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PpMYB15 和 PpMYBF1 转录因子参与调控桃果实类黄酮生物合成。

PpMYB15 and PpMYBF1 Transcription Factors Are Involved in Regulating Flavonol Biosynthesis in Peach Fruit.

机构信息

Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology , Zhejiang University , Hangzhou 310058 , China.

出版信息

J Agric Food Chem. 2019 Jan 16;67(2):644-652. doi: 10.1021/acs.jafc.8b04810. Epub 2019 Jan 8.

DOI:10.1021/acs.jafc.8b04810
PMID:30525549
Abstract

Flavonoids are major polyphenol compounds in plants and contribute substantially to the health-promoting benefits of fruit and vegetables. Peach is rich in polyphenols with flavonols as the main flavonoids. To investigate the regulation of flavonol biosynthesis in peach fruit, two R2R3-MYB transcription factor (TF) genes, PpMYB15 and PpMYBF1, were isolated and characterized. Sequence analysis revealed that the PpMYB15 and PpMYBF1 proteins are members of the flavonol clade of the R2R3-MYB family. Real-time quantitative PCR analysis showed that PpMYB15 and PpMYBF1 transcript levels correlated well with the flavonol content and the expression of flavonol synthase ( PpFLS1) in different fruit samples. Dual-luciferase assays indicated that both PpMYB15 and PpMYBF1 could trans-activate promoters of flavonoid biosynthesis genes, including chalcone synthase ( PpCHS1), chalcone isomerase ( PpCHI1), flavanone 3-hydroxylase ( PpF3H), and PpFLS1. Transient overexpression of 35S::PpMYB15 or 35S::PpMYBF1 both triggered flavonol biosynthesis but not anthocyanin and proanthocyanidin biosynthesis in tobacco leaves. In transgenic tobacco flowers, overexpression of 35S::PpMYB15 or 35S::PpMYBF1 caused a significant increase in flavonol levels and significantly reduced anthocyanin accumulation, resulting in pale-pink or pure white flowers. These results suggest that PpMYB15 and PpMYBF1 are functional flavonol-specific positive regulators in peach fruit and are important candidates for biotechnological engineering flavonol biosynthesis in plants.

摘要

类黄酮是植物中主要的多酚化合物,对水果和蔬菜的促进健康益处有重要贡献。桃富含多酚,其中以类黄酮为主要类黄酮。为了研究桃果实中类黄酮生物合成的调控,分离并鉴定了两个 R2R3-MYB 转录因子(TF)基因 PpMYB15 和 PpMYBF1。序列分析表明,PpMYB15 和 PpMYBF1 蛋白是 R2R3-MYB 家族类黄酮分支的成员。实时定量 PCR 分析表明,PpMYB15 和 PpMYBF1 的转录水平与不同果实样品中的类黄酮含量和类黄酮合酶(PpFLS1)的表达密切相关。双荧光素酶报告基因分析表明,PpMYB15 和 PpMYBF1 均可激活类黄酮生物合成基因的启动子,包括查尔酮合酶(PpCHS1)、查尔酮异构酶(PpCHI1)、黄烷酮 3-羟化酶(PpF3H)和 PpFLS1。瞬时过表达 35S::PpMYB15 或 35S::PpMYBF1 均可在烟草叶片中触发类黄酮生物合成,但不能触发花青素和原花青素生物合成。在转基因烟草花朵中,过表达 35S::PpMYB15 或 35S::PpMYBF1 导致类黄酮水平显著增加,花青素积累显著减少,导致花朵呈淡粉色或纯白色。这些结果表明 PpMYB15 和 PpMYBF1 是桃果实中功能性类黄酮特异性正调控因子,是植物中类黄酮生物合成生物技术工程的重要候选基因。

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