Light on its feet: Acclimation to high and low diurnal light is flexible in Chlamydomonas reinhardtii
Authors: Dupuis, S., Chastain, J. L., Han, G., Zhong, V., Gallaher, S. D., Nicora, C. D., Purvine, S. O., Lipton, M. S., Niyogi, K. K., Iwai, M., Merchant, S. S.
The study examined how prior light‑acclimation influences the fitness and rapid photoprotective reprogramming of Chlamydomonas during transitions between low and high diurnal light intensities. While high‑light‑acclimated cells struggled to grow and complete the cell cycle after shifting to low light, low‑light‑acclimated cells quickly remodeled thylakoid ultrastructure, enhanced photoprotective quenching, and altered photosystem protein levels, recovering chloroplast function within a single day. Transcriptomic and proteomic profiling revealed swift induction of stress‑response genes, indicating high flexibility in diurnal light acclimation.
The study introduces a native‑condition method combining cell fractionation and immuno‑isolation to purify autophagic compartments from Arabidopsis, followed by proteomic and lipidomic characterisation of the isolated phagophore membranes. Proteomic profiling identified candidate proteins linked to autophagy, membrane remodeling, vesicular trafficking and lipid metabolism, while lipidomics revealed a predominance of glycerophospholipids, especially phosphatidylcholine and phosphatidylglycerol, defining the unique composition of plant phagophores.
The study employed computational approaches to characterize the SUMOylation (ULP) machinery in Asian rice (Oryza sativa), analyzing phylogenetic relationships, transcriptional patterns, and protein structures across the reference genome, a population panel, and wild relatives. Findings reveal an expansion of ULP genes in cultivated rice, suggesting selection pressure during breeding and implicating specific ULPs in biotic and abiotic stress responses, providing resources for rice improvement.
The study shows that the membrane lipids PI4P, PI(4,5)P2, and phosphatidylserine have distinct spatial and temporal dynamics during lateral root primordium formation in Arabidopsis thaliana, with PI4P acting as a stable basal lipid, PI(4,5)P2 serving as a negative regulator of initiation, and phosphatidylserine increasing after founder cell activation. Using live-cell biosensors, genetic mutants, and an inducible PI(4,5)P2 depletion system, the authors demonstrate that reducing PI(4,5)P2 enhances lateral root initiation and development.
Researchers isolated a fungal pathogen from a naturally infected Rumex crispus leaf in Japan and identified it as Teratoramularia rumicicola using morphological traits and phylogenetic analysis of ITS and LSU rDNA sequences. Host range tests showed the isolate (TR4) caused disease and reduced biomass in three Rumex species but was harmless to five tested forage crops, indicating its potential as a selective bioherbicide for pasture systems.
Large-scale bioinformatics identified a new class of transmembrane phosphotransfer proteins (TM‑HPt) across 61 plant species, showing conserved HPt motifs and potential activity in multistep phosphorelay signaling. Phylogenetic relationships were inferred via Bayesian DNA analysis, expression was validated by transcriptomics, and molecular modeling suggested possible membrane-associated structural arrangements.
Gain and loss of gene function shaped the nickel hyperaccumulation trait in Noccaea caerulescens
Authors: Belloeil, C., Garcia de la Torre, V. S., Contreras Aguilera, R., Kupper, H., Lopez-Roques, C., Iampetro, C., Vandecasteele, C., Klopp, C., Launay-Avon, A., Leemhuis, W., Yamjabok, J., van den Heuvel, J., Aarts, M. G. M., Quintela Sabaris, C., Thomine, S., MERLOT, S.
The study presents a high-quality genome assembly for the nickel hyperaccumulator Noccaea caerulescens and uses it as a reference for comparative transcriptomic analyses across different N. caerulescens accessions and the non‑accumulating relative Microthlaspi perfoliatum. It identifies a limited set of metal transporters (NcHMA3, NcHMA4, NcIREG2, and NcIRT1) whose elevated expression correlates with hyperaccumulation, and demonstrates that frameshift mutations in NcIRT1 can abolish the trait, indicating an ancient, transporter‑driven origin of nickel hyperaccumulation.
The study identifies a novel C-terminal FR motif in Lotus japonicus NODULE INCEPTION (NIN) that expands DNA‑binding specificity by stabilizing the RWP‑RK dimer, and shows that loss of this motif impairs nodulation and nitrogen fixation. Comparative analysis reveals that Arabidopsis NLP2 also possesses a NIN‑type FR, and phylogenetic data suggest the motif originated in early gymnosperms, indicating it predates the evolution of root nodule symbiosis.
Mycotoxin-driven proteome remodeling reveals limited activation of Triticum aestivum responses to emerging chemotypes integrated with fungal modulation of ergosterols
Authors: Ramezanpour, S., Alijanimamaghani, N., McAlister, J. A., Hooker, D., Geddes-McAlister, J.
The study used comparative proteomics to examine how the emerging 15ADON/3ANX chemotype of Fusarium graminearum affects protein expression in both wheat and the fungus. It identified a core wheat proteome altered by infection, chemotype‑specific wheat proteins, and fungal proteins linked to virulence and ergosterol biosynthesis, revealing distinct molecular responses influencing disease severity.
MdBRC1 and MdFT2 Interaction Fine-Tunes Bud Break Regulation in Apple
Authors: Gioppato, H. A., Estevan, J., Al Bolbol, M., Soriano, A., Garighan, J., Jeong, K., Georget, C., Soto, D. G., El Khoury, S., Falavigna, V. d. S., George, S., Perales, M., Andres, F.
The study identifies the transcription factor MdBRC1 as a key inhibitor of bud growth during the ecodormancy phase in apple (Malus domestica), directly regulating dormancy‑associated genes and interacting with the flowering promoter MdFT2 to modulate bud break. Comparative transcriptomic analysis and gain‑of‑function experiments in poplar demonstrate that MdFT2 physically binds MdBRC1, attenuating its repressive activity and acting as a molecular switch for the transition to active growth.