bioRxiv Science⌕ Search

bioRxiv · 10.1101/2023.12.22.573105

Phosphorylated transcription factor PuHB40 is involved in ROS-dependent anthocyanin biosynthesis in pear exposed to high-light stress

Abstract

As sessile organisms, plants are increasingly vulnerable to environmental stresses because of global warming and climate change. Stress-induced reactive oxygen species (ROS) accumulation results in plant cell damages and even cell death. Anthocyanins are important antioxidants that scavenge ROS to maintain ROS homeostasis. However, the mechanism underlying ROS-induced anthocyanin accumulation is unclear. In this study, we determined that in pear the HD-Zip I family member PuHB40 mediates ROS-dependent anthocyanin biosynthesis under high-light stress. Specifically, PuHB40 is a transcription factor that induces PuMYB123-like/PubHLH3 complex for anthocyanin biosynthesis. The transcriptional activation by PuHB40 depends on its phosphorylation level, which is regulated by protein phosphatase 2A (PP2A). High ROS contents maintain the phosphorylation of PuHB40 at a high level, while also enhancing PuHB40-induced PuMYB123-like transcription by decreasing the transcription of PuPP2AA2, ultimately leading to increased anthocyanin biosynthesis. Our study revealed the pathway regulating ROS-induced anthocyanin biosynthesis in pear, further clarifying the mechanism underlying abiotic stress-induced anthocyanin biosynthesis, which may have implications for improving plant stress tolerance. IN A NUTSHELLO_ST_ABSBackgroundC_ST_ABSVarious abiotic stresses, including high-light intensity, promote the accumulation of anthocyanins in plants, while also activating the production of reactive oxygen species (ROS). Anthocyanins can attenuate the negative effects of high-light stress by acting as antioxidants that restrict ROS accumulation. Several reports have shown that ROS can stimulate anthocyanin accumulation, but whether high-light stress-induced anthocyanin accumulation depends on ROS is undetermined. Additionally, the mechanism underlying ROS-dependent anthocyanin biosynthesis remains unclear. QuestionDoes high-light stress-induced anthocyanin biosynthesis depend on ROS? What is the molecular basis of high-light stress-induced anthocyanin biosynthesis? FindingsHigh-light stress-induced anthocyanin biosynthesis in pear seedlings is dependent on ROS accumulation. PuMYB123-like is the key MYB transcription factor for anthocyanin biosynthesis, while PuHB40 activates anthocyanin biosynthesis in response to ROS under high-light stress. Specifically, PuHB40 activates the transcription of PuMYB123-like, with the encoded protein combining with PubHLH3 to form an MBW complex that promotes anthocyanin biosynthesis. The transcriptional activation by PuHB40 depends on its phosphorylation status, which is regulated by protein phosphatase 2A (PP2A). High ROS levels inhibit the transcription of PuPP2AA2, thereby maintaining the phosphorylation of PuHB40, enhancing the transcriptional activation by PuHB40, inducing PuMYB123-like transcription, and ultimately leading to increased anthocyanin biosynthesis. Next stepsOur future research will focus on whether ROS and the MYB123-like- PuHB40-PP2A regulatory module are also involved in the anthocyanin biosynthesis induced by other abiotic and biotic stresses, which will provide insights into biotic stress-induced anthocyanin biosynthesis and form the theoretical basis for improving fruit coloration.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bai, S., Zhang, L., Wang, L., Gao, Y., Yang, S., Su, J., Ni, J., Teng, Y.. 2023-12-23. Phosphorylated transcription factor PuHB40 is involved in ROS-dependent anthocyanin biosynthesis in pear exposed to high-light stress. https://doi.org/10.1101/2023.12.22.573105

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

In-cell structural analysis reveals a distinctive chloroplast ribosome in Chlamydomonas reinhardtii

