Huang Juan, Wang Luyuan, Tang Bin, Ren Rongrong, Shi Taoxiong, Zhu Liwei, Deng Jiao, Liang Chenggang, Wang Yan, Chen Qingfu
Research Center of Buckwheat Industry Technology, Guizhou Normal University, Guiyang, China.
Tunliu District Vocational Senior Middle School, Changzhi, China.
Front Plant Sci. 2022 Jun 17;13:803472. doi: 10.3389/fpls.2022.803472. eCollection 2022.
Golden buckwheat () is used in Traditional Chinese Medicine. It has received attention because of the high value of its various medicinal and nutritional metabolites, especially flavonoids (catechin and epicatechin). However, the metabolites and their encoding genes in golden buckwheat have not yet been identified in the global landscape. This study performed transcriptomics and widely targeted metabolomics analyses for the first time on rhizomes of golden buckwheat. As a result, 10,191 differentially expressed genes (DEGs) and 297 differentially regulated metabolites (DRMs) were identified, among which the flavonoid biosynthesis pathway was enriched in both transcriptome and metabolome. The integration analyses of the transcriptome and the metabolome revealed a network related to catechin, in which four metabolites and 14 genes interacted with each other. Subsequently, an SG5 R2R3-MYB transcription factor, named , was identified as a transcriptional activator in catechin biosynthesis, as it was positively correlated to eight flavonoid biosynthesis genes in their expression patterns and was directly bound to the promoters of and by yeast one hybrid analysis. Finally, a flavonoid biosynthesis pathway was proposed in the rhizomes of golden buckwheat, including 13 metabolites, 11 genes encoding 9 enzymes, and 1 MYB transcription factor. The expression of 12 DEGs were validated by qRT-PCR, resulting in a good agreement with the Pearson R ranging from 0.83 to 1. The study provided a comprehensive flavonoid biosynthesis and regulatory network of golden buckwheat.
金荞麦()被用于传统中药。由于其各种药用和营养代谢产物,特别是黄酮类化合物(儿茶素和表儿茶素)具有很高的价值,它受到了关注。然而,金荞麦中的代谢产物及其编码基因在全球范围内尚未得到鉴定。本研究首次对金荞麦的根茎进行了转录组学和广泛靶向代谢组学分析。结果,鉴定出10191个差异表达基因(DEG)和297个差异调节代谢物(DRM),其中黄酮类生物合成途径在转录组和代谢组中均有富集。转录组和代谢组的整合分析揭示了一个与儿茶素相关的网络,其中四种代谢物和14个基因相互作用。随后,一个名为的SG5 R2R3-MYB转录因子被鉴定为儿茶素生物合成中的转录激活因子,因为它在表达模式上与八个黄酮类生物合成基因呈正相关,并且通过酵母单杂交分析直接与和的启动子结合。最后,提出了金荞麦根茎中的黄酮类生物合成途径,包括13种代谢物、11个编码9种酶的基因和1个MYB转录因子。通过qRT-PCR验证了12个DEG的表达,与Pearson R的相关性良好,范围为0.83至1。该研究提供了金荞麦全面的黄酮类生物合成和调控网络。