Integrative transcriptomic and metabolomic analyses reveal the flavonoid biosynthesis of Pyrus hopeiensis flowers under cold stress

类黄酮生物合成 转录组 类黄酮 小桶 生物 MYB公司 代谢组学 代谢组 基因 结构基因 生物合成 WRKY蛋白质结构域 生物化学 代谢途径 遗传学 基因表达 植物 生物信息学 突变体 抗氧化剂
作者
Yongtan Li,Jun Zhang,Shijie Wang,Haie Zhang,Yichao Liu,Minsheng Yang
出处
期刊:Horticultural Plant Journal [Elsevier]
卷期号:9 (3): 395-413 被引量:14
标识
DOI:10.1016/j.hpj.2022.11.004
摘要

Low temperature is among the most restrictive factors to limit the yield and distribution of pear. Pyrus hopeiensis is a valuable wild resource. PCA showed that P. hopeiensis had strong cold resistance. In this study, the mRNA and metabolome sequencing of P. hopeiensis flower organs exposed to different low temperatures were performed to identify changes of genes and metabolites in response to low-temperature stress. A total of 4 851 differentially expressed genes (DEGs) were identified. Trend analysis showed that these DEGs were significantly enriched in profiles 19, 18, 7, 14, 1, 4 and 11. And the KEGG enrichment analysis showed that the DEGs in profile 18 were significantly enriched in flavone and flavonol biosynthesis. Besides, the expressed trends as well as GO and KEGG functional enrichment analyses of DEGs under cold and freezing stress showed significantly difference. Analyses of flavonoid-related pathways indicated that flavonoid structural genes had undergone significant changes. Correlation analysis showed that bHLH and MYB TFs may affect flavonoid biosynthesis by regulating structural gene expression. And PhMYB308 and PhMYB330 were likely candidate repressors of flavonoid biosynthesis by binding to a specific site in bHLH proteins. In total, 92 differentially accumulated metabolites (DAMs) were identified in P. hopeiensis flowers including 12 flavonoids. WGCNA results showed that coral1, pink and brown4 modules were closely associated with flavonoids and 11 MYBs and 15 bHLHs among the three modules may activate or inhibit the expression of 23 structural genes of flavonoid biosynthesis. Taken together, the results of this study provided a theoretical basis for further exploration of the molecular mechanisms of flavonoid biosynthesis and cold resistance of P. hopeiensis flower organs and our findings laid a foundation for further molecular breeding in cold-resistant pear varieties.
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