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Updated: Jan 11, 2026

Spatiotemporal Control of Protein Activity through Optogenetic Allosteric Regulation
Published on: October 4, 2024
Illuminating the regulatory link between blue light and autophagy in photomorphogenesis
Lu Jiang1,2,3, Hong-Quan Yang1,2, Wenxiu Wang1,2
1Shanghai Key Laboratory of Plant Molecular Sciences, College of Life Sciences, Shanghai Normal University, Shanghai, China.
Abstract:
Cryptochrome 1 (CRY1) promotes photomorphogenesis primarily by inhibiting Constituttive photomorphogenic 1 (COP1)/Suppressor of PHYA-105 1 (SPA1)-mediated degradation of HY5 via the 26S proteasome degradation pathway. However, it remained unknown whether autophagy, a conserved vacuolar recycling process induced by nutrient starvation, also participates in blue light signaling. Our latest study reveals that in Arabidopsis thaliana, under nutrient starvation, Autophagy-related 8 (ATG8) binds and targets Elongated hypocotyl 5 (HY5) for vacuolar degradation in darkness, thereby promoting skotomorphogenesis. Upon blue-light activation, however, CRY1 binds to ATG8 and blocks its interaction with HY5, which in turn inhibits the autophagic degradation of HY5 and promotes photomorphogenesis. Our findings thus establish a direct photoreceptor - autophagy functional connection that integrates light and nutrient cues to govern developmental transitions in plants.
Insights
Blue light receptor CRY1 connects to autophagy to control plant development. CRY1 prevents HY5 degradation by autophagy in light, promoting photomorphogenesis, while blocking it in darkness to allow skotomorphogenesis.
Area of Science:
- Plant biology
- Molecular plant science
- Cellular signaling
Background:
- Cryptochrome 1 (CRY1) regulates photomorphogenesis by inhibiting COP1/SPA1-mediated HY5 degradation.
- The role of autophagy in blue light signaling pathways remained largely unexplored.
Purpose of the Study:
- To investigate the potential involvement of autophagy in blue light signaling in Arabidopsis thaliana.
- To elucidate the functional connection between photoreceptors and autophagy in integrating light and nutrient cues.
Main Methods:
- Yeast two-hybrid assays to detect protein-protein interactions.
- Co-immunoprecipitation assays to confirm interactions in vivo.
- Confocal microscopy to visualize protein localization and autophagy.
- Analysis of plant phenotypes under different light and nutrient conditions.
Main Results:
- Autophagy-related 8 (ATG8) targets Elongated hypocotyl 5 (HY5) for vacuolar degradation in darkness, promoting skotomorphogenesis.
- Blue light activates CRY1, which binds to ATG8 and inhibits HY5 autophagic degradation.
- CRY1-ATG8 interaction blocks ATG8-HY5 interaction, thereby promoting photomorphogenesis.
Conclusions:
- A direct functional link between a photoreceptor (CRY1) and autophagy is established.
- Autophagy acts as a crucial mediator integrating light and nutrient starvation signals.
- This integration governs plant developmental transitions between photomorphogenesis and skotomorphogenesis.
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