Article(id=1304406875978617675, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.02.022, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1759334400000, receivedDateStr=2025-10-02, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924433941, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924433941, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924433941, creator=13701087609, updateTime=1788924433941, updator=13701087609, issue=Issue{id=1304406828071281069, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='2', pageStart='393', pageEnd='788', issueExtLink='null', onlineDate='null', pubDate='1769529600000', pubDateStr='2026-01-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924422518, creator='13701087609', updateTime=1788924652596, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407793138688830, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407793138688831, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=627, endPage=639, ext={EN=ArticleExt(id=1304406877769585486, articleId=1304406875978617675, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Identification and functional study of ERF gene family in Trichosanthes kirilowii based on transcriptome and sRNA sequencing, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=ObjectiveTo identify the members of the ERF gene family (TkERFs) of Trichosanthes kirilowii based on transcriptome sequencing data, and to analyze their biological functions in the growth and development of T. kirilowii, so as to provide a theoretical basis for further studying the mechanism of sex differentiation in T. kirilowii. Methods Bioinformatics methods were used to systematically identify the ERF gene family members of T. kirilowii, and the key candidate gene for sex differentiation, TkERF2, was screened for functional elucidation. The tissue expression patterns of the tissues were analyzed by real-time fluorescence quantitative PCR (qRT-PCR). The TkERF2 overexpression vector was constructed and its biological function was explored through subcellular localization and genetic transformation experiments of Arabidopsis thaliana, combined with phenotypic observation, related gene expression detection and ethylene content determination. Transcriptome and small RNA omics data were integrated to screen miRNAs that target the regulation of TkERFs and improve their regulatory networks. Results Based on transcriptome data, a total of 54 TkERF genes (TkERF1TkERF54) were identified by open reading frame (ORF) and conserved domain analysis. It encodes a protein sequence length of 101—389 amino acids, a molecular weight of 11 580—43 310, and a theoretical isoelectric point (pI) of 4.66—10.60. Subcellular localization prediction showed that 74% of TkERFs were localized in the nucleus and 26% were distributed in chloroplasts and cytoplasm. Protein conservation motif analysis identified 10 motifs. The phylogenetic tree divides the family into eight subfamilies. TkERF2, TkERF20 and TkERF45 were identified by specific miRNA targeting. Transgenic A. thaliana experiments showed that TkERF2 significantly regulated ethylene synthesis pathway, and the expressions of auxin synthesis genes (AtYUC2, AtYUC6), auxin response factor (AtARF8) and auxin transport gene (AtPIN2) were significantly higher than those of wild type (P < 0.05), confirming that TkERF2 was involved in developmental process by positively regulating auxin synthesis and transport. Conclusion This study has completed the systematic identification and preliminary exploration of the ERF gene family, which provides a theoretical basis