NPR1 promotes blue light–induced plant photomorphogenesis by ubiquitinating and degrading PIF4

IF 9.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2024-12-19 DOI:10.1073/pnas.2412755121
Yangyang Zhou, Pengtao Liu, Yaqi Tang, Jie Liu, Yaru Tang, Yumeng Zhuang, Xiaoting Li, Kaiqi Xu, Zhi Zhou, Jigang Li, Guangming He, Xing Wang Deng, Li Yang
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Abstract

Light is a major determinant of plant growth and survival. NONEXPRESSER OF PATHOGENESIS-RELATED GENES 1 (NPR1) acts as a receptor for salicylic acid (SA) and serves as the key regulator of SA-mediated immune responses. However, the mechanisms by which plants integrate light and SA signals in response to environmental changes, as well as the role of NPR1 in regulating plant photomorphogenesis, remain poorly understood. This study shows that SA promotes plant photomorphogenesis by regulating PHYTOCHROME INTERACTING FACTOR 4 (PIF4). Specifically, NPR1 promotes photomorphogenesis under blue light by facilitating the degradation of PIF4 through light-induced polyubiquitination. NPR1 acts as a substrate adaptor for the CULLIN3-based E3 ligase, which ubiquitinates PIF4 at Lys129, Lys252, and Lys428, and leading to PIF4 degradation via the 26S proteasome pathway. Genetically, PIF4 is epistatic to NPR1 in the regulation of blue light–induced photomorphogenesis, suggesting it acts downstream of NPR1. Furthermore, cryptochromes mediate the polyubiquitination of PIF4 by NPR1 in response to blue light by promoting the interaction and ubiquitination between NPR1 and PIF4. Transcriptome analysis revealed that under blue light, NPR1 and PIF4 coordinately regulate numerous downstream genes related to light and auxin signaling pathways. Overall, these findings unveil a role for NPR1 in photomorphogenesis, highlighting a mechanism for posttranslational regulation of PIF4 in response to blue light. This mechanism plays a pivotal role in the fine-tuning of plant development, enabling plants to adapt to complex environmental changes.
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光是植物生长和存活的主要决定因素。NONEXPRESSER OF PATHOGENESIS-RELATED GENES 1(NPR1)是水杨酸(SA)的受体,也是 SA 介导的免疫反应的关键调节因子。然而,人们对植物整合光和 SA 信号以应对环境变化的机制以及 NPR1 在调控植物光形态发生中的作用仍然知之甚少。本研究表明,SA通过调控PHYTOCHROME INTERACTING FACTOR 4(PIF4)促进植物的光形态发生。具体来说,NPR1通过光诱导的多泛素化促进PIF4的降解,从而在蓝光下促进光形态发生。NPR1 是基于 CULLIN3 的 E3 连接酶的底物适配体,它在 Lys129、Lys252 和 Lys428 处泛素化 PIF4,导致 PIF4 通过 26S 蛋白酶体途径降解。从遗传学角度看,PIF4 在调控蓝光诱导的光形态发生方面与 NPR1 具有外显性,这表明它作用于 NPR1 的下游。此外,隐色体通过促进 NPR1 和 PIF4 之间的相互作用和泛素化,介导 NPR1 在响应蓝光时对 PIF4 的多泛素化。转录组分析表明,在蓝光下,NPR1 和 PIF4 协调调控与光和叶绿素信号通路相关的许多下游基因。总之,这些发现揭示了 NPR1 在光形态发生中的作用,强调了 PIF4 在响应蓝光时的翻译后调控机制。这一机制在植物发育的微调中发挥着关键作用,使植物能够适应复杂的环境变化。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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