为5个亚群。党参WRKY成员编码的氨基酸长度在103~986氨基酸之间,等电点为4.87~9.99,相对分子质量为12 435.14~107 946.28。基因表达结果表明党参WRKY基因中CpWRKY26CpWRKY48CpWRKY2CpWRKY49在党参根、茎、叶和花中的表达水平具有显著差异性。盐胁迫处理结果表明,多数CpWRKY基因在不同浓度NaCl处理下呈现差异表达趋势,其中部分成员与已报道的抗盐WRKY基因在系统发育上聚类,提示其可能参与党参盐胁迫响应调控。结论 首次从全基因组水平对党参WRKY基因家族进行系统鉴定和生物信息学分析,并结合组织表达与盐胁迫响应分析揭示了党参WRKY基因可能参与党参生长发育、次生代谢物质生物合成及胁迫响应等生理过程,为深入研究党参WRKY基因的功能及其在药用成分调控中的作用机制奠定了理论基础,并为党参分子辅助育种提供了基因资源和科学依据。
    党参  /  WRKY转录因子  /  全基因组鉴定  /  盐胁迫  /  功能分析
    Objective To identify members of the WRKY transcription factor family in Codonopsis pilosula at the genome-wide level and analyze their characteristics, and explore their potential roles in response to salt stress, thereby laying a foundation for functional studies of C. pilosula WRKY transcription factors. Methods Potential gene family members were screened across the entire genome based on conserved protein domains using the Hidden Markov model (HMM). Protein sequence alignment, conserved domain analysis, phylogenetic tree construction, gene synteny analysis, and cis-acting element analysis in the promoter region were performed using software and online tools including MAFFT, IQ-TREE, MEME, Plant CARE and TBtools. Expression patterns of WRKY genes were analyzed based on transcriptome data from different tissues (roots, stems, leaves, and flowers) and qRT-PCR was used to determine their relative expression levels. In addition, the transcriptome data of C. pilosula treated with 0, 60, and 120 mmol/L NaCl were analyzed to examine the expression changes of WRKY genes under salt stress. Results A total of 50 WRKY transcription factor members were identified in C. pilosula. Motif analysis showed that all members contained the typical WRKY domain with the conserved sequence WRKYGQK. Phylogenetic analysis with WRKY transcription factors from Arabidopsis thaliana and Oryza sativa classified the 50 C. pilosula WRKY transcription factors into three groups, with group II further divided into five subgroups. The amino acid lengths of the identified WRKY proteins ranged from 103 to 986 residues, with isoelectric points (pI) of 4.87−9.99 and molecular weights (MW) of 12 435.14−107 946.28. Gene expression analysis revealed significant differences in the expression levels of CpWRKY26, CpWRKY48, CpWRKY2, and CpWRKY49 among roots, stems, leaves, and flowers of C. pilosula. The results of salt stress treatment indicated that most CpWRKY genes showed differential expression trends under different concentrations of NaCl, and some members cluster phylogenetically with previously reported salt-tolerant WRKY genes, suggesting that they may be involved in the regulation of C. pilosula salt stress responses. Conclusion This study represents the first systematic identification and bioinformatics analysis of the WRKY gene family in C. pilosula at the genome-wide level. By combining tissue expression and salt stress response analyses, the study reveales that the WRKY genes in C. pilosula may be involved in physiological processes such as growth and development, secondary metabolite biosynthesis, and stress responses. This lays a theoretical foundation for further research on the functions of WRKY genes and their roles in regulating medicinal components, and provides gene resources and scientific evidence for molecular-assisted breeding of C. pilosula.