for analyzing the mechanism of sex determination and genetic improvement of T. kirilowii., authors=ONG Jiahui, ZHANG Wenyu, HU Xiuqin, YU Xiuyue, ZHANG Xiaozhen, XIN Jie, authorsList=ONG Jiahui, ZHANG Wenyu, HU Xiuqin, YU Xiuyue, ZHANG Xiaozhen, XIN Jie, 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=1304406877647950669, articleId=1304406875978617675, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=基于转录组与sRNA测序的栝楼ERF基因家族鉴定及功能研究, columnId=1304140203967410414, journalTitle=中草药, columnName=药材与资源, runingTitle=null, highlight=null, articleAbstract=目的 基于转录组测序数据鉴定栝楼Trichosanthes kirilowii ERF基因家族(TkERFs)成员,解析其在栝楼生长发育中的生物学功能,为深入研究栝楼性别分化机制提供理论依据。方法 采用生物信息学方法系统鉴定栝楼ERF基因家族成员,并筛选性别分化关键候选基因TkERF2进行功能解析。利用实时荧光定量PCR(qRT-PCR)技术分析其组织表达模式;构建TkERF2过表达载体,通过亚细胞定位及拟南芥遗传转化实验,结合表型观察、相关基因表达量检测及乙烯含量测定,探究其生物学功能;整合转录组与small RNA组学数据,筛选靶向调控TkERFs的miRNAs,完善其调控网络。结果 基于转录组数据,经开放阅读框(open reading frame,ORF)及保守结构域分析,共鉴定出54个TkERF基因(TkERF1TkERF54)。其编码蛋白序列长度为101~389个氨基酸,相对分子质量为11 580~43 310,理论等电点(pI)为4.66~10.60。亚细胞定位预测显示74%的TkERFs定位于细胞核,26%分布于叶绿体及细胞质。蛋白质保守基序分析鉴定出10种motif。系统发育树将该家族划分为8个亚族。筛选鉴定出TkERF2TkERF20TkERF45受特异性miRNA靶向调控。转基因拟南芥实验表明,TkERF2显著调控乙烯合成途径,且生长素合成基因(AtYUC2AtYUC6)、生长素响应因子(AtARF8)及生长素转运基因(AtPIN2)的表达量均显著高于野生型(P<0.05),证实TkERF2通过正向调控生长素合成与转运参与发育进程。结论 完成栝楼ERF基因家族的系统鉴定与功能初探,为解析栝楼性别决定机制及遗传改良提供了理论基础。, authors=宋佳辉1, 张文玉1, 胡秀芹1, 于秀月1, 张效振1, 辛杰1, authorsList=宋佳辉, 张文玉, 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张琪, 彭向前. 栝楼的活性成分及其药理作用的研究进展[J]. 山东化工, 2021(14):98-100.
彭星星, 李卫文, 董玲, 等. 栝楼食用历史沿革与变迁[J]. 皖西学院学报, 2023, 39(2):79-83.
周涛, 黄璐琦, 江维克. 栝楼属(葫芦科)植物的系统演化与地理分布[J]. 植物科学学报, 2015, 33(3):414-423.
辛杰, 王振, 张波, 等. 栝楼不同性别花芽分化形态解剖特征观察[J]. 植物科学学报, 2018, 36(5):648-657.
方圆, 朱衎, 吴慧平, 等. 安徽省首次发现肾形肾状线虫危害瓜蒌[J]. 植物保护, 2023, 49(6):87-94.
汪霞, 林一帆, 张立新. 栝楼主要病害及综合防治技术[J]. 特种经济动植物, 2021, 24(8):40-41.
Rao Y R, Ansari M W, Sahoo R K, et al. Salicylic acid modulates ACS, NHX1, sos1 and HKT12 expression to regulate ethylene overproduction and Na+ ions toxicity that leads to improved physiological status and enhanced salinity stress tolerance in tomato plants cv. Pusa Ruby[J]. Plant Signal Behav, 2021, 16(11):1950888.
Wang Z Y, Yadav V, Yan X, et al. Systematic genome-wide analysis of the ethylene-responsive ACS gene family:Contributions to sex form differentiation and development in melon and watermelon[J]. Gene, 2021, 805:145910.
Cebrián G, Iglesias-Moya J, Romero J, et al. The ethylene biosynthesis gene CpACO1A:A new player in the regulation of sex determination and female flower development in Cucurbita pepo[J]. Front Plant Sci, 2022, 12:817922.
Boualem A, Fergany M, Fernandez R, et al. A conserved mutation in an ethylene biosynthesis enzyme leads to andromonoecy in melons[J]. Science, 2008, 321(5890):836-838.
Boualem A, Troadec C, Camps C, et al. A cucurbit androecy gene reveals how unisexual flowers develop and dioecy emerges[J]. Science, 2015, 350(6261):688-691.
Kamachi S, Sekimoto H, Kondo N, et al. Cloning of a cDNA for a 1-aminocyclopropane-1-carboxylate synthase that is expressed during development of female flowers at the apices of Cucumis sativus L[J]. Plant Cell Physiol, 1997, 38(11):1197-1206.
Saito S, Fujii N, Miyazawa Y, et al. Correlation between development of female flower buds and expression of the CS-ACS2 gene in cucumber plants[J]. J Exp Bot, 2007, 58(11):2897-2907.
Martínez C, Jamilena M. To be a male or a female flower, a question of ethylene in cucurbits[J]. Curr Opin Plant Biol, 2021, 59:101981.
Wu Y, Li X, Zhang J N, et al. ERF subfamily transcription factors and their function in plant responses to abiotic stresses[J]. Front Plant Sci, 2022, 13:1042084.
