The study characterizes a radiation‑induced root‑suppressed (Rs) mutant in tomato that displays dwarfism and pleiotropic defects in leaves, flowers, and fruits. Metabolite profiling and rescue with H2S donors implicate disrupted sulfur metabolism, and whole‑genome sequencing identifies promoter mutations in two root‑meristem‑specific sulfotransferase genes as likely contributors to the root phenotype.

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 study identified a heat‑responsive exon‑skipping event in the basic Helix‑Loop‑Helix domain of the transcription factor PIF4, which reduces PIF4 activity and promotes photomorphogenic traits in etiolated seedlings. This reveals a novel post‑transcriptional mechanism by which plants modulate PIF4 function during heat stress.

The study characterizes the plant spliceosomal protein AtSF1 in Arabidopsis thaliana, using iCLIP and RNA‑seq to map its in vivo branch point binding sites and demonstrate that loss of AtSF1 causes widespread 3' splice‑site mis‑selection. Structural comparison reveals a plant‑specific domain architecture, and the identified AtSF1 targets are enriched for circadian and defense genes, linking splicing regulation to timing and immunity.

The authors used a bottom‑up thermodynamic modelling framework to investigate how plants decode calcium signals, starting from Ca2+ binding to EF‑hand proteins and extending to higher‑order decoding modules. They identified six universal Ca2+-decoding modules that can explain variations in calcium sensitivity among kinases and provide a theoretical basis for interpreting calcium signal amplitude and frequency in plant cells.

The study identifies two diel regulatory modules that coordinate plant cuticle formation: the LRB‑phyB‑PIF4 pathway suppresses wax biosynthesis during daylight, while the COP1‑CFLAP1 pathway promotes cutin accumulation at night. Degradation of phyB and CFLAP1 via specific E3 ubiquitin ligases modulates the activity of transcription factors PIF4 and BDG1 to ensure timely cuticle assembly.

The study shows that high ambient temperature triggers extensive changes in ROS homeostasis in Arabidopsis seedlings, with H2O2 balance being essential for thermomorphogenic hypocotyl elongation. PIF4 directly activates catalase genes CAT2 and CAT3 to regulate H2O2 levels, forming a PIF4‑CAT‑H2O2 module that operates alongside the PIF4‑auxin pathway, while elevated H2O2 feeds back to reduce PIF4 protein abundance.

The study profiled root transcriptomes of Arabidopsis wild type and etr1 gain-of-function (etr1-3) and loss-of-function (etr1-7) mutants under ethylene or ACC treatment, identifying 4,522 ethylene‑responsive transcripts, including 553 that depend on ETR1 activity. ETR1‑dependent genes encompassed ethylene biosynthesis enzymes (ACO2, ACO3) and transcription factors, whose expression was further examined in an ein3eil1 background, revealing that both ETR1 and EIN3/EIL1 pathways regulate parts of the network controlling root hair proliferation and lateral root formation.

The study investigated how Arabidopsis thaliana SR protein kinases (AtSRPKs) regulate alternative RNA splicing by using chemical inhibitors of SRPK activity. Inhibition with SPHINX31 and SRPIN340 caused reduced root growth and loss of root hairs, accompanied by widespread changes in splicing and phosphorylation of genes linked to root development and other cellular processes. Multi‑omics analysis (transcriptomics and phosphoproteomics) revealed that AtSRPKs modulate diverse splicing factors and affect the splicing landscape of numerous pathways.

The study demonstrates that the microtubule‑associated protein WDL4 is essential for PhyB‑dependent thermomorphogenic and photomorphogenic responses in Arabidopsis, as wdl4-3 mutants mimic phyB loss‑of‑function phenotypes under varying temperatures and light conditions. Genetic analyses reveal that PIF4 activity is required for wdl4-3 hypocotyl hyper‑elongation, and while exogenous auxin can rescue pif4‑related defects, it does not restore the wdl4-3 specific elongation, indicating additional regulatory layers.