    Codonopsis pilosula(Franch.) Nannf.  /  WRKY transcription factor  /  genome-wide identification  /  salt stress  /  functional analysis
    王春辉, 宋敏, 范潘慧, 万会花, 王飞飞, 孙伟, 曹雪, 马静. 党参中WRKY转录因子家族的鉴定及表达分析. 中草药, 2026 , 57 (10) : 3940 -3953 . DOI: 10.7501/j.issn.0253-2670.2026.10.022
    WANG Chunhui, SONG Min, FAN Panhui, WAN Huihua, WANG Feifei, SUN Wei, CAO Xue, MA Jing. Identification and expression analysis of WRKY transcription factor family in Codonopsis pilosula[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (10) : 3940 -3953 . DOI: 10.7501/j.issn.0253-2670.2026.10.022

      国家重点研发计划项目 (2022YFC3501703); 云南特色植物提取实验室开放研究项目基金资助 (YKKF2024020)

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    张欢, 李超, 汲晨锋. 药食同源党参化学成分、药理作用及应用研究进展[J]. 食品科学, 2024, 45(23): 338-348.
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    Wu K L, Guo Z J, Wang H H, et al. The WRKY family of transcription factors in rice and Arabidopsis and their origins [J]. DNA Res, 2005, 12(1): 9-26.
    Zhao Z H, Wang R N, Su W H, et al. A comprehensive analysis of the WRKY family in soybean and functional analysis of GmWRKY164-GmGSL7c in resistance to soybean mosaic virus [J]. BMC Genom, 2024, 25(1): 620.
    Huang S X, Gao Y F, Liu J K, et al. Genome-wide analysis of WRKY transcription factors in Solanum lycopersicum [J]. Mol Genet Genom, 2012, 287(6): 495-513.
    Ciolkowski I, Wanke D, Birkenbihl R P, et al. Studies on DNA-binding selectivity of WRKY transcription factors lend structural clues into WRKY-domain function [J]. Plant Mol Biol, 2008, 68(1): 81-92.
    Brand L H, Fischer N M, Harter K, et al. Elucidating the evolutionary conserved DNA-binding specificities of WRKY transcription factors by molecular dynamics and in vitro binding assays [J]. Nucleic Acids Res, 2013, 41(21): 9764-9778.
    Chen T T, Li Y P, Xie L H, et al. AaWRKY17, a positive regulator of artemisinin biosynthesis, is involved in resistance to Pseudomonas syringae in Artemisia annua [J]. Hortic Res, 2021, 810.1038: s41438-21-00652-6.
    van Verk M C, Bol J F, Linthorst H J. WRKY transcription factors involved in activation of SA biosynthesis genes [J]. BMC Plant Biol, 2011, 11(1): 89.
    Sun Y D, Yu D Q. Activated expression of AtWRKY53 negatively regulates drought tolerance by mediating stomatal movement [J]. Plant Cell Rep, 2015, 34(8): 1295-1306.
    Song Y S, Zheng H X, Sui Y, et al. SbWRKY55 regulates sorghum response to saline environment by its dual role in abscisic acid signaling [J]. Theor Appl Genet, 2022, 135(8): 2609-2625.
    潘凌云, 马家冀, 李建民, 等. 植物盐胁迫应答转录因子的研究进展[J]. 生物工程学报, 2022, 38(1): 50-65.
    Yang Y Q, Guo Y. Elucidating the molecular mechanisms mediating plant salt-stress responses [J]. New Phytol, 2018, 217(2): 523-539.
    Munns R, Tester M. Mechanisms of salinity tolerance [J]. Annu Rev Plant Biol, 2008, 59: 651-681.
    Ding Z J, Yan J Y, Li C X, et al. Transcription factor WRKY46 modulates the development of Arabidopsis lateral roots in osmotic/salt stress conditions via regulation of ABA signaling and auxin homeostasis [J]. Plant J, 2015, 84(1): 56-69.
    Zhang Y Z, Li P, Niu Y Q, et al. Evolution of the WRKY66 gene family and its mutations generated by the CRISPR/Cas9 system increase the sensitivity to salt stress in Arabidopsis [J]. Int J Mol Sci, 2023, 24(4): 3071.
    Tao Z, Kou Y J, Liu H B, et al. OsWRKY45 alleles play different roles in abscisic acid signalling and salt stress tolerance but similar roles in drought and cold tolerance in rice [J]. J Exp Bot, 2011, 62(14): 4863-4874.