牛欢欢. 黄瓜乙烯响应因子ERFs参与性别决定过程的调控研究[D]. 杨凌:西北农林科技大学, 2021.
Pan J, Wen H F, Chen G Q, et al. A positive feedback loop mediated by CsERF31 initiates female cucumber flower development:Ethylene Response Factor31 mediates a positive feedback loop that initiates female cucumber flower development[J]. Plant Physiol, 2021, 186(2):1088-1100.
Tao Q Y, Niu H H, Wang Z Y, et al. Ethylene responsive factor ERF110 mediates ethylene-regulated transcription of a sex determination-related orthologous gene in two Cucumis species[J]. J Exp Bot, 2018, 69(12):2953-2965.
Hu X Q, Liao Z Y, Zhang B, et al. Transcriptome sequencing and screening of genes related to sex determination of Trichosanthes kirilowii Maxim[J]. PLoS One, 2020, 15(10):e0239230.
Hu X Q, Song H, Li N, et al. Identification and analysis of miRNAs differentially expressed in male and female Trichosanthes kirilowii Maxim[J]. BMC Genomics, 2023, 24(1):81.
Wang K, Zhai M J, Cui D Z, et al. Genome-wide analysis of the amino acid permeases gene family in wheat and TaAAP1 enhanced salt tolerance by accumulating ethylene[J]. Int J Mol Sci, 2023, 24(18):13800.
Tran D, Dauphin A, Meimoun P, et al. Methanol induces cytosolic calcium variations, membrane depolarization and ethylene production in Arabidopsis and tobacco[J]. Ann Bot, 2018, 122(5):849-860.
Qiao H, Shen Z X, Huang S C, et al. Processing and subcellular trafficking of ER-tethered EIN2 control response to ethylene gas[J]. Science, 2012, 338(6105):390-393.
Nakano T, Suzuki K, Fujimura T, et al. Genome-wide analysis of the ERF gene family in Arabidopsis and rice[J]. Plant Physiol, 2006, 140(2):411-432.
Hu L F, Liu S Q. Genome-wide identification and phylogenetic analysis of the ERF gene family in cucumbers[J]. Genet Mol Biol, 2011, 34(4):624-633.
Li Q F, Zhang L, Chen P W, et al. Genome-wide identification of APETALA2/ETHYLENE RESPONSIVE FACTOR transcription factors in Cucurbita moschata and their involvement in ethylene response[J]. Front Plant Sci, 2022, 13:847754.
吴婧, 范菠菠, 张学峰, 等. 蒙古冰草ERF转录因子生物信息学及其表达分析[J]. 草地学报, 2022, 30(11):2910-2921.
杨金荣, 崔婉宁, 张瑜, 等. 基于转录组数据的半夏AP2/ERF基因家族鉴定及逆境响应分析[J]. 中国实验方剂学杂志, 2023, 29(5):176-184.
Holland P W H, Marlétaz F, Maeso I, et al. New genes from old:Asymmetric divergence of gene duplicates and the evolution of development[J]. Philos Trans R Soc Lond B Biol Sci, 2017, 372(1713):20150480.
Zafar M M, Rehman A, Razzaq A, et al. Genome-wide characterization and expression analysis of Erf gene family in cotton[J]. BMC Plant Biol, 2022, 22(1):134.
Li Z, Zhang Y, Ren J, et al. Ethylene-responsive factor ERF114 mediates fungal pathogen effector PevD1-induced disease resistance in Arabidopsis thaliana[J]. Mol Plant Pathol, 2022, 23(6):819-831.
Zheng L J, Nagpal P, Villarino G, et al. miR167 limits anther growth to potentiate anther dehiscence[J]. Development, 2019, 146(14):dev174375.
Wu M F, Tian Q, Reed J W. Arabidopsis microRNA167 controls patterns of ARF6 and ARF8 expression, and regulates both female and male reproduction[J]. Development, 2006, 133(21):4211-4218.
Shikata M, Yamaguchi H, Sasaki K, et al. Overexpression of Arabidopsis miR157b induces bushy architecture and delayed phase transition in Torenia fournieri[J]. Planta, 2012, 236(4):1027-1035.
