Jun Xiang, Xue Gong, Qianqian Fang, Liping Ding, Yinyi Zhang, Sujuan Xu, Ting Li, Man He, Ze Wu, Nianjun Teng
{"title":"乙烯响应因子LlERF092与LlETO1协同通过激活LlMBF1c提高百合的耐热性","authors":"Jun Xiang, Xue Gong, Qianqian Fang, Liping Ding, Yinyi Zhang, Sujuan Xu, Ting Li, Man He, Ze Wu, Nianjun Teng","doi":"10.1111/pbi.70269","DOIUrl":null,"url":null,"abstract":"Multiprotein bridging factor 1c (MBF1c) has been shown to play a critical role in plant responses to heat stress. Previous studies have implicated MBF1c roles in ethylene‐mediated thermotolerance; however, the upstream regulatory mechanisms linking MBF1c to this process remain unclear. In this study, an ethylene‐response factor (ERF), LlERF092, was identified as a potential regulator of <jats:italic>LlMBF1c</jats:italic> through a yeast one‐hybrid screening assay. Further investigations revealed that LlERF092 directly bound to the promoter of <jats:italic>LlMBF1c</jats:italic> and activated its transcription. <jats:italic>LlERF092</jats:italic> was rapidly induced by heat stress, and its protein localised to the nucleus. Overexpression of <jats:italic>LlERF092</jats:italic> enhanced the thermotolerance of the transgenic lily plants. Furthermore, immunoprecipitation followed by mass spectrometry (IP‐MS) identified LlETO1 (ETHYLENE OVERPRODUCER 1) as an interacting partner of LlERF092. The expression of <jats:italic>LlETO1</jats:italic> was activated in response to transient heat stress, and the LlETO1‐LlERF092 interaction enhanced the transcriptional activity of LlERF092. Co‐overexpression of <jats:italic>LlERF092</jats:italic> and <jats:italic>LlETO1</jats:italic> enhanced thermotolerance more than the overexpression of either gene alone, while co‐silencing of <jats:italic>LlERF092</jats:italic> and <jats:italic>LlETO1</jats:italic> further reduced thermotolerance compared to silencing each gene individually. Additionally, heat stress promoted ethylene production in lily leaves, and exogenous application of ethephon enhanced thermotolerance. Ethephon treatment also elevated the expression of <jats:italic>LlERF092</jats:italic>, <jats:italic>LlETO1</jats:italic>, and <jats:italic>LlMBF1c</jats:italic>, while their expression was repressed by 1‐MCP under heat stress. In summary, these findings demonstrated that the LlERF092/LlETO1‐LlMBF1c transcriptional cascade mediated ethylene‐dependent thermotolerance in lily under heat stress conditions. This study provides new insights into the molecular mechanisms underlying plant heat stress responses and highlights the role of ethylene signalling in thermotolerance.","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"12 1","pages":""},"PeriodicalIF":10.5000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An Ethylene‐Response Factor LlERF092 Coordinates With LlETO1 to Improve Thermotolerance by Activating LlMBF1c in Lily\",\"authors\":\"Jun Xiang, Xue Gong, Qianqian Fang, Liping Ding, Yinyi Zhang, Sujuan Xu, Ting Li, Man He, Ze Wu, Nianjun Teng\",\"doi\":\"10.1111/pbi.70269\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Multiprotein bridging factor 1c (MBF1c) has been shown to play a critical role in plant responses to heat stress. Previous studies have implicated MBF1c roles in ethylene‐mediated thermotolerance; however, the upstream regulatory mechanisms linking MBF1c to this process remain unclear. In this study, an ethylene‐response factor (ERF), LlERF092, was identified as a potential regulator of <jats:italic>LlMBF1c</jats:italic> through a yeast one‐hybrid screening assay. Further investigations revealed that LlERF092 directly bound to the promoter of <jats:italic>LlMBF1c</jats:italic> and activated its transcription. <jats:italic>LlERF092</jats:italic> was rapidly induced by heat stress, and its protein localised to the nucleus. Overexpression of <jats:italic>LlERF092</jats:italic> enhanced the thermotolerance of the transgenic lily plants. Furthermore, immunoprecipitation followed by mass spectrometry (IP‐MS) identified LlETO1 (ETHYLENE OVERPRODUCER 1) as an interacting partner of LlERF092. The expression of <jats:italic>LlETO1</jats:italic> was activated in response to transient heat stress, and the LlETO1‐LlERF092 interaction enhanced the transcriptional activity of LlERF092. Co‐overexpression of <jats:italic>LlERF092</jats:italic> and <jats:italic>LlETO1</jats:italic> enhanced thermotolerance more than the overexpression of either gene alone, while co‐silencing of <jats:italic>LlERF092</jats:italic> and <jats:italic>LlETO1</jats:italic> further reduced thermotolerance compared to silencing each gene individually. Additionally, heat stress promoted ethylene production in lily leaves, and exogenous application of ethephon enhanced thermotolerance. Ethephon treatment also elevated the expression of <jats:italic>LlERF092</jats:italic>, <jats:italic>LlETO1</jats:italic>, and <jats:italic>LlMBF1c</jats:italic>, while their expression was repressed by 1‐MCP under heat stress. In summary, these findings demonstrated that the LlERF092/LlETO1‐LlMBF1c transcriptional cascade mediated ethylene‐dependent thermotolerance in lily under heat stress conditions. This study provides new insights into the molecular mechanisms underlying plant heat stress responses and highlights the role of ethylene signalling in thermotolerance.\",\"PeriodicalId\":221,\"journal\":{\"name\":\"Plant Biotechnology Journal\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":10.5000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Biotechnology Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1111/pbi.70269\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/pbi.70269","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
An Ethylene‐Response Factor LlERF092 Coordinates With LlETO1 to Improve Thermotolerance by Activating LlMBF1c in Lily
Multiprotein bridging factor 1c (MBF1c) has been shown to play a critical role in plant responses to heat stress. Previous studies have implicated MBF1c roles in ethylene‐mediated thermotolerance; however, the upstream regulatory mechanisms linking MBF1c to this process remain unclear. In this study, an ethylene‐response factor (ERF), LlERF092, was identified as a potential regulator of LlMBF1c through a yeast one‐hybrid screening assay. Further investigations revealed that LlERF092 directly bound to the promoter of LlMBF1c and activated its transcription. LlERF092 was rapidly induced by heat stress, and its protein localised to the nucleus. Overexpression of LlERF092 enhanced the thermotolerance of the transgenic lily plants. Furthermore, immunoprecipitation followed by mass spectrometry (IP‐MS) identified LlETO1 (ETHYLENE OVERPRODUCER 1) as an interacting partner of LlERF092. The expression of LlETO1 was activated in response to transient heat stress, and the LlETO1‐LlERF092 interaction enhanced the transcriptional activity of LlERF092. Co‐overexpression of LlERF092 and LlETO1 enhanced thermotolerance more than the overexpression of either gene alone, while co‐silencing of LlERF092 and LlETO1 further reduced thermotolerance compared to silencing each gene individually. Additionally, heat stress promoted ethylene production in lily leaves, and exogenous application of ethephon enhanced thermotolerance. Ethephon treatment also elevated the expression of LlERF092, LlETO1, and LlMBF1c, while their expression was repressed by 1‐MCP under heat stress. In summary, these findings demonstrated that the LlERF092/LlETO1‐LlMBF1c transcriptional cascade mediated ethylene‐dependent thermotolerance in lily under heat stress conditions. This study provides new insights into the molecular mechanisms underlying plant heat stress responses and highlights the role of ethylene signalling in thermotolerance.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.