Abstract
Plants rely on water and light for photosynthesis, but water droplets on leaves can focus light into high-intensity spots, risking photodamage. Excessive light can impair growth or induce cell death, making it essential for plants to detect and respond to light fluctuations. While Ca2+ signaling has been linked to high light (HL) acclimation, the subcellular dynamics remain unclear. Here, we investigate Ca2+ responses to HL exposure in Arabidopsis thaliana. Using a glass bead to simulate light-focusing by water droplets, a biphasic increase of Ca2+ concentration was detected in the chloroplast stroma by the genetically encoded calcium indicator YC3.6 and confirmed using a newly established stroma-localized R-GECO1 (NTRC-R-GECO1). The stromal response was largely independent of light wavelength and unaffected in phot1 phot2 and cry1 cry2 mutants. Chemical inhibition of photosynthetic electron transport, microscopy-based Fv/Fm experiments, and measurement of the reactive oxygen species (ROS)-redox balance with roGFP-based reporters and Singlet Oxygen Sensor Green (SOSG) chemical dye suggested that photodamage and singlet oxygen contribute to the stromal Ca2+ response. While blue and white light also triggered a Ca2+ response in the cytosol and nucleus, pharmacological inhibition with cyclopiazonic acid (CPA) and loss-of-function mutants of the Ca2+ transporters BIVALENT CATION TRANSPORTER 2 (BICAT2) and endoplasmic reticulum (ER)-type Ca2+-ATPase (ECA) suggested that the HL response depends on a Ca2+ exchange between the ER and chloroplast stroma. The response was primarily light dependent but accelerated by increasing external temperature. This study implicates a novel Ca2+-mediated acclimation mechanism to HL stress, a process of growing relevance in the context of climate change.
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | P2642-2658.E7 |
| Fachzeitschrift | Current Biology |
| Jahrgang | 35 |
| Ausgabenummer | 11 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 9 Juni 2025 |
Fördermittel
This study was supported by the Knut and Alice Wallenberg Foundation (grant 2021.0071 to S.R. and S.S. and grant 2022.0029 to D.V. and M. Tenje), the European Research Council (Consolidator grant 101044878 to D.K., Q.Y., and S.S.), the Austrian Science Fund (Lise Meitner Program grant number M-2745-B to A.S.Z. and project P 37245-B to B.W. and M. Teige), the EU H2020-SFS-2019-2 RIA project ADAPT ( GA 2020 862-858 to B.W. and M. Teige), the Ministero dell'Istruzione, dell'Università e della Ricerca Fondo per Progetti di Ricerca di Rilevante Interesse Nazionale 2022 ( PRIN 2022NMSFHN ) (to A.C. and S.B.), and by the Agritech National Research Center and received funding from the European Union Next-GenerationEU (PIANO NAZIO-NALE DI RIPRESA E RESILIENZA [PNRR]—MISSIONE 4 COMPONENTE 2, INVESTIMENTO 1.4-D.D. 1032 17/06/2022, CN00000022 to B.M.O.M.). Part of the work was carried out with the support of the NOLIMITS Center of Excellence for Plant Biology and Other Life Sciences established by the University of Milan . M.S. thanks the Deutsche Forschungsgemeinschaft (DFG) for funding ( SCHW 1719/5-3 , SCHW 1719/10-1 , and SCHW 1719/11-1 ) and for the infrastructure grant INST 211/903-1 FUGG for the Zeiss LSM 980 confocal microscope as operated by the Imaging Network of the University of Münster ( RI_00497 ). K.Z. thanks the China Scholarship Council ( 202006910019 ) for a personal PhD studentship. We thank Vincent Allouch for assistance with the design of the hypothetical model, various people for providing mutant Arabidopsis seeds as detailed in the material and methods, Melanie Krebs (Heidelberg University, Germany) for the pGPTVII-Bar-U-RGECO1 plasmid, and Jens Staal (VIB, Belgium) for the pICOz plasmid.
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
-
SDG 13 – Maßnahmen zum Klimaschutz
ÖFOS 2012
- 106022 Mikrobiologie
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