Wu G, Park M Y, Conway S R, et al. The sequential action of miR156 and miR172 regulates developmental timing in Arabidopsis[J]. Cell, 2009, 138(4):750-759.
Wang J W, Czech B, Weigel D. miR156-regulated SPL transcription factors define an endogenous flowering pathway in Arabidopsis thaliana[J]. Cell, 2009, 138(4):738-749.
Hajieghrari B, Farrokhi N, Goliaei B, et al. Computational identification of microRNAs and their transcript target(s) in field mustard (Brassica rapa L.)[J]. Iran J Biotechnol, 2017, 15(1):22-32.
Kapadia C, Datta R, Mahammad S M, et al. Genome-wide identification, quantification, and validation of differentially expressed miRNAs in eggplant (Solanum melongena L.) based on their response to Ralstonia solanacearum infection[J]. ACS Omega, 2023, 8(2):2648-2657.
Tominaga-Wada R, Nukumizu Y, Wada T. Flowering is delayed by mutations in homologous genes CAPRICE and TRYPTICHON in the early flowering Arabidopsis cpl3 mutant[J]. J Plant Physiol, 2013, 170(16):1466-1468.
Cho L H, Yoon J, An G. The control of flowering time by environmental factors[J]. Plant J, 2017, 90(4):708-719.
Luccioni L, Krzymuski M, Sánchez-Lamas M, et al. Constans delays Arabidopsis flowering under short days[J]. Plant J, 2019, 97(5):923-932.
Xie Y R, Zhou Q, Zhao Y P, et al. FHY3 and FAR1 integrate light signals with the miR156-SPL module-mediated aging pathway to regulate Arabidopsis flowering[J]. Mol Plant, 2020, 13(3):483-498.)
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基于转录组与sRNA测序的栝楼ERF基因家族鉴定及功能研究
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宋佳辉, 张文玉, 胡秀芹, 于秀月, 张效振, 辛杰
中草药 | 药材与资源 2026,57(2): 627-639
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中草药 |药材与资源 2026 , 57 (2) : 627 -639
基于转录组与sRNA测序的栝楼ERF基因家族鉴定及功能研究
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宋佳辉, 张文玉, 胡秀芹, 于秀月, 张效振, 辛杰
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通讯作者:
辛杰
作者简介:
宋佳辉: 宋佳辉(2004—),女,中药学专业。E-mail: 2776612418@qq.com
Identification and functional study of ERF gene family in Trichosanthes kirilowii based on transcriptome and sRNA sequencing
ONG Jiahui, ZHANG Wenyu, HU Xiuqin, YU Xiuyue, ZHANG Xiaozhen, XIN Jie
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doi: 10.7501/j.issn.0253-2670.2026.02.022
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目的 基于转录组测序数据鉴定栝楼Trichosanthes kirilowii ERF基因家族(TkERFs)成员,解析其在栝楼生长发育中的生物学功能,为深入研究栝楼性别分化机制提供理论依据。方法 采用生物信息学方法系统鉴定栝楼ERF基因家族成员,并筛选性别分化关键候选基因TkERF2进行功能解析。利用实时荧光定量PCR(qRT-PCR)技术分析其组织表达模式;构建TkERF2过表达载体,通过亚细胞定位及拟南芥遗传转化实验,结合表型观察、相关基因表达量检测及乙烯含量测定,探究其生物学功能;整合转录组与small RNA组学数据,筛选靶向调控TkERFs的miRNAs,完善其调控网络。结果 基于转录组数据,经开放阅读框(open reading frame,ORF)及保守结构域分析,共鉴定出54个TkERF基因(TkERF1TkERF54)。其编码蛋白序列长度为101~389个氨基酸,相对分子质量为11 580~43 310,理论等电点(pI)为4.66~10.60。亚细胞定位预测显示74%的TkERFs定位于细胞核,26%分布于叶绿体及细胞质。蛋白质保守基序分析鉴定出10种motif。系统发育树将该家族划分为8个亚族。筛选鉴定出TkERF2TkERF20TkERF45受特异性miRNA靶向调控。转基因拟南芥实验表明,TkERF2显著调控乙烯合成途径,且生长素合成基因(AtYUC2AtYUC6)、生长素响应因子(AtARF8)及生长素转运基因(AtPIN2)的表达量均显著高于野生型(P<0.05),证实TkERF2通过正向调控生长素合成与转运参与发育进程。结论 完成栝楼ERF基因家族的系统鉴定与功能初探,为解析栝楼性别决定机制及遗传改良提供了理论基础。
栝楼  /  ERF基因  /  性别分化  /  乙烯  /  生长素
