Liu Sizhang, Chen Xiaxia, Zhao Tianqi, Yu Jinghui, Chen Ping, Wang Yanfang, Wang Kangyu, Zhao Mingzhu, Jiang Yue, Wang Yi, Zhang Meiping
College of Life Science, Jilin Agricultural University, Changchun 130118, China.
Research Center for Ginseng Genetic Resources Development and Utilization, Jilin Province, Jilin Agricultural University, Changchun 130118, China.
Plants (Basel). 2024 Jun 27;13(13):1784. doi: 10.3390/plants13131784.
Ginseng, an important medicinal plant, is characterized by its main active component, ginsenosides. Among more than 40 ginsenosides, Rg1 is one of the ginsenosides used for measuring the quality of ginseng. Therefore, the identification and characterization of genes for Rg1 biosynthesis are important to elucidate the molecular basis of Rg1 biosynthesis. In this study, we utilized 39,327 SNPs and the corresponding Rg1 content from 344 core ginseng cultivars from Jilin Province. We conducted a genome-wide association study (GWAS) combining weighted gene co-expression network analysis (WGCNA), SNP-Rg1 content association analysis, and gene co-expression network analysis; three candidate Rg1 genes (, , and ) and one crucial candidate gene () were identified. Functional validation of was performed using methyl jasmonate (MeJA) regulation and RNAi, confirming that this gene regulates Rg1 biosynthesis. The spatial-temporal expression patterns of the gene and known key enzyme genes involved in ginsenoside biosynthesis differ. Furthermore, variations in their networks have a significant impact on Rg1 biosynthesis. This study established an accurate and efficient method for identifying candidate genes, cloned a novel gene controlling Rg1 biosynthesis, and identified 73 SNPs significantly associated with Rg1 content. This provides genetic resources and effective tools for further exploring the molecular mechanisms of Rg1 biosynthesis and molecular breeding.
人参是一种重要的药用植物,其主要活性成分为人参皂苷。在40多种人参皂苷中,Rg1是用于衡量人参质量的人参皂苷之一。因此,鉴定和表征Rg1生物合成相关基因对于阐明Rg1生物合成的分子基础具有重要意义。在本研究中,我们利用了来自吉林省344个核心人参品种的39327个单核苷酸多态性(SNP)以及相应的Rg1含量。我们进行了全基因组关联研究(GWAS),结合加权基因共表达网络分析(WGCNA)、SNP-Rg1含量关联分析和基因共表达网络分析;鉴定出了3个候选Rg1基因(、和)和1个关键候选基因()。使用茉莉酸甲酯(MeJA)调控和RNA干扰对进行了功能验证,证实该基因调控Rg1生物合成。该基因和参与人参皂苷生物合成的已知关键酶基因的时空表达模式不同。此外,它们网络中的变异对Rg1生物合成有显著影响。本研究建立了一种准确有效的候选基因鉴定方法,克隆了一个控制Rg1生物合成的新基因,并鉴定出73个与Rg1含量显著相关的SNP。这为进一步探索Rg1生物合成的分子机制和分子育种提供了遗传资源和有效工具。