Chloroplast ribosomes synthesize plastid-encoded components of photosynthetic machinery, yet their structure and organization remain poorly understood. We combined cryo-focused ion beam milling, cryo-electron tomography and subtomogram averaging to determine native chloroplast ribosomes in Chlamydomonas reinhardtii. The 4.4-4.9 [A] structure revealed a large arch-like extension on the small subunit (SSU). Comparisons with bacterial and plant chloroplast ribosomes, supported by proteomics, AlphaFold3 predictions and a recent atomic model, indicate that the arch is formed by insertions and extensions in SSU proteins. Classification resolved active, thylakoid-associated ribosomes with density adjacent to the nascent peptide exit and an arch-moved state enriched among thylakoid-associated particles, with coordinated displacement of the arch and beak. Phylogenetic analysis revealed an evolutionary mosaic: the uS3c insertion is broadly distributed across Chlorophyceae, whereas the uS2c insertion, uS5c and PSRP7 are concentrated in Chlamydomonadales, with PSRP7 also in Sphaeropleales. Nuclear-encoded components were recruited stepwise onto a plastid-encoded scaffold, with all four under comparable purifying selection. These findings link a lineage-specific SSU extension to ribosome dynamics, thylakoid association and evolution, highlighting the value of in-cell structural analysis.

plant biology↗

Implementation and calibration of the Vaganov-Shashkin model in the virtualRings R package

Process-based tree growth models provide a mechanistic framework for investigating how climate conditions regulate tree growth across daily to annual time scales. Yet, their broader application across species and environments is constrained by the limited accessibility in open-source environments and the difficulty of estimating physiological parameters that are rarely measured directly. Here, we present virtualRings, a new R package integrating the Vaganov-Shashkin model (VSM) and the RINGS3 models, and focus on the implementation and calibration of VSM. Using tree-ring width observations from seven Northern Hemisphere sites across various environmental conditions, we compared the traditional bootstrap-based calibration approach with the Covariance Matrix Adaptation Evolution Strategy (CMA-ES). CMA-ES improved agreement between simulated and observed radial tree growth and provided an efficient approach for model parameter estimation. We further evaluated practical CMA-ES settings to balance computational cost and performance and discussed its potential limitations. The virtualRings package provides an open and reproducible platform for tree growth simulation, facilitating the application of important process-based models across species and environments and the investigation of how temperature and moisture constraints regulate daily tree-ring formation across spatial and temporal scales.

plant biology↗

Timing of transient darkness shapes carbon-nitrogen metabolism and sugar signaling in sugarcane

Fluctuating light is common in field environments. Yet, the mechanisms by which C4 crops coordinate carbon and nitrogen metabolism during short-term carbon deprivation remain poorly understood. Here, we imposed transient darkness at different phases of the diel cycle to assess how the timing of light loss affects photosynthesis, carbohydrate turnover, amino acid dynamics, and sugar-sensing pathways in commercial sugarcane leaves. Early-day darkness significantly impaired photosynthetic induction and revealed a temporal disconnect between stomatal and metabolic limitations, whereas midday and late-day treatments caused temporary, time-specific disruptions in carbon assimilation. These shifts altered the balance between sucrose preservation and catabolic mobilization, leading to treatment-dependent changes in starch reserves and free amino acids. Core circadian components largely maintained their phase relationships, but their amplitudes varied across treatments, consistent with partial decoupling from carbon status. Darkness also reorganized energy signaling, with SnRK1 and DIN6 responses associated with greater declines in sucrose. Notably, trehalose-pathway transcripts showed marked changes in network connectivity, with ScTPSIIG consistently emerging as a highly connected candidate associated with photosynthetic performance, water-use traits, sugar sensing, and amino acid metabolism. Overall, these results indicate that the timing of carbon limitation and residual sucrose availability shape distinct metabolic responses, while trehalose metabolism provides a candidate regulatory layer coordinating carbon-nitrogen adjustment during the diel cycle, highlighting class II TPS proteins as targets for functional investigation of metabolic resilience in sugarcane.

plant biology↗