ObjectiveTo identify the members of the ERF gene family (TkERFs) of Trichosanthes kirilowii based on transcriptome sequencing data, and to analyze their biological functions in the growth and development of T. kirilowii, so as to provide a theoretical basis for further studying the mechanism of sex differentiation in T. kirilowii. Methods Bioinformatics methods were used to systematically identify the ERF gene family members of T. kirilowii, and the key candidate gene for sex differentiation, TkERF2, was screened for functional elucidation. The tissue expression patterns of the tissues were analyzed by real-time fluorescence quantitative PCR (qRT-PCR). The TkERF2 overexpression vector was constructed and its biological function was explored through subcellular localization and genetic transformation experiments of Arabidopsis thaliana, combined with phenotypic observation, related gene expression detection and ethylene content determination. Transcriptome and small RNA omics data were integrated to screen miRNAs that target the regulation of TkERFs and improve their regulatory networks. Results Based on transcriptome data, a total of 54 TkERF genes (TkERF1TkERF54) were identified by open reading frame (ORF) and conserved domain analysis. It encodes a protein sequence length of 101—389 amino acids, a molecular weight of 11 580—43 310, and a theoretical isoelectric point (pI) of 4.66—10.60. Subcellular localization prediction showed that 74% of TkERFs were localized in the nucleus and 26% were distributed in chloroplasts and cytoplasm. Protein conservation motif analysis identified 10 motifs. The phylogenetic tree divides the family into eight subfamilies. TkERF2, TkERF20 and TkERF45 were identified by specific miRNA targeting. Transgenic A. thaliana experiments showed that TkERF2 significantly regulated ethylene synthesis pathway, and the expressions of auxin synthesis genes (AtYUC2, AtYUC6), auxin response factor (AtARF8) and auxin transport gene (AtPIN2) were significantly higher than those of wild type (P < 0.05), confirming that TkERF2 was involved in developmental process by positively regulating auxin synthesis and transport. Conclusion This study has completed the systematic identification and preliminary exploration of the ERF gene family, which provides a theoretical basis for analyzing the mechanism of sex determination and genetic improvement of T. kirilowii.
Trichosanthes kirilowii Maxim.  /  ERF gene  /  gender differentiation  /  ethylene  /  auxin
宋佳辉, 张文玉, 胡秀芹, 于秀月, 张效振, 辛杰. 基于转录组与sRNA测序的栝楼ERF基因家族鉴定及功能研究. 中草药, 2026 , 57 (2) : 627 -639 . DOI: 10.7501/j.issn.0253-2670.2026.02.022
ONG Jiahui, ZHANG Wenyu, HU Xiuqin, YU Xiuyue, ZHANG Xiaozhen, XIN Jie. Identification and functional study of ERF gene family in Trichosanthes kirilowii based on transcriptome and sRNA sequencing[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (2) : 627 -639 . DOI: 10.7501/j.issn.0253-2670.2026.02.022

    山东省自然基金面上项目 (ZR2024MH046); 山东省大学生创新创业项目 (202510452030)

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张琪, 彭向前. 栝楼的活性成分及其药理作用的研究进展[J]. 山东化工, 2021(14):98-100.
彭星星, 李卫文, 董玲, 等. 栝楼食用历史沿革与变迁[J]. 皖西学院学报, 2023, 39(2):79-83.
周涛, 黄璐琦, 江维克. 栝楼属(葫芦科)植物的系统演化与地理分布[J]. 植物科学学报, 2015, 33(3):414-423.
辛杰, 王振, 张波, 等. 栝楼不同性别花芽分化形态解剖特征观察[J]. 植物科学学报, 2018, 36(5):648-657.
方圆, 朱衎, 吴慧平, 等. 安徽省首次发现肾形肾状线虫危害瓜蒌[J]. 植物保护, 2023, 49(6):87-94.
