FaTRAB1是一种bZIP转录因子,通过组织特异性调控促进草莓叶片花青素的生物合成。

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2025-09-24 eCollection Date: 2025-09-01 DOI:10.1371/journal.pgen.1011888
Min Yang, Chenghui Song, Yuanxiu Lin, Yunting Zhang, Mengyao Li, Qing Chen, Yong Zhang, Haoru Tang, Ya Luo
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引用次数: 0

摘要

bZIP转录因子FaTRAB1作为植物适应环境胁迫的中心调控因子已被广泛研究。然而,其在调节花青素生物合成中的作用尚不清楚。本研究揭示了FaTRAB1在草莓叶片(Fragaria vesca 'Ruegen‘)和果实(Fragaria × ananassa ’Benihoppe')中调节花青素积累的新功能。FaTRAB1是一种核质定位蛋白,在叶片和绿色小果实中表达量相对较高。在‘Ruegen’草莓中稳定过表达FaTRAB1显著提高了幼叶、成熟叶和老叶的花青素水平。质谱和高效液相色谱分析鉴定出成熟草莓叶片中主要的三种花青素:花青素-3- o -葡萄糖苷(C3G)和花青素-3,5- o -二葡糖苷(C3,5dG)(78.91%),芍药苷-3,5- o -二葡糖苷(Pg3,5dG, 12.6%),芍药苷-3- o -葡萄糖苷(Pg3G, 8.49%)为次要成分。蛋白相互作用分析表明,FaTRAB1可能与FabHLH3竞争,与FaMYB10和FaTTG1结合,形成一个新的调控复合体,协调激活花青素结构基因(FaF3'H, FaANS, FaUFGT和FaOMT)的启动子。该机制优先促进花青素衍生物(C3,5dG和C3G)在叶片中的积累,导致红紫色色素沉着,而Pg3,5dG和痕量Pg3G起次要作用。相比之下,草莓果实主要积累Pg3G。有趣的是,FaTRAB1可能会轻微抑制FaMYB10/ fattg1介导的水果中Pg3G和花青素基花青素的生物合成。相反,它主要通过与FaF3'H的协同作用来促进C3G的积累,导致叶片和果实之间不同的色素沉着模式。这些发现阐明了FaTRAB1在草莓花青素积累中的组织特异性调节作用,为器官特异性着色机制提供了重要见解。本研究为通过有针对性的遗传操作提高草莓颜色品质奠定了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FaTRAB1, a bZIP transcription factor, enhances anthocyanin biosynthesis in strawberry leaves via tissue-specific regulation.

The bZIP transcription factor FaTRAB1 has been extensively studied as a central regulator of plant adaptation to environmental stresses. However, its role in modulating anthocyanin biosynthesis remains unclear. This study reveals a novel function of FaTRAB1 in regulating anthocyanin accumulation in both strawberry leaves (Fragaria vesca 'Ruegen') and fruits (Fragaria × ananassa 'Benihoppe'). FaTRAB1 is a nucleocytoplasmic-localized protein, exhibiting relatively higher expression in leaves and small green fruits. Stable overexpression of FaTRAB1 in 'Ruegen' strawberry significantly enhanced anthocyanin levels in young, mature, and old leaves. Mass spectrometry and HPLC analysis identified three major anthocyanins in mature strawberry leaves: cyanidin-3-O-glucoside (C3G) and cyanidin-3,5-O-diglucoside (C3,5dG) (78.91%), and peonidin-3,5-O-diglucoside (Pg3,5dG, 12.6%), with pelargonidin-3-O-glucoside (Pg3G, 8.49%) as a minor component. Protein interaction assays demonstrated that FaTRAB1 likely competes with FabHLH3 for binding to FaMYB10 and FaTTG1, forming a novel regulatory complex that coordinately activates the promoter of anthocyanin structural genes (FaF3'H, FaANS, FaUFGT, and FaOMT). This mechanism preferentially promotes the accumulation of cyanidin derivatives (C3,5dG and C3G) in leaves, resulting in reddish-purple pigmentation, while Pg3,5dG and trace Pg3G contribute secondarily. In contrast, strawberry fruits predominantly accumulate Pg3G. Intriguingly, FaTRAB1 may slightly suppress FaMYB10/FaTTG1-mediated biosynthesis of Pg3G and cyanidin-based anthocyanins in fruits. Instead, it primarily enhances C3G accumulation through synergistic interaction with FaF3'H, leading to distinct pigmentation patterns between leaves and fruits. These findings elucidate the tissue-specific regulatory role of FaTRAB1 in strawberry anthocyanin accumulation, providing critical insights into organ-specific coloration mechanisms. This work establishes a theoretical foundation for improving strawberry color quality through targeted genetic manipulation.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
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438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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