Identification of a central regulator of ginkgolide biosynthesis in Ginkgo biloba that integrates jasmonate and light signaling

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2025-02-04 DOI:10.1073/pnas.2408891122
Jinfa Du, Zhen Zhao, Lingqi Jin, Lijin Huang, Dian Jin, Xiaoyan Zheng, Qiaolei Wang, Wenbo Xu, Huijun Guo, Xinyue Xing, Raphael N. Alolga, Lam-Son Phan Tran, Luis Rafael Herrera-Estrella, Ping Li, Xiaojian Yin, Xu Lu
{"title":"Identification of a central regulator of ginkgolide biosynthesis in Ginkgo biloba that integrates jasmonate and light signaling","authors":"Jinfa Du, Zhen Zhao, Lingqi Jin, Lijin Huang, Dian Jin, Xiaoyan Zheng, Qiaolei Wang, Wenbo Xu, Huijun Guo, Xinyue Xing, Raphael N. Alolga, Lam-Son Phan Tran, Luis Rafael Herrera-Estrella, Ping Li, Xiaojian Yin, Xu Lu","doi":"10.1073/pnas.2408891122","DOIUrl":null,"url":null,"abstract":"Ginkgolides are secondary metabolites unique to <jats:italic>Ginkgo biloba</jats:italic> with the potential to prevent and treat cardiovascular and cerebrovascular diseases. Although the biosynthetic pathways of ginkgolides have been partly uncovered, the mechanism regulating their biosynthesis is still largely unknown. Here, using multiomic and genetic analyses, we report the identification of a transcription factor, named ETHYLENE RESPONSE FACTOR ASSOCIATED WITH GINKGOLIDE BIOSYNTHESIS (GbEAG), as a critical regulator of ginkgolide biosynthesis. <jats:italic>GbEAG</jats:italic> is highly expressed in the roots of <jats:italic>G. biloba,</jats:italic> and its expression is significantly induced by methyl jasmonate (MeJA). Ginkgolide content was significantly increased in roots by overexpressing <jats:italic>GbEAG</jats:italic> using a “cut-dip-regeneration” system. GbEAG positively regulates ginkgolide biosynthesis by directly binding to the GCC-boxes in the promoter regions of genes involved in the biosynthesis of ginkgolides, such as <jats:italic>ISOPENTENYL DIPHOSPHATE ISOMERASE</jats:italic> ( <jats:italic>GbIDI</jats:italic> ) and <jats:italic>CYTOCHROME P450 7005C3</jats:italic> ( <jats:italic>GbCYP7005C3</jats:italic> ). GbEAG mediates the jasmonic acid (JA)-activated ginkgolide synthesis through its direct interaction with the JASMONATE ZINC-FINGER INFLORESCENCE MERISTEM DOMAIN 3 (GbJAZ3) repressor. Importantly, we also found that the central light-response regulator ELONGATED HYPOCOTYL 5 (GbHY5) mediates light induction of ginkgolide biosynthesis by binding to the G-box in the <jats:italic>GbEAG</jats:italic> promoter. Our findings provide mechanistic insights into the coordinated regulation of ginkgolide biosynthesis via JA and light signals, with GbEAG as a central regulator in <jats:italic>G. biloba,</jats:italic> and shed light on the potential to develop ginkgolide-rich varieties through molecular breeding and gene editing.","PeriodicalId":20548,"journal":{"name":"Proceedings of the National Academy of Sciences of the United States of America","volume":"9 1","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2025-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the National Academy of Sciences of the United States of America","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1073/pnas.2408891122","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Ginkgolides are secondary metabolites unique to Ginkgo biloba with the potential to prevent and treat cardiovascular and cerebrovascular diseases. Although the biosynthetic pathways of ginkgolides have been partly uncovered, the mechanism regulating their biosynthesis is still largely unknown. Here, using multiomic and genetic analyses, we report the identification of a transcription factor, named ETHYLENE RESPONSE FACTOR ASSOCIATED WITH GINKGOLIDE BIOSYNTHESIS (GbEAG), as a critical regulator of ginkgolide biosynthesis. GbEAG is highly expressed in the roots of G. biloba, and its expression is significantly induced by methyl jasmonate (MeJA). Ginkgolide content was significantly increased in roots by overexpressing GbEAG using a “cut-dip-regeneration” system. GbEAG positively regulates ginkgolide biosynthesis by directly binding to the GCC-boxes in the promoter regions of genes involved in the biosynthesis of ginkgolides, such as ISOPENTENYL DIPHOSPHATE ISOMERASE ( GbIDI ) and CYTOCHROME P450 7005C3 ( GbCYP7005C3 ). GbEAG mediates the jasmonic acid (JA)-activated ginkgolide synthesis through its direct interaction with the JASMONATE ZINC-FINGER INFLORESCENCE MERISTEM DOMAIN 3 (GbJAZ3) repressor. Importantly, we also found that the central light-response regulator ELONGATED HYPOCOTYL 5 (GbHY5) mediates light induction of ginkgolide biosynthesis by binding to the G-box in the GbEAG promoter. Our findings provide mechanistic insights into the coordinated regulation of ginkgolide biosynthesis via JA and light signals, with GbEAG as a central regulator in G. biloba, and shed light on the potential to develop ginkgolide-rich varieties through molecular breeding and gene editing.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
银杏中银杏内酯生物合成的一个整合茉莉酸和光信号的中央调控因子的鉴定
银杏内酯是银杏特有的次生代谢产物,具有预防和治疗心脑血管疾病的作用。虽然银杏内酯的生物合成途径已被部分揭示,但调控其生物合成的机制仍在很大程度上未知。通过多组学和遗传分析,我们发现了银杏内酯生物合成相关的乙烯反应因子(GbEAG),它是银杏内酯生物合成的关键调控因子。GbEAG在枇杷根中高表达,茉莉酸甲酯(MeJA)能显著诱导其表达。通过“切-浸-再生”体系过表达GbEAG,可显著提高根中银杏内酯含量。GbEAG通过直接结合参与银杏内酯生物合成的基因启动子区域的gcc -box,如异戊烯基二磷酸异构酶(GbIDI)和细胞色素P450 7005C3 (GbCYP7005C3),正向调节银杏内酯的生物合成。GbEAG通过直接与JASMONATE锌指花序分生系统结构域3 (GbJAZ3)抑制因子相互作用介导茉莉酸(JA)激活的银杏内酯合成。重要的是,我们还发现中枢光反应调节因子细长下胚轴5 (GbHY5)通过结合GbEAG启动子中的G-box介导银杏内酯生物合成的光诱导。我们的研究结果为银杏内酯生物合成通过JA和光信号协调调节的机制提供了见解,GbEAG是银杏内酯生物合成的中心调节因子,并揭示了通过分子育种和基因编辑开发富含银杏内酯品种的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
期刊最新文献
Inhibition of coronaviral exoribonuclease activity by TRIM-mediated SUMOylation. A mitochondrial-neuroinflammation-D-serine connection in epilepsy. Using wavelet decomposition to determine the dimension of structures from projected images. Endogenous ATP–powered nanomotors directing neural stem cell differentiation for Parkinson’s disease treatment HairTime: A noninvasive assay for estimating circadian phase from a single hair sample
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1