汪霞, 林一帆, 张立新. 栝楼主要病害及综合防治技术[J]. 特种经济动植物, 2021, 24(8):40-41.
Rao Y R, Ansari M W, Sahoo R K, et al. Salicylic acid modulates ACS, NHX1, sos1 and HKT12 expression to regulate ethylene overproduction and Na+ ions toxicity that leads to improved physiological status and enhanced salinity stress tolerance in tomato plants cv. Pusa Ruby[J]. Plant Signal Behav, 2021, 16(11):1950888.
Wang Z Y, Yadav V, Yan X, et al. Systematic genome-wide analysis of the ethylene-responsive ACS gene family:Contributions to sex form differentiation and development in melon and watermelon[J]. Gene, 2021, 805:145910.
Cebrián G, Iglesias-Moya J, Romero J, et al. The ethylene biosynthesis gene CpACO1A:A new player in the regulation of sex determination and female flower development in Cucurbita pepo[J]. Front Plant Sci, 2022, 12:817922.
Boualem A, Fergany M, Fernandez R, et al. A conserved mutation in an ethylene biosynthesis enzyme leads to andromonoecy in melons[J]. Science, 2008, 321(5890):836-838.
Boualem A, Troadec C, Camps C, et al. A cucurbit androecy gene reveals how unisexual flowers develop and dioecy emerges[J]. Science, 2015, 350(6261):688-691.
Kamachi S, Sekimoto H, Kondo N, et al. Cloning of a cDNA for a 1-aminocyclopropane-1-carboxylate synthase that is expressed during development of female flowers at the apices of Cucumis sativus L[J]. Plant Cell Physiol, 1997, 38(11):1197-1206.
Saito S, Fujii N, Miyazawa Y, et al. Correlation between development of female flower buds and expression of the CS-ACS2 gene in cucumber plants[J]. J Exp Bot, 2007, 58(11):2897-2907.
Martínez C, Jamilena M. To be a male or a female flower, a question of ethylene in cucurbits[J]. Curr Opin Plant Biol, 2021, 59:101981.
Wu Y, Li X, Zhang J N, et al. ERF subfamily transcription factors and their function in plant responses to abiotic stresses[J]. Front Plant Sci, 2022, 13:1042084.
牛欢欢. 黄瓜乙烯响应因子ERFs参与性别决定过程的调控研究[D]. 杨凌:西北农林科技大学, 2021.
Pan J, Wen H F, Chen G Q, et al. A positive feedback loop mediated by CsERF31 initiates female cucumber flower development:Ethylene Response Factor31 mediates a positive feedback loop that initiates female cucumber flower development[J]. Plant Physiol, 2021, 186(2):1088-1100.
Tao Q Y, Niu H H, Wang Z Y, et al. Ethylene responsive factor ERF110 mediates ethylene-regulated transcription of a sex determination-related orthologous gene in two Cucumis species[J]. J Exp Bot, 2018, 69(12):2953-2965.
Hu X Q, Liao Z Y, Zhang B, et al. Transcriptome sequencing and screening of genes related to sex determination of Trichosanthes kirilowii Maxim[J]. PLoS One, 2020, 15(10):e0239230.
Hu X Q, Song H, Li N, et al. Identification and analysis of miRNAs differentially expressed in male and female Trichosanthes kirilowii Maxim[J]. BMC Genomics, 2023, 24(1):81.
Wang K, Zhai M J, Cui D Z, et al. Genome-wide analysis of the amino acid permeases gene family in wheat and TaAAP1 enhanced salt tolerance by accumulating ethylene[J]. Int J Mol Sci, 2023, 24(18):13800.
Tran D, Dauphin A, Meimoun P, et al. Methanol induces cytosolic calcium variations, membrane depolarization and ethylene production in Arabidopsis and tobacco[J]. Ann Bot, 2018, 122(5):849-860.
Qiao H, Shen Z X, Huang S C, et al. Processing and subcellular trafficking of ER-tethered EIN2 control response to ethylene gas[J]. Science, 2012, 338(6105):390-393.
