Wang Jiao, Sun Lei, Jiao Bo, Zhao Pu, Xu Tianyun, Gu Sa, Huo Chenmin, Pang Jianzhou, Zhou Shuo
Institute of Biotechnology and Food Science, Hebei Academy of Agriculture and Forestry Sciences/Hebei Key Laboratory of Plant Genetic Engineering, Shijiazhuang, 050000, China.
Hebei University of Economics and Business, Shijiazhuang, 050000, China.
BMC Genom Data. 2025 Jan 13;26(1):3. doi: 10.1186/s12863-024-01294-y.
Wheat seeds display different colors due to the types and contents of anthocyanins, which is closely related to anthocyanin metabolism. In this study, a transcriptomic and metabolomic analysis between white and purple color wheat pericarp aimed to explore some key genes and metabolites involved in anthocyanin metabolism.
Two wheat cultivars, a white seed cultivar Shiluan02-1 and purple seed cultivar Hengzi151 were used to identify the variations in differentially expressed genes (DEGs) and differentially accumulated flavonoids (DAFs). Based on metabolomic data, 314 metabolites and 191 DAFs were identified. Chalcone, flavonol, pro-anthocyanidin and anthocyanidin were the most differentially accumulated flavonoid compounds in Hengzi151. 2610 up-regulated and 2668 down-regulated DEGs were identified according to transcriptomic data. The results showed that some structural genes in anthocyanin synthesis pathway were prominently activated in Hengzi151, such as PAL, CAD, CHS and so on. Transcription factors (TFs) of MYB, bHLH, WD40 and some other TFs probably involved in regulating anthocyanin biosynthesis were identified. Some genes from hormone synthetic and signaling pathways that may participate in regulating anthocyanin biosynthesis also have been identified.
Our results provide valuable information on the candidate genes and metabolites involved in the anthocyanin metabolism in wheat pericarp.
由于花青素的类型和含量不同,小麦种子呈现出不同颜色,这与花青素代谢密切相关。本研究对白色和紫色小麦果皮进行转录组和代谢组分析,旨在探索参与花青素代谢的一些关键基因和代谢产物。
使用两个小麦品种,白粒品种石栾02-1和紫粒品种衡紫151来鉴定差异表达基因(DEGs)和差异积累黄酮类化合物(DAFs)的变化。基于代谢组数据,鉴定出314种代谢产物和191种DAFs。查尔酮、黄酮醇、原花青素和花青素是衡紫151中差异积累最显著的黄酮类化合物。根据转录组数据,鉴定出2610个上调和2668个下调的DEGs。结果表明,花青素合成途径中的一些结构基因在衡紫151中被显著激活,如PAL、CAD、CHS等。鉴定出可能参与调控花青素生物合成的MYB、bHLH、WD40等转录因子(TFs)。还鉴定出一些可能参与调控花青素生物合成的激素合成和信号通路中的基因。
我们的结果为小麦果皮中参与花青素代谢的候选基因和代谢产物提供了有价值的信息。