光调节蛋白激酶通过引导拟南芥 HY5 上的双功能磷酸代码微调植物光形态发生

IF 10.7 1区 生物学 Q1 CELL BIOLOGY
Nan Zhang, Chuang-Qi Wei, Da-Jin Xu, Zhi-Ping Deng, Ya-Chao Zhao, Lian-Feng Ai, Ying Sun, Zhi-Yong Wang, Sheng-Wei Zhang
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引用次数: 0

摘要

光形态发生是一种依赖光的植物生长发育程序。作为光形态发生的核心调控因子,ELONGATED HYPOCOTYL 5(HY5)受其转录活性和蛋白质稳定性动态变化的影响;然而,人们对这些过程的介质知之甚少。在这里,我们确定了拟南芥中与 HY5 相互作用并使其磷酸化的光合蛋白激酶 1(PPK1)就是这样一种媒介。PPK1 对 HY5 的磷酸化是与 B-BOX 蛋白 24(BBX24)和 CONSTITUTIVE PHOTOMORPHOGENIC 1(COP1)建立高亲和性结合的必要条件,这两种蛋白分别抑制 HY5 的转录活性并促进其降解。因此,PPKs 不仅在光照条件下调控 HY5 与其靶基因的结合,还在植物从光照转入黑暗时调控 HY5 的降解。我们的数据发现了一种 PPK 介导的 HY5 磷酸化密码,它整合了 HY5 的调控分子机制,从而精确控制植物的光形态发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Photoregulatory protein kinases fine-tune plant photomorphogenesis by directing a bifunctional phospho-code on HY5 in Arabidopsis

Photoregulatory protein kinases fine-tune plant photomorphogenesis by directing a bifunctional phospho-code on HY5 in Arabidopsis

Photomorphogenesis is a light-dependent plant growth and development program. As the core regulator of photomorphogenesis, ELONGATED HYPOCOTYL 5 (HY5) is affected by dynamic changes in its transcriptional activity and protein stability; however, little is known about the mediators of these processes. Here, we identified PHOTOREGULATORY PROTEIN KINASE 1 (PPK1), which interacts with and phosphorylates HY5 in Arabidopsis, as one such mediator. The phosphorylation of HY5 by PPK1 is essential to establish high-affinity binding with B-BOX PROTEIN 24 (BBX24) and CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), which inhibit the transcriptional activity and promote the degradation of HY5, respectively. As such, PPKs regulate not only the binding of HY5 to its target genes under light conditions but also HY5 degradation when plants are transferred from light to dark. Our data identify a PPK-mediated phospho-code on HY5 that integrates the molecular mechanisms underlying the regulation of HY5 to precisely control plant photomorphogenesis.

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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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