Integrated metabolome and transcriptome analyses reveal the role of BoGSTF12 in anthocyanin accumulation in Chinese kale (Brassica oleracea var. alboglabra)

花青素 生物 代谢组 转录组 氰化物 颜料 红卷心菜 芸苔属 甘蓝 拟南芥 植物 拟南芥 代谢组学 基因 突变体 园艺 生物化学 基因表达 生物信息学 化学 有机化学
作者
Kang Tang,Umer Karamat,Guihua Li,Juxian Guo,Shizheng Jiang,Mei Fu,Xian Yang
出处
期刊:BMC Plant Biology [BioMed Central]
卷期号:24 (1) 被引量:8
标识
DOI:10.1186/s12870-024-05016-5
摘要

Abstract Background The vivid red, purple, and blue hues that are observed in a variety of plant fruits, flowers, and leaves are produced by anthocyanins, which are naturally occurring pigments produced by a series of biochemical processes occurring inside the plant cells. The purple-stalked Chinese kale, a popular vegetable that contains anthocyanins, has many health benefits but needs to be investigated further to identify the genes involved in the anthocyanin biosynthesis and translocation in this vegetable. Results In this study, the purple- and green-stalked Chinese kale were examined using integrative transcriptome and metabolome analyses. The content of anthocyanins such as cyanidin-3- O -(6″- O -feruloyl) sophoroside-5- O -glucoside, cyanidin-3,5- O -diglucoside (cyanin), and cyanidin-3- O -(6″- O - p -hydroxybenzoyl) sophoroside-5- O -glucoside were considerably higher in purple-stalked Chinese kale than in its green-stalked relative. RNA-seq analysis indicated that 23 important anthocyanin biosynthesis genes, including 3 PAL , 2 C4H , 3 4CL , 3 CHS , 1 CHI , 1 F3H , 2 FLS , 2 F3’H , 1 DFR , 3 ANS , and 2 UFGT , along with the transcription factor BoMYB114 , were significantly differentially expressed between the purple- and green-stalked varieties. Results of analyzing the expression levels of 11 genes involved in anthocyanin production using qRT-PCR further supported our findings. Association analysis between genes and metabolites revealed a strong correlation between BoGSTF12 and anthocyanin. We overexpressed BoGSTF12 in Arabidopsis thaliana tt19 , an anthocyanin transport mutant, and this rescued the anthocyanin-loss phenotype in the stem and rosette leaves, indicating BoGSTF12 encodes an anthocyanin transporter that affects the accumulation of anthocyanins. Conclusion This work represents a key step forward in our understanding of the molecular processes underlying anthocyanin production in Chinese kale. Our comprehensive metabolomic and transcriptome analyses provide important insights into the regulatory system that controls anthocyanin production and transport, while providing a foundation for further research to elucidate the physiological importance of the metabolites found in this nutritionally significant vegetable.
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