Genetius

The study maps the in vivo proximity interactome of Arabidopsis SKP1-LIKE 1 (ASK1) under acute abscisic acid (ABA) signaling and prolonged drought using TurboID-based proximity labeling and quantitative proteomics, revealing condition-specific networks that include both canonical SCF modules and diverse noncanonical partners. Overexpression of ASK1 shifts proteome composition toward drought‑protective and ABA‑responsive proteins while repressing immune and ROS‑scavenging pathways, highlighting ASK1 as a hub that integrates SCF‑dependent and independent pathways to reprogram transcription, translation, and proteostasis during stress adaptation.

The study introduced charge-altering mutations into the N‑terminal region of Lhcb2 in Arabidopsis thaliana lacking native Lhcb2 to assess how intrinsic charge affects LHCII phosphorylation, state‑transition efficiency, and PSI‑LHCII complex formation. The R2E mutation drastically reduced Lhcb1/2 phosphorylation, impaired state transitions, and prevented PSI‑LHCII assembly, whereas the Q9E mutation had no measurable impact, and neither mutation altered thylakoid ultrastructure. Residual state transitions in the R2E line suggest that other Stn7 substrates can partially compensate for the loss of Lhcb2 phosphorylation.

Arabidopsis pub41 mutants display reduced root hair number and length, while auxin up‑regulates PUB41 transcript and protein levels. A catalytically inactive PUB41ΔU construct rescues the mutant phenotype and makes plants hyper‑responsive to auxin, localizing preferentially to trichoblasts and colocalizing with the auxin exporter PIN2. Biochemical and microscopy analyses reveal that PUB41 physically interacts with the cytoplasmic loop of PIN2, stabilizing its abundance, indicating that PUB41 modulates root hair development through PIN2 regulation.

The study presents near‑atomic cryo‑EM structures of the Arabidopsis receptor kinase HSL3 bound to the cyclic peptide CTNIP4, revealing a two‑step electrostatic steering and motif anchoring mechanism that involves a critical N‑glycan contact. Structure‑guided mutagenesis and ROS burst assays confirm the functional relevance of the identified binding interfaces, while truncation analyses define the minimal active peptide region for stress signaling.

Arabidopsis GAUT1 homozygous mutants display severe dwarfism, reduced cell size, and altered pollen tube growth, which is rescued by GAUT1 complementation. Cell‑wall analyses reveal a ~30% reduction in galacturonic acid, specifically loss of tightly bound homogalacturonan associated with RG‑II in the 4 M KOH post‑chlorite fraction, and super‑resolution microscopy shows diminished HG nanofilaments, indicating that GAUT1‑derived HG is essential for RG‑II‑containing polymers and seedling cell expansion.

The study uncovers that the Arabidopsis protein CDM1 regulates translation of meiotic transcripts by forming dynamic cytoplasmic condensates that associate with processing bodies and stress granules. CDM1 binds prophase I mRNAs, repressing their translation until later meiotic stages, and its loss disrupts chromosome pairing, condensation, and cytokinesis during microsporogenesis.

The study reveals that salt stress dynamically regulates REMORIN family genes, with REM1.2 rapidly relocalizing into static plasma membrane nanodomains that co‑localize with the actin-nucleating protein FORMIN 6. Overexpression of REM1.2 impairs early salt signaling and cell morphological adaptations, leading to heightened salt sensitivity, linking REMORIN nanodomains to both biotic and abiotic signaling pathways.

The study identifies members of the REMORIN protein family as inhibitors of plasma membrane H⁺‑ATPases, leading to extracellular pH alkalinization that modulates cell surface processes such as steroid hormone signaling and coordinates root developmental transitions in Arabidopsis thaliana. This inhibition represents an ancient mechanism predating root evolution, suggesting that extracellular pH patterning has shaped plant morphogenesis.

The abstract proposes that microbial indole-3-acetic acid (IAA) enhances plant thermotolerance by regulating proline metabolism, coordinating early osmoprotective synthesis with later catabolism to support growth and redox balance during heat stress. This regulation is hypothesized to involve integration of auxin perception (HSP90‑TIR1), MAPK signaling (MPK‑IAA8), mitochondrial redox components (SSR1, HSCA2) and interactions with abscisic acid and ethylene, offering a framework for using auxin‑producing microbes to boost heat resilience.

Parallel quantitative proteome and transcriptome time‑course profiling of Arabidopsis thaliana revealed that circadian clock genes, especially the morning‑expressed LHY/CCA1 module, exert extensive control over diel proteome rhythmicity, far exceeding their impact on the transcriptome. This control creates a bimodal phase distribution of rhythmic proteins that is lost in clock‑deficient mutants, indicating pervasive post‑translational regulation of gene expression by the circadian system.