    Huang S Z, Hu L J, Zhang S H, et al. Rice OsWRKY50 mediates ABA-dependent seed germination and seedling growth, and ABA-independent salt stress tolerance [J]. Int J Mol Sci, 2021, 22(16): 8625.
    Huang J J, Liu F H, Chao D, et al. The WRKY transcription factor OsWRKY54 is involved in salt tolerance in rice [J]. Int J Mol Sci, 2022, 23(19): 11999.
    Yu J S, Cao X, Mi Y L, et al. Genome-wide analysis of WRKY gene family in high-CBD hemp (Cannabis sativa L.) and identification of the WRKY genes involved in abiotic stress responses and regulation cannabinoid accumulation [J]. Ind Crops Prod, 2024, 210: 118158.
    Chen B Z, Yang Z J, Yang L, et al. Chromosome-scale genome assembly of Codonopsis pilosula and comparative genomic analyses shed light on its genome evolution [J]. Front Plant Sci, 2024, 15: 1469375.
    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.
    Xie J M, Chen Y R, Cai G J, et al. Tree Visualization By One Table (tvBOT): A web application for visualizing, modifying and annotating phylogenetic trees [J]. Nucleic Acids Res, 2023, 51(W1): W587-W592.
    Gao S M, Liu J S, Wang M, et al. Traditional uses, phytochemistry, pharmacology and toxicology of Codonopsis: A review [J]. J Ethnopharmacol, 2018, 219: 50-70.
    Rushton P J, Somssich I E, Ringler P, et al. WRKY transcription factors [J]. Trends Plant Sci, 2010, 15(5): 247-258.
    Wani S H, Anand S, Singh B, et al. WRKY transcription factors and plant defense responses: Latest discoveries and future prospects [J]. Plant Cell Rep, 2021, 40(7): 1071-1085.
    Baillo E H, Hanif M S, Guo Y H, et al. Genome-wide identification of WRKY transcription factor family members in sorghum (Sorghum bicolor (L.) moench) [J]. PLoS One, 2020, 15(8): e0236651.
    Li C L, Li D Q, Shao F J, et al. Molecular cloning and expression analysis of WRKY transcription factor genes in Salvia miltiorrhiza [J]. BMC Genom, 2015, 16(1): 200.
    Zhang G L, Sun Y E, Ullah N, et al. Changes in secondary metabolites contents and stress responses in Salvia miltiorrhiza via ScWRKY35 overexpression: Insights from a wild relative Salvia castanea [J]. Plant Physiol Biochem, 2024, 211: 108671.
    Zheng L L, Qiu B L, Su L L, et al. Panax notoginseng WRKY transcription factor 9 is a positive regulator in responding to root rot pathogen Fusarium solani [J]. Front Plant Sci, 2022, 13: 930644.
    Di P, Wang P, Yan M, et al. Genome-wide characterization and analysis of WRKY transcription factors in Panax ginseng [J]. BMC Genom, 2021, 22(1): 834.
    Song A P, Li P L, Jiang J F, et al. Phylogenetic and transcription analysis of Chrysanthemum WRKY transcription factors [J]. Int J Mol Sci, 2014, 15(8): 14442-14455.
    Guo D S, Zhang J Z, Wang X L, et al. The WRKY transcription factor WRKY71/EXB1 controls shoot branching by transcriptionally regulating RAX genes in Arabidopsis [J]. Plant Cell, 2015, 27(11): 3112-3127.
    Cai Y H, Chen X J, Xie K, et al. Dlf1, a WRKY transcription factor, is involved in the control of flowering time and plant height in rice [J]. PLoS One, 2014, 9(7): e102529.
    Zhao S S, Zhang Q K, Liu M Y, et al. Regulation of plant responses to salt stress [J]. Int J Mol Sci, 2021, 22(9): 4609.
    Zhou H P, Shi H F, Yang Y Q, et al. Insights into plant salt stress signaling and tolerance [J]. J Genet Genom, 2024, 51(1): 16-34.
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    2026年第57卷第10期
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    doi: 10.7501/j.issn.0253-2670.2026.10.022
    • 接收时间:2026-01-03
    • 首发时间:2026-09-09
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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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