Jinyuan Hu, Zishi Wang, He Xu, Zhenlong Wang, Ning Li, Rui Feng, Jianyu Yin, Fangru Liu, Baishi Wang
{"title":"野生大麻的转录组学分析:对组织和阶段特异性表达和次级代谢调节的见解。","authors":"Jinyuan Hu, Zishi Wang, He Xu, Zhenlong Wang, Ning Li, Rui Feng, Jianyu Yin, Fangru Liu, Baishi Wang","doi":"10.1186/s12864-025-11697-5","DOIUrl":null,"url":null,"abstract":"<p><p>Cannabis sativa is a medicinally and economically significant plant known for its production of cannabinoids, terpenoids, and other secondary metabolites. This study presents a transcriptomic analysis to elucidate tissue-specific expression and regulatory mechanisms across leaves, stems, and roots. A total of 2,530 differentially expressed genes (DEGs) were identified, with key genes such as terpene synthase (TPS) and phenylalanine ammonia-lyase (PAL) exhibiting elevated expression in leaf tissues, emphasizing their roles in terpenoid and phenylpropanoid biosynthesis. Alternative splicing (AS) analysis revealed 8,729 distinct events, dominated by exon skipping, contributing to transcriptomic diversity. Long non-coding RNA (lncRNA) prediction identified 3,245 candidates, many of which displayed tissue-specific expression patterns and co-expression with metabolic genes, suggesting regulatory roles in secondary metabolism. Additionally, 12,314 SNPs and 2,786 INDELs were detected, with notable enrichment in genes associated with secondary metabolite biosynthesis, particularly in leaf tissues. These findings advance the understanding of molecular mechanisms governing secondary metabolism and genetic diversity in C. sativa, providing valuable insights for future metabolic engineering and breeding strategies to enhance cannabinoid production.</p>","PeriodicalId":9030,"journal":{"name":"BMC Genomics","volume":"26 1","pages":"528"},"PeriodicalIF":3.5000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcriptomic analysis of wild Cannabis sativa: insights into tissue- and stage-specific expression and secondary metabolic regulation.\",\"authors\":\"Jinyuan Hu, Zishi Wang, He Xu, Zhenlong Wang, Ning Li, Rui Feng, Jianyu Yin, Fangru Liu, Baishi Wang\",\"doi\":\"10.1186/s12864-025-11697-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cannabis sativa is a medicinally and economically significant plant known for its production of cannabinoids, terpenoids, and other secondary metabolites. This study presents a transcriptomic analysis to elucidate tissue-specific expression and regulatory mechanisms across leaves, stems, and roots. A total of 2,530 differentially expressed genes (DEGs) were identified, with key genes such as terpene synthase (TPS) and phenylalanine ammonia-lyase (PAL) exhibiting elevated expression in leaf tissues, emphasizing their roles in terpenoid and phenylpropanoid biosynthesis. Alternative splicing (AS) analysis revealed 8,729 distinct events, dominated by exon skipping, contributing to transcriptomic diversity. Long non-coding RNA (lncRNA) prediction identified 3,245 candidates, many of which displayed tissue-specific expression patterns and co-expression with metabolic genes, suggesting regulatory roles in secondary metabolism. Additionally, 12,314 SNPs and 2,786 INDELs were detected, with notable enrichment in genes associated with secondary metabolite biosynthesis, particularly in leaf tissues. These findings advance the understanding of molecular mechanisms governing secondary metabolism and genetic diversity in C. sativa, providing valuable insights for future metabolic engineering and breeding strategies to enhance cannabinoid production.</p>\",\"PeriodicalId\":9030,\"journal\":{\"name\":\"BMC Genomics\",\"volume\":\"26 1\",\"pages\":\"528\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-05-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Genomics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s12864-025-11697-5\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12864-025-11697-5","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Transcriptomic analysis of wild Cannabis sativa: insights into tissue- and stage-specific expression and secondary metabolic regulation.
Cannabis sativa is a medicinally and economically significant plant known for its production of cannabinoids, terpenoids, and other secondary metabolites. This study presents a transcriptomic analysis to elucidate tissue-specific expression and regulatory mechanisms across leaves, stems, and roots. A total of 2,530 differentially expressed genes (DEGs) were identified, with key genes such as terpene synthase (TPS) and phenylalanine ammonia-lyase (PAL) exhibiting elevated expression in leaf tissues, emphasizing their roles in terpenoid and phenylpropanoid biosynthesis. Alternative splicing (AS) analysis revealed 8,729 distinct events, dominated by exon skipping, contributing to transcriptomic diversity. Long non-coding RNA (lncRNA) prediction identified 3,245 candidates, many of which displayed tissue-specific expression patterns and co-expression with metabolic genes, suggesting regulatory roles in secondary metabolism. Additionally, 12,314 SNPs and 2,786 INDELs were detected, with notable enrichment in genes associated with secondary metabolite biosynthesis, particularly in leaf tissues. These findings advance the understanding of molecular mechanisms governing secondary metabolism and genetic diversity in C. sativa, providing valuable insights for future metabolic engineering and breeding strategies to enhance cannabinoid production.
期刊介绍:
BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics.
BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.