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

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, <i>PIF4</i> is epistatic to <i>NPR1</i> 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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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2024-12-19
DOI
https://doi.org/10.1073/pnas.2412755121
Citations
14
Primary Topic
Light effects on plants
Type
article
Field-Weighted Citation Impact
8.39

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article

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

Xing Wang Deng, Yunyun Zhuang, Yaqi Tang, Yangyang Zhou et al.
14 citations
Proceedings of the National Academy of Sciences
Light effects on plants
8.39
article

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

Xing Wang Deng, Yunyun Zhuang, Yaqi Tang, Yangyang Zhou, Jigang Li, Pengtao Liu, Kai Xu, Xiaoting Li, Li Yang, Yaru Tang, Guangming He, Jie Liu, Zhi Zhou
article en
14 citations

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, <i>PIF4</i> is epistatic to <i>NPR1</i> 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.

Proceedings of the National Academy of SciencesVol. 121(52)
Peking University (CN), King Center (US), Center for Life Sciences (CN), China Agricultural University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, Chinese Universities Scientific Fund
Life in Land
Openalex Percentile: Top 2%
Light effects on plants
8.39
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