乙烯响应因子LlERF12调控卷丹珠芽发生机制的初步解析OA北大核心
Preliminary analysis of the mechanism of ethylene response factor LIERF12 regulating bulbil formation in Lilium lancifolium
为探究乙烯(Ethylene)对卷丹珠芽发生的作用,以卷丹(Lilium lancifolium)为试验材料,利用不同浓度的乙烯利(Ethephon,ETH)和乙烯信号转导抑制剂1-甲基环丙烯(1-Methylcyclopropene,1-MCP)处理卷丹茎段,对其进行表型统计、生理指标测定和下游基因表达情况分析;通过卷丹珠芽形成过程的转录组数据筛选到可能参与调控珠芽发生的乙烯响应转录因子——LlE RF 12(Ethylene responsive factor 12),利用生物信息学软件对其生化特性分析预测;利用实时荧光定量法检测LlERF12基因在不同时期、不同组织、不同百合品种以及不同浓度ETH和1-MCP处理下的表达;最终通过基因沉默技术验证LlERF12在卷丹珠芽发生过程中的作用.结果表明:1)卷丹珠芽的发生发育过程共划分为4个时期:S0~S3;2)1-MCP处理导致叶腋处葡萄糖含量增加,通过促进腋芽发生标志基因LlSTM(SHOOTMERISTEMLESS)的表达量而促进卷丹珠芽的发生数量,而ETH处理则通过抑制LlSTM表达而抑制了珠芽发生数量;3)LlERF12在珠芽准备发生时期表达量较高,并且在自然能发生珠芽的百合品种中的表达量显著高于其他百合品种;4)ETH处理显著抑制LlERF12的表达,1-MCP处理则相反;5)沉默LlERF12基因导致LlSTM表达下降,进一步抑制了卷丹珠芽的发生数量,证明了 LlERF12在珠芽发生过程中的正调控作用.综上,LlERF12通过响应乙烯信号转导,促进叶腋处葡萄糖积累,影响下游腋芽发生标志基因LlSTM的表达,从而调控卷丹珠芽的形成.
To explore the effect of ethylene on bulbil formation of Lilium lancifolium,the stem segment of Lilium lancifolium was treated with different concentrations of ethephon(ETH)and ethylene signal transduction inhibitor 1-methylcyclopropene(1-MCP).The phenotypic statistics,physiological index determination and downstream gene expression analysis were carried out.The ethylene responsive factor LIERF12 that may be involved in the regulation of bulbil formation was screened by using transcriptome data of L.lancifolium bulbil formation process.Bioinformatics software was used to analyze and predict its biochemical characteristics.The expression of LIERF12 gene in different periods,different tissues,different lily varieties and different concentrations of ETH and 1-MCP treatment was detected by real-time fluorescence quantification.Finally,the role of LIERF12 in the process of bulbil formation of L.lancifolium was verified by VIGS technology.The results showed that:1)The development process of L.lancifolium bulbils was divided into four periods,which were S0,S1,S2,and S3;2)1-MCP treatment increased the glucose content in leaf axils and promoted the number of bulbils by promoting the expression of axillary bud marker gene LISTM(SHOOTMERISTEMLESS),while ETH treatment reduced the number of bulbils by inhibiting the expression of LISTM.3)The expression level of LIERF12 was higher in the period of bulbil preparation,and the expression level of LIERF12 in lily varieties with natural bulbils was significantly higher than in other lily varieties.4)ETH treatment significantly inhibited the expression of LIERF12,while 1-MCP treatment was the opposite.5)Silencing the LIERF12 gene resulted in a decrease in the expression of LISTM,which further inhibited the number of bulbils of L.lancifolium,demonstrating the positive regulatory role of LIERF12 in the process of bulbil formation.In summary,LIERF12 promotes the accumulation of glucose in leaf axils and affects the expression of the downstream axillary bud marker gene LISTM by responding to ethylene signal transduction,thereby regulating the formation of bulbils of L.lancifolium.
王梦迪;杜运鹏;梁佳惠;潘文强;马艳芳;金梦竹;张铭芳;杨凤萍;张秀海;于晓南
北京林业大学园林学院/花卉种质创新与分子育种北京市重点实验室,北京 100083||北京市农林科学院草业花卉与景观生态研究所/国家林业草原赏食百合工程技术研究中心,北京 100097北京市农林科学院草业花卉与景观生态研究所/国家林业草原赏食百合工程技术研究中心,北京 100097北京林业大学园林学院/花卉种质创新与分子育种北京市重点实验室,北京 100083
园艺学与植物营养学
卷丹珠芽LlERF12乙烯基因沉默
Lilium lancifoliumbulbil formationLIERF12ethylenegene silencing
《中国农业大学学报》 2025 (002)
80-93 / 14
国家自然科学基金项目(32171864,32371954);北京市农林科学院优秀青年基金项目(YXQN202303);北京市农林科学院国际科技合作平台建设项目(2024-13)
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