Metabolome and transcriptome landscapes reveal potential genes and metabolites involved in formation of leaf color in red-leafed apple mutants

生物 转录组 类黄酮生物合成 天竺葵苷 小桶 代谢途径 代谢组 突变体 花青素 生物化学 代谢组学 基因 下调和上调 生物合成 花青素 氰化物 遗传学 代谢物 RNA序列 染色质免疫沉淀 从头转录组组装 基因表达谱 颜料 次生代谢 苯丙素 查尔酮异构酶 MYB公司 结构基因 植物生理学 苹果属植物 类黄酮 植物 基因表达调控
作者
Tingting Sun,Junke Zhang,Xingliang Li,Minji Li,Qiang Zhang,Yuzhang Yang,Jia Zhou,Wei QinPing,Beibei Zhou
出处
期刊: [Springer Science+Business Media]
卷期号:4 (1)
标识
DOI:10.1007/s44281-026-00111-z
摘要

Abstract Leaf color mutations in plants serve as valuable resources for investigating metabolic pathways related to biosynthesis of chlorophyll, flavonoid, and carotenoid. In this study, a comprehensive analysis of the physiological characteristics, transcriptomes, and metabolomic profiles of a mutant of Malus hupehensis var. pingyiensis with red leaves (RM) and normal plant (CK) with green leaves was performed. A total of 283 differentially abundant metabolites (DAMs) and 9,822 differentially expressed genes (DEGs) were identified between RM and CK. Compared with the CK, RM presented a reduced chlorophyll content and elevated levels of carotenoids, flavonoids, and anthocyanins. KEGG pathway enrichment analysis revealed that the DAMs and DEGs were associated mainly with the metabolism of chlorophyll, carotenoids, and flavonoids, with the anthocyanidin biosynthesis pathway showing the greatest enrichment. Several key anthocyanin biosynthetic genes, including chalcone isomerase ( CHI ), dihydroflavonol 4-reductase ( DFR ), UDP-Glucose:Flavonoid 3-O-Glucosyltransferase ( UFGT ), and UDP-glycosyltransferases ( UGT ), were upregulated in the red leaves, in line with a significant increase in cyanidin 3-O-glucoside (C3G) and pelargonidin 3-O-glucoside (pg3G). Furthermore, RNA sequencing (RNA-seq) analysis revealed upregulation of MdMYB10 and MdUFGT . Yeast one-hybrid (Y1H), chromatin immunoprecipitation (ChIP), and dual-luciferase reporter (LUC) assays demonstrated that MdMYB10 bound to the MdUFGT promoter fragment and subsequently upregulated its expression, leading to the accumulation of C3G and pg3G in RM. Our findings provide new insights into the regulatory mechanisms of leaf coloration and offer a foundation for the development of new cultivars with alteration of leaf color.
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