Nakano T, Suzuki K, Fujimura T, et al. Genome-wide analysis of the ERF gene family in Arabidopsis and rice[J]. Plant Physiol, 2006, 140(2):411-432.
Hu L F, Liu S Q. Genome-wide identification and phylogenetic analysis of the ERF gene family in cucumbers[J]. Genet Mol Biol, 2011, 34(4):624-633.
Li Q F, Zhang L, Chen P W, et al. Genome-wide identification of APETALA2/ETHYLENE RESPONSIVE FACTOR transcription factors in Cucurbita moschata and their involvement in ethylene response[J]. Front Plant Sci, 2022, 13:847754.
吴婧, 范菠菠, 张学峰, 等. 蒙古冰草ERF转录因子生物信息学及其表达分析[J]. 草地学报, 2022, 30(11):2910-2921.
杨金荣, 崔婉宁, 张瑜, 等. 基于转录组数据的半夏AP2/ERF基因家族鉴定及逆境响应分析[J]. 中国实验方剂学杂志, 2023, 29(5):176-184.
Holland P W H, Marlétaz F, Maeso I, et al. New genes from old:Asymmetric divergence of gene duplicates and the evolution of development[J]. Philos Trans R Soc Lond B Biol Sci, 2017, 372(1713):20150480.
Zafar M M, Rehman A, Razzaq A, et al. Genome-wide characterization and expression analysis of Erf gene family in cotton[J]. BMC Plant Biol, 2022, 22(1):134.
Li Z, Zhang Y, Ren J, et al. Ethylene-responsive factor ERF114 mediates fungal pathogen effector PevD1-induced disease resistance in Arabidopsis thaliana[J]. Mol Plant Pathol, 2022, 23(6):819-831.
Zheng L J, Nagpal P, Villarino G, et al. miR167 limits anther growth to potentiate anther dehiscence[J]. Development, 2019, 146(14):dev174375.
Wu M F, Tian Q, Reed J W. Arabidopsis microRNA167 controls patterns of ARF6 and ARF8 expression, and regulates both female and male reproduction[J]. Development, 2006, 133(21):4211-4218.
Shikata M, Yamaguchi H, Sasaki K, et al. Overexpression of Arabidopsis miR157b induces bushy architecture and delayed phase transition in Torenia fournieri[J]. Planta, 2012, 236(4):1027-1035.
Wu G, Park M Y, Conway S R, et al. The sequential action of miR156 and miR172 regulates developmental timing in Arabidopsis[J]. Cell, 2009, 138(4):750-759.
Wang J W, Czech B, Weigel D. miR156-regulated SPL transcription factors define an endogenous flowering pathway in Arabidopsis thaliana[J]. Cell, 2009, 138(4):738-749.
Hajieghrari B, Farrokhi N, Goliaei B, et al. Computational identification of microRNAs and their transcript target(s) in field mustard (Brassica rapa L.)[J]. Iran J Biotechnol, 2017, 15(1):22-32.
Kapadia C, Datta R, Mahammad S M, et al. Genome-wide identification, quantification, and validation of differentially expressed miRNAs in eggplant (Solanum melongena L.) based on their response to Ralstonia solanacearum infection[J]. ACS Omega, 2023, 8(2):2648-2657.
Tominaga-Wada R, Nukumizu Y, Wada T. Flowering is delayed by mutations in homologous genes CAPRICE and TRYPTICHON in the early flowering Arabidopsis cpl3 mutant[J]. J Plant Physiol, 2013, 170(16):1466-1468.
Cho L H, Yoon J, An G. The control of flowering time by environmental factors[J]. Plant J, 2017, 90(4):708-719.
Luccioni L, Krzymuski M, Sánchez-Lamas M, et al. Constans delays Arabidopsis flowering under short days[J]. Plant J, 2019, 97(5):923-932.
Xie Y R, Zhou Q, Zhao Y P, et al. FHY3 and FAR1 integrate light signals with the miR156-SPL module-mediated aging pathway to regulate Arabidopsis flowering[J]. Mol Plant, 2020, 13(3):483-498.
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doi: 10.7501/j.issn.0253-2670.2026.02.022
  • 接收时间:2025-10-02
  • 首发时间:2026-09-09
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  • 收稿日期:2025-10-02
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https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.02.022
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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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