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MPK6‐mediated HY5 phosphorylation regulates light‐induced anthocyanin accumulation in apple fruit

花青素 磷酸化 生物 生物化学 蛋白激酶A 激酶 细胞生物学 bZIP域 转录因子 蛋白质磷酸化 基因 亮氨酸拉链 植物
作者
Yifan Xing,Wenjing Sun,Yuying Sun,Jialin Li,Jie Zhang,Ting Wu,Tingting Song,Yuncong Yao,Ji Tian
出处
期刊:Plant Biotechnology Journal [Wiley]
卷期号:21 (2): 283-301 被引量:36
标识
DOI:10.1111/pbi.13941
摘要

Summary Light is known to regulate anthocyanin pigment biosynthesis in plants on several levels, but the significance of protein phosphorylation in light‐induced anthocyanin accumulation needs further investigation. In this study, we investigated the dynamics of the apple fruit phosphoproteome in response to light, using high‐performance liquid chromatography–tandem mass spectrometry analysis. Among the differentially phosphorylated proteins, the bZIP (basic leucine zipper) transcription factor, HY5, which has been identified as an anthocyanin regulator, was rapidly activated by light treatment of the fruit. We hypothesized that phosphorylated MdHY5 may play a role in light‐induced anthocyanin accumulation of apple fruit. Protein interaction and phosphorylation assays showed that mitogen‐activated protein kinase MdMPK6 directly interacted with, and activated, MdHY5 via phosphorylation under light conditions, thereby increasing its stability. Consistent with this finding, the suppression of the mitogen‐activated protein kinase genes MdMPK6 or MdHY5 resulted in an inhibition of anthocyanin accumulation, and further showed that light‐induced anthocyanin accumulation is dependent on MdMPK6 kinase activity, and is required for maximum MdHY5 activity. Under light conditions, active MdMPK6 phosphorylated MdHY5 leading to accumulation of phospho‐MdHY5, which enhanced the binding of MdHY5 to its target anthocyanin related genes in fruit. Our findings reveal an MdMPK6–MdHY5 phosphorylation pathway in light‐induced anthocyanin accumulation, providing new insights into the regulation of light‐induced anthocyanin biosynthesis in apple fruit at both the transcriptional and post‐translational levels.
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