Alice Berhin, Aldana Ramirez, Manon Peeters, Gabriel Walckiers, Maxime Vannieuwenhuyze, Sylvain Legay, Belkacem El Amraoui, Charles Hachez
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Through comprehensive RNA-seq analysis of transgenic tobacco seedlings where long-stalked glandular trichome development was induced in aerial parts, we identified a suite of differentially expressed genes, including several transcription factors, shedding light on the early transcriptional cascade governing this developmental process. Moreover, through confocal live cell imaging of transcriptional reporter lines, interaction studies and DAP-seq assays, we confirmed the involvement of NtZFP8, a gene identified in our study, in long-stalked glandular trichome development. Our findings support a model in which NtZFP8 regulates a gene network essential for this developmental process. This study underscores the effectiveness of our approach in decoding the regulatory landscape of glandular trichome development in N. tabacum and provides a valuable framework for future functional investigations.</p>","PeriodicalId":20177,"journal":{"name":"Planta","volume":"262 6","pages":"123"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12528321/pdf/","citationCount":"0","resultStr":"{\"title\":\"Insight into the genetic network governing long-stalked glandular trichome development in Nicotiana tabacum.\",\"authors\":\"Alice Berhin, Aldana Ramirez, Manon Peeters, Gabriel Walckiers, Maxime Vannieuwenhuyze, Sylvain Legay, Belkacem El Amraoui, Charles Hachez\",\"doi\":\"10.1007/s00425-025-04840-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Main conclusion: </strong>Using a transcriptional switch-based approach in Nicotiana tabacum, we identified key regulatory factors that control long-stalked trichome development. Our results highlight candidate genes implicated in glandular trichome formation and establish a foundation for future research on trichome development. Glandular trichomes play a pivotal role in plant defense against various biotic and abiotic stresses. To unravel the genetic network driving glandular trichome development in Nicotiana tabacum, we employed a transcriptional switch-based approach using heterologous expression of AmMIXTA, a MYB transcription factor from Antirrhinum majus. Through comprehensive RNA-seq analysis of transgenic tobacco seedlings where long-stalked glandular trichome development was induced in aerial parts, we identified a suite of differentially expressed genes, including several transcription factors, shedding light on the early transcriptional cascade governing this developmental process. Moreover, through confocal live cell imaging of transcriptional reporter lines, interaction studies and DAP-seq assays, we confirmed the involvement of NtZFP8, a gene identified in our study, in long-stalked glandular trichome development. Our findings support a model in which NtZFP8 regulates a gene network essential for this developmental process. This study underscores the effectiveness of our approach in decoding the regulatory landscape of glandular trichome development in N. tabacum and provides a valuable framework for future functional investigations.</p>\",\"PeriodicalId\":20177,\"journal\":{\"name\":\"Planta\",\"volume\":\"262 6\",\"pages\":\"123\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12528321/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Planta\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s00425-025-04840-9\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Planta","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00425-025-04840-9","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Insight into the genetic network governing long-stalked glandular trichome development in Nicotiana tabacum.
Main conclusion: Using a transcriptional switch-based approach in Nicotiana tabacum, we identified key regulatory factors that control long-stalked trichome development. Our results highlight candidate genes implicated in glandular trichome formation and establish a foundation for future research on trichome development. Glandular trichomes play a pivotal role in plant defense against various biotic and abiotic stresses. To unravel the genetic network driving glandular trichome development in Nicotiana tabacum, we employed a transcriptional switch-based approach using heterologous expression of AmMIXTA, a MYB transcription factor from Antirrhinum majus. Through comprehensive RNA-seq analysis of transgenic tobacco seedlings where long-stalked glandular trichome development was induced in aerial parts, we identified a suite of differentially expressed genes, including several transcription factors, shedding light on the early transcriptional cascade governing this developmental process. Moreover, through confocal live cell imaging of transcriptional reporter lines, interaction studies and DAP-seq assays, we confirmed the involvement of NtZFP8, a gene identified in our study, in long-stalked glandular trichome development. Our findings support a model in which NtZFP8 regulates a gene network essential for this developmental process. This study underscores the effectiveness of our approach in decoding the regulatory landscape of glandular trichome development in N. tabacum and provides a valuable framework for future functional investigations.
期刊介绍:
Planta publishes timely and substantial articles on all aspects of plant biology.
We welcome original research papers on any plant species. Areas of interest include biochemistry, bioenergy, biotechnology, cell biology, development, ecological and environmental physiology, growth, metabolism, morphogenesis, molecular biology, new methods, physiology, plant-microbe interactions, structural biology, and systems biology.