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‘锦绣’桃果皮中天然缺色和紫外诱导花色苷积累的分子机制。

Molecular mechanisms underlying natural deficient and ultraviolet-induced accumulation of anthocyanin in the peel of 'Jinxiu' peach.

机构信息

College of Agriculture & Biotechnology, Zijingang Campus, Zhejiang University, Hangzhou, China.

New Zealand Institute for Plant & Food Research Limited, Auckland, New Zealand.

出版信息

Plant Cell Environ. 2024 Dec;47(12):4833-4848. doi: 10.1111/pce.15064. Epub 2024 Aug 5.

DOI:10.1111/pce.15064
PMID:39101482
Abstract

Peach varieties that differ in red coloration due to varied anthocyanin accumulation result from transcriptional regulation by PpMYB10s, a group of specific R2R3 MYBs. Here we investigated the mechanisms driving a lack of anthocyanin in yellow-skinned 'Jinxiu' peach peel, as well as accumulation induced by UV irradiance. It was found that PpMYB10.1, PpMYB10.2 and PpMYB10.3 were positive regulators of anthocyanin accumulation, but the stimulation by PpMYB10.2 was weak. Low expression of PpMYB10.1 causes natural anthocyanin deficiency in 'Jinxiu' peel. However, the promoter sequences of PpMYB10.1 were identical in 'Jinxiu' and a naturally red-coloured peach 'Hujingmilu'. Therefore, potential negative regulator(s) upstream of PpMYB10.1 were explored. A novel R2R3-MYB repressor termed PpMYB80 was identified through comparative transcriptomic analysis and then functionally confirmed via transiently overexpressing and silencing in peach fruit, as well as transformation in tobacco. PpMYB80 directly binds to the promoter of PpMYB10.1 and inhibits its expression, but does not affect PpMYB10.3. In UV-exposed 'Jinxiu' fruit, expression of PpMYB10.3 was upregulated, while PpMYB10.1 remained low and PpMYB80 enhanced, which results in accumulation of anthocyanin in peel. This study revealed a transcriptional cascade involving PpMYB activators and repressors in regulating basal and UV-induced anthocyanin accumulation in peach peel.

摘要

因花色苷积累程度不同而呈现不同红色的桃品种,是由 PpMYB10s(一组特定的 R2R3 MYB)转录调控的结果。本研究调查了导致黄色果皮‘锦绣’桃缺乏花色苷以及紫外线照射诱导花色苷积累的机制。结果发现,PpMYB10.1、PpMYB10.2 和 PpMYB10.3 是花色苷积累的正调控因子,但 PpMYB10.2 的刺激作用较弱。PpMYB10.1 的低表达导致‘锦绣’果皮中天然花色苷缺乏。然而,‘锦绣’和一种天然红色桃‘沪晶蜜露’的 PpMYB10.1 启动子序列相同。因此,研究人员探索了 PpMYB10.1 上游的潜在负调控因子。通过比较转录组分析,发现了一种新的 R2R3-MYB 抑制剂 PpMYB80,然后通过在桃果实中瞬时过表达和沉默以及在烟草中转化进行了功能验证。PpMYB80 直接结合 PpMYB10.1 的启动子并抑制其表达,但不影响 PpMYB10.3。在紫外线照射的‘锦绣’果实中,PpMYB10.3 的表达上调,而 PpMYB10.1 仍然较低,PpMYB80 增强,导致果皮中花色苷的积累。本研究揭示了一个涉及 PpMYB 激活子和抑制剂的转录级联反应,该反应参与调控桃果皮中基础和紫外线诱导的花色苷积累。

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