Combined Analysis of Transcriptome and Small RNA Sequencing Reveals the Mechanism of UV-B-promoted Flavonoid Biosynthesis in Ginkgo biloba

IF 1.1 4区 生物学 Q3 PLANT SCIENCES
Y. Chu, H. Zhang, P. Wan, W. Li, L. Wang, S. Liu
{"title":"Combined Analysis of Transcriptome and Small RNA Sequencing Reveals the Mechanism of UV-B-promoted Flavonoid Biosynthesis in Ginkgo biloba","authors":"Y. Chu, H. Zhang, P. Wan, W. Li, L. Wang, S. Liu","doi":"10.1134/s1021443724604749","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>Flavonoids are the most abundant medicinal ingredients in <i>Ginkgo biloba</i> L. leaf extract (GBE), which is an important industrial raw material for the treatment of cardiovascular and cerebrovascular diseases. Our previous study found significantly higher flavonoid content in <i>G.</i> <i>biloba</i> leaves treated with UV-B for 7 days. However, the molecular mechanisms by which the miRNA-mRNA network responds to UV-B irradiation and regulates flavonoid biosynthesis remain unclear. Here, we identified 1348 differentially expressed genes (DEGs) by transcriptome sequencing of <i>G.</i> <i>biloba</i> leaves from UV-B treatment at 0 (CK) and 7 days, and 89.76% of DEG were induced by UV-B irradiation. Analysis of the flavonoid biosynthesis pathway revealed 16 differentially expressed structural genes (SGs), all of which were upregulated after UV-B treatment. Twelve DEGs were identified by analyzing transcription factors (TFs), including MYB, bHLH, and WD40, which regulate flavonoid biosynthesis, 11 of which were upregulated. Furthermore, small RNA sequencing of ginkgo leaves from control and UV-B-treated groups on days 0 and 7 revealed 58 differentially expressed miRNAs (DEMs). KEGG enrichment analysis showed that the target genes of the DEMs were significantly enriched in the flavonoid biosynthesis pathway. Finally, combined analysis of transcriptome and miRNA data identified 32 DEMs targeting 43 SGs involved in flavonoid biosynthesis, and 42 DEMs targeting 68 TFs that regulate flavonoid biosynthesis. Taken together, our findings revealed that multiple miRNA-SG and miRNA-TF networks may regulate <i>G.</i> <i>biloba</i> flavonoid biosynthesis in response to UV-B irradiation, providing new insights into the miRNA regulation of <i>G.</i> <i>biloba</i> flavonoid biosynthesis.</p>","PeriodicalId":21477,"journal":{"name":"Russian Journal of Plant Physiology","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1134/s1021443724604749","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Flavonoids are the most abundant medicinal ingredients in Ginkgo biloba L. leaf extract (GBE), which is an important industrial raw material for the treatment of cardiovascular and cerebrovascular diseases. Our previous study found significantly higher flavonoid content in G. biloba leaves treated with UV-B for 7 days. However, the molecular mechanisms by which the miRNA-mRNA network responds to UV-B irradiation and regulates flavonoid biosynthesis remain unclear. Here, we identified 1348 differentially expressed genes (DEGs) by transcriptome sequencing of G. biloba leaves from UV-B treatment at 0 (CK) and 7 days, and 89.76% of DEG were induced by UV-B irradiation. Analysis of the flavonoid biosynthesis pathway revealed 16 differentially expressed structural genes (SGs), all of which were upregulated after UV-B treatment. Twelve DEGs were identified by analyzing transcription factors (TFs), including MYB, bHLH, and WD40, which regulate flavonoid biosynthesis, 11 of which were upregulated. Furthermore, small RNA sequencing of ginkgo leaves from control and UV-B-treated groups on days 0 and 7 revealed 58 differentially expressed miRNAs (DEMs). KEGG enrichment analysis showed that the target genes of the DEMs were significantly enriched in the flavonoid biosynthesis pathway. Finally, combined analysis of transcriptome and miRNA data identified 32 DEMs targeting 43 SGs involved in flavonoid biosynthesis, and 42 DEMs targeting 68 TFs that regulate flavonoid biosynthesis. Taken together, our findings revealed that multiple miRNA-SG and miRNA-TF networks may regulate G. biloba flavonoid biosynthesis in response to UV-B irradiation, providing new insights into the miRNA regulation of G. biloba flavonoid biosynthesis.

Abstract Image

转录组和小 RNA 测序联合分析揭示了紫外线-B 促进银杏叶类黄酮生物合成的机制
摘要类黄酮是银杏叶提取物(GBE)中最丰富的药用成分,是治疗心脑血管疾病的重要工业原料。我们之前的研究发现,经紫外线-B 处理 7 天的银杏叶中黄酮类化合物含量明显较高。然而,miRNA-mRNA 网络响应 UV-B 照射并调控类黄酮生物合成的分子机制仍不清楚。在此,我们通过转录组测序鉴定了1348个差异表达基因(DEGs),其中89.76%的DEGs由UV-B照射诱导。对黄酮类化合物生物合成途径的分析发现了 16 个差异表达的结构基因(SGs),这些基因在紫外线-B 处理后全部上调。通过分析转录因子(TFs),包括调控类黄酮生物合成的 MYB、bHLH 和 WD40,发现了 12 个 DEGs,其中 11 个上调。此外,对第0天和第7天对照组和紫外线-B处理组的银杏叶进行小RNA测序,发现了58个差异表达的miRNA(DEMs)。KEGG 富集分析表明,DEMs 的靶基因在类黄酮生物合成途径中明显富集。最后,通过对转录组和 miRNA 数据的综合分析,发现了 32 个以参与类黄酮生物合成的 43 个 SG 为靶基因的 DEMs,以及 42 个以调控类黄酮生物合成的 68 个 TF 为靶基因的 DEMs。总之,我们的研究结果揭示了多个 miRNA-SG 和 miRNA-TF 网络可能调控双叶植物黄酮类化合物的生物合成以应对 UV-B 照射,为 miRNA 调控双叶植物黄酮类化合物的生物合成提供了新的见解。
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 求助全文
来源期刊
CiteScore
4.00
自引率
14.30%
发文量
107
审稿时长
6 months
期刊介绍: Russian Journal of Plant Physiology is a leading journal in phytophysiology. It embraces the full spectrum of plant physiology and brings together the related aspects of biophysics, biochemistry, cytology, anatomy, genetics, etc. The journal publishes experimental and theoretical articles, reviews, short communications, and descriptions of new methods. Some issues cover special problems of plant physiology, thus presenting collections of articles and providing information in rapidly growing fields. The editorial board is highly interested in publishing research from all countries and accepts manuscripts in English.
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信