{"title":"[Transcriptome sequencing reveals molecular mechanism of seed dormancy release of Zanthoxylum nitidum].","authors":"Chang-Qian Quan, Dan-Feng Tang, Jian-Ping Jiang, Yan-Xia Zhu","doi":"10.19540/j.cnki.cjcmm.20241014.103","DOIUrl":null,"url":null,"abstract":"<p><p>The transcriptome sequencing based on Illumina Novaseq 6000 Platform was performed with the untreated seed embryo(DS), stratified seed embryo(SS), and germinated seed embryo(GS) of Zanthoxylum nitidum, aiming to explore the molecular mechanism regulating the seed dormancy and germination of Z. nitidum and uncover key differentially expressed genes(DEGs). A total of 61.41 Gb clean data was obtained, and 86 386 unigenes with an average length of 773.49 bp were assembled. A total of 29 290 DEGs were screened from three comparison groups(SS vs DS, GS vs SS, and GS vs DS), and these genes were annotated on 134 Kyoto Encyclopedia of Genes and Genomes(KEGG) pathways. KEGG enrichment analysis revealed that the plant hormone signal transduction pathway is the richest pathway, containing 226 DEGs. Among all DEGs, 894 transcription factors were identified, which were distributed across 34 transcription factor families. These transcription factors were also mainly concentrated in plant hormone signal transduction and mitogen-activated protein kinase(MAPK) signaling pathways. Further real-time quantitative polymerase chain reaction(RT-qPCR) validation of 12 DEGs showed that the transcriptome data is reliable. During the process of seed dormancy release and germination, a large number of DEGs involved in polysaccharide degradation, protein synthesis, lipid metabolism, and hormone signal transduction were expressed. These genes were involved in multiple metabolic pathways, forming a complex regulatory network for dormancy and germination. This study lays a solid foundation for analyzing the molecular mechanisms of seed dormancy and germination of Z. nitidum.</p>","PeriodicalId":52437,"journal":{"name":"Zhongguo Zhongyao Zazhi","volume":"50 1","pages":"102-110"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhongguo Zhongyao Zazhi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19540/j.cnki.cjcmm.20241014.103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
The transcriptome sequencing based on Illumina Novaseq 6000 Platform was performed with the untreated seed embryo(DS), stratified seed embryo(SS), and germinated seed embryo(GS) of Zanthoxylum nitidum, aiming to explore the molecular mechanism regulating the seed dormancy and germination of Z. nitidum and uncover key differentially expressed genes(DEGs). A total of 61.41 Gb clean data was obtained, and 86 386 unigenes with an average length of 773.49 bp were assembled. A total of 29 290 DEGs were screened from three comparison groups(SS vs DS, GS vs SS, and GS vs DS), and these genes were annotated on 134 Kyoto Encyclopedia of Genes and Genomes(KEGG) pathways. KEGG enrichment analysis revealed that the plant hormone signal transduction pathway is the richest pathway, containing 226 DEGs. Among all DEGs, 894 transcription factors were identified, which were distributed across 34 transcription factor families. These transcription factors were also mainly concentrated in plant hormone signal transduction and mitogen-activated protein kinase(MAPK) signaling pathways. Further real-time quantitative polymerase chain reaction(RT-qPCR) validation of 12 DEGs showed that the transcriptome data is reliable. During the process of seed dormancy release and germination, a large number of DEGs involved in polysaccharide degradation, protein synthesis, lipid metabolism, and hormone signal transduction were expressed. These genes were involved in multiple metabolic pathways, forming a complex regulatory network for dormancy and germination. This study lays a solid foundation for analyzing the molecular mechanisms of seed dormancy and germination of Z. nitidum.
基于Illumina Novaseq 6000平台对nitidum花椒(Zanthoxylum nitidum)未处理种子胚(DS)、分层种子胚(SS)和萌发种子胚(GS)进行转录组测序,旨在探索nitidum种子休眠和萌发的分子调控机制,揭示关键差异表达基因(DEGs)。共获得61.41 Gb的clean数据,共组装了86 386个unigenes,平均长度为773.49 bp。从3个对照组(SS vs DS、GS vs SS和GS vs DS)中共筛选出29 290个基因,并在134条京都基因与基因组百科(KEGG)通路上进行了注释。KEGG富集分析表明,植物激素信号转导途径是最丰富的途径,含有226个deg。在所有deg中,鉴定出894个转录因子,分布在34个转录因子家族中。这些转录因子也主要集中在植物激素信号转导和丝裂原活化蛋白激酶(MAPK)信号通路中。进一步的实时定量聚合酶链反应(RT-qPCR)验证了12个基因的转录组数据是可靠的。在种子休眠释放和萌发过程中,大量参与多糖降解、蛋白质合成、脂质代谢和激素信号转导的deg表达。这些基因参与了多种代谢途径,形成了一个复杂的休眠和萌发调控网络。本研究为深入分析玉米种子休眠和萌发的分子机制奠定了坚实的基础。