防风AP2/ERF转录因子家族鉴定与表达分析OA
Identification and Expression Analysis of the AP2/ERF Transcription Factor Family in Saposhnikovia divaricata
为研究2种种源防风的SdAP2/ERF表达模式,筛选影响不同种源防风生长特性差异的AP2/ERF转录因子,利用生物信息学方法对防风AP2/ERF基因家族进行鉴定和功能分析,并通过qRT-PCR验证基因在不同种源防风中的表达模式,研究其在防风生长发育中的作用,确定关键调控基因.结果表明,从防风基因组中鉴定出208个AP2/ERF基因,并将其分为5个亚家族(AP2、ERF、DREB、RAV和Soloist),它们的蛋白质结构具有1个或多个保守的AP2结构域,通常不稳定且亲水.基序分析显示,除了 AP2/ERF结构域外,其他保守区域在系统发育树的不同分支中选择性分布.顺式作用元件分析显示,AP2/ERF家族基因的启动子区域显著富集与光响应、植物激素信号转导及非生物胁迫应答相关的调控元件.染色体定位结果显示,AP2/ERF基因在8条染色体上分布不均.种内共线性分析表明,AP2/ERF基因中有71对共线基因;种间共线性分析显示,SdAP2/ERF基因与胡萝卜同源基因进化关系更为相近.转录组分析表明,相较于BC防风,CC防风出现显著性差异表达基因,SdERF08、SdERF07、SdERF09、SdERF28显著性高表达,可能与其生长特征密切相关.
To investigate the expression patterns of SdAP2/ERF in 2 provenances of Saposhnikovia di-varicata and to screen AP2/ERF transcription factors influencing the differences in growth character-istics between the different provenances,bioinformatics methods were employed to identify and func-tionally analyze the AP2/ERF gene family in Saposhnikovia divaricata.The expression patterns of these genes in different provenances of Saposhnikovia divaricata were validated by qRT-PCR to study their roles in the growth and development of Saposhnikovia divaricata and to identify key regulatory genes.The results showed that 208 AP2/ERF genes were identified from the Saposhnikovia divarica-ta genome and classified into five subfamilies(AP2,ERF,DREB,RAV,and Soloist).Their encoded proteins contained one or more conserved AP2 domains and were generally unstable and hydrophilic.Motif analysis revealed that,apart from the AP2/ERF domain,other conserved regions were selec-tively distributed among different clades of the phylogenetic tree.Cis-acting element analysis showed that the promoter regions of the AP2/ERF family genes were significantly enriched in regulatory ele-ments associated with light response,plant hormone signal transduction,and abiotic stress responses.Chromosomal localization results indicated that the AP2/ERF genes were unevenly distributed across eight chromosomes.Intraspecific collinearity analysis revealed 71 collinear gene pairs among the AP2/ERF genes.Interspecific collinearity analysis showed that the SdAP2/ERF genes were evolutionarily closer to the homologous genes of Daucus carota L.Transcriptome analysis demonstrated that,com-pared with BC provenance of Saposhnikovia divaricata,significantly differentially expressed genes were observed in the CC provenance,with SdERF08,SdERF07,SdERF09 and SdERF28 showing significantly high expression,which could be closely associated with the growth characteristics of Sa-poshnikovia diuaricata.
崔喜嘉;范茹萱;林红梅;孙卓;于静静;杨利民;王云贺;韩忠明
吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118青岛恒星科技学院,山东青岛 266100吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118吉林农业大学中药材学院/吉林省药用植物生态种植重点试验室/省部共建生态恢复和生态系统管理国家重点实验室培育基地,长春 130118||吉林吉隆东北沙棘产业有限责任公司,吉林大安 131300
农业科技
防风AP2/ERF转录因子生物信息学分析系统发育表达模式
Saposhnikovia divaricataAP2/ERF transcription factorbioinformatics analysisphylogenyexpression pattern
《种子》 2026 (8)
60-70,11
吉林省科技厅重点研发项目(20260204099YY20260204045YY)中央财政林业科技推广示范项目(JLT2026-30)
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