Xue Qiqin, Zhang Xiurong, Yang Hui, Li Huadong, Lv Yuying, Zhang Kun, Liu Yongguang, Liu Fengzhen, Wan Yongshan
State Key Laboratory of Crop Biology, Shandong Key Laboratory of Crop Biology, College of Agronomy, Shandong Agricultural University, Tai'an, 271018 Shandong, China.
Weifang University of Science and Technology, Shouguang, 262700 Shandong, China.
Int J Genomics. 2021 Aug 6;2021:5883901. doi: 10.1155/2021/5883901. eCollection 2021.
Peanut ( L.) is an important source of oil and food around the world, and the testa color affects its appearance and commercial value. However, few studies focused on the mechanism of pigment formation in peanut testa. In this study, cultivars Shanhua 15 with pink testa and Zhonghua 12 with red testa were used as materials to perform the combined analysis of transcriptome and metabolome. A total of 198 flavonoid metabolites were detected, among which petunidin 3-O-glucoside and cyanidin O-acetylhexoside in Zhonghua12 were 15.23 and 14.72 times higher than those of Shanhua 15 at the R7 stage, revealing the anthocyanins underlying the red testa. Transcriptome analysis showed that there were 6059 and 3153 differentially expressed genes between Shanhua 15 and Zhonghua 12 in different growth periods, respectively. These differentially expressed genes were significantly enriched in the flavonoid biosynthesis, biosynthesis of secondary metabolites, and metabolic pathways. Integrated analysis of transcriptome and metabolome indicated CHS gene (), F3'H genes ( and ), and DFR genes ( and ) may be the key functional genes controlling the formation of pink and red testa in peanut. Transcription factors MYB (, , , , and ), bHLH (N, , and ), and WD40 () in the biosynthetic pathway of anthocyanin were significantly upregulated in Zhonghua 12 which may be the key regulatory genes in testa pigment formation. This is a comprehensive analysis on flavonoid metabolites and related genes expression in peanut testa, providing reference for revealing the regulatory mechanism of pigment accumulation in peanut testa.
花生(Arachis hypogaea L.)是全球重要的油料和粮食来源,种皮颜色影响其外观和商业价值。然而,关于花生种皮色素形成机制的研究较少。本研究以种皮为粉色的山花15和种皮为红色的中花12为材料,进行转录组和代谢组联合分析。共检测到198种黄酮类代谢产物,其中中花12在R7期的矮牵牛素3 - O - 葡萄糖苷和花青素O - 乙酰己糖苷分别比山花15高15.23倍和14.72倍,揭示了红色种皮的花青素成分。转录组分析表明,山花15和中花12在不同生长时期分别有6059个和3153个差异表达基因。这些差异表达基因在黄酮类生物合成、次生代谢物生物合成和代谢途径中显著富集。转录组和代谢组的综合分析表明,CHS基因()、F3'H基因(和)以及DFR基因(和)可能是控制花生粉色和红色种皮形成的关键功能基因。花青素生物合成途径中的转录因子MYB(、、、、和)、bHLH(N、和)以及WD40()在中花12中显著上调,可能是种皮色素形成的关键调控基因。这是对花生种皮黄酮类代谢产物及相关基因表达的综合分析,为揭示花生种皮色素积累的调控机制提供参考。