{"title":"NAC转录因子LpNAC48促进百合毛状体的形成","authors":"Yin Xin, Wenqiang Pan, Yajie Zhao, Chenglong Yang, Jingru Li, Shaokun Wang, Jingxiang Wu, Mingfang Zhang, Jinxin Shi, Yang Ma, Shaozhong Fang, Yuwei Liang, Michele Zaccai, Xiuhai Zhang, Yunpeng Du, Jian Wu","doi":"10.1093/plphys/kiaf001","DOIUrl":null,"url":null,"abstract":"Trichomes play a crucial role in plant resistance to abiotic and biotic stresses, and their development and characteristics vary across different species. This study demonstrates that trichomes of Lilium pumilum exhibit synchronized growth during flower bud differentiation and enhance the plant's adaptability to UV-B radiation and aphid infection. We identified LpNAC48, a NAC family transcription factor (TF), that interacted with the B-box (BBX) family TF LpBBX28, during trichome formation in L. pumilum. Silencing LpNAC48 or LpBBX28 impaired trichome development and reduced trichome density on the outer perianths. We demonstrated that the upstream regulators LpNAC48 and LpBBX28 directly bound to the promoter of the bHLH TF-encoding gene LpGL3-LIKE (LpGL3L) to activate its expression. Moreover, an ABA-responsive element within a 259-bp DNA variation in the LpNAC48 promoter was important for its expression and was bound by the bZIP TF LpbZIP29 during trichome development. This binding activated LpNAC48 expression and contributed to trichome formation. This study provides insights into the role of a small DNA sequence variation in gene expression and trichome traits.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"14 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The NAC transcription factor LpNAC48 promotes trichome formation in Lilium pumilum\",\"authors\":\"Yin Xin, Wenqiang Pan, Yajie Zhao, Chenglong Yang, Jingru Li, Shaokun Wang, Jingxiang Wu, Mingfang Zhang, Jinxin Shi, Yang Ma, Shaozhong Fang, Yuwei Liang, Michele Zaccai, Xiuhai Zhang, Yunpeng Du, Jian Wu\",\"doi\":\"10.1093/plphys/kiaf001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Trichomes play a crucial role in plant resistance to abiotic and biotic stresses, and their development and characteristics vary across different species. This study demonstrates that trichomes of Lilium pumilum exhibit synchronized growth during flower bud differentiation and enhance the plant's adaptability to UV-B radiation and aphid infection. We identified LpNAC48, a NAC family transcription factor (TF), that interacted with the B-box (BBX) family TF LpBBX28, during trichome formation in L. pumilum. Silencing LpNAC48 or LpBBX28 impaired trichome development and reduced trichome density on the outer perianths. We demonstrated that the upstream regulators LpNAC48 and LpBBX28 directly bound to the promoter of the bHLH TF-encoding gene LpGL3-LIKE (LpGL3L) to activate its expression. Moreover, an ABA-responsive element within a 259-bp DNA variation in the LpNAC48 promoter was important for its expression and was bound by the bZIP TF LpbZIP29 during trichome development. This binding activated LpNAC48 expression and contributed to trichome formation. This study provides insights into the role of a small DNA sequence variation in gene expression and trichome traits.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"14 1\",\"pages\":\"\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2025-01-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/plphys/kiaf001\",\"RegionNum\":1,\"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":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf001","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The NAC transcription factor LpNAC48 promotes trichome formation in Lilium pumilum
Trichomes play a crucial role in plant resistance to abiotic and biotic stresses, and their development and characteristics vary across different species. This study demonstrates that trichomes of Lilium pumilum exhibit synchronized growth during flower bud differentiation and enhance the plant's adaptability to UV-B radiation and aphid infection. We identified LpNAC48, a NAC family transcription factor (TF), that interacted with the B-box (BBX) family TF LpBBX28, during trichome formation in L. pumilum. Silencing LpNAC48 or LpBBX28 impaired trichome development and reduced trichome density on the outer perianths. We demonstrated that the upstream regulators LpNAC48 and LpBBX28 directly bound to the promoter of the bHLH TF-encoding gene LpGL3-LIKE (LpGL3L) to activate its expression. Moreover, an ABA-responsive element within a 259-bp DNA variation in the LpNAC48 promoter was important for its expression and was bound by the bZIP TF LpbZIP29 during trichome development. This binding activated LpNAC48 expression and contributed to trichome formation. This study provides insights into the role of a small DNA sequence variation in gene expression and trichome traits.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.