The study characterizes a conserved RNA structural element named DEAD within DEAD-box helicase genes in land plants, showing that it functions as a sensor of helicase activity to regulate alternative splicing in Arabidopsis thaliana. By modulating the folding of DEAD, the plant balances helicase transcript and protein levels via a negative feedback loop, and loss of this regulation leads to widespread splicing disruptions and severe stress phenotypes.

Field experiments combined with RNA sequencing revealed that wheat ploidy influences heat stress resilience, with tetraploid T. turgidum showing the smallest yield loss and hexaploid T. aestivum mounting the largest transcriptional response. Ploidy-dependent differences were observed in differential gene expression, alternative splicing—including hexaploid-specific exon skipping of NF‑YB—and co‑expression networks linked to grain traits, highlighting candidate pathways for breeding heat‑tolerant wheat.

The study used transcriptomic profiling to compare tomato (Solanum lycopersicum) responses to three evolutionarily distant pathogens—nematodes, aphids, and oomycetes—during compatible interactions, identifying differentially expressed genes and key host hubs. Integrating public datasets and performing co‑expression and GO enrichment analyses, the authors mapped shared dysregulation clusters and employed Arabidopsis interactome data to place tomato candidates within broader networks, highlighting potential targets for multi‑pathogen resistance.

The study generated the first tissue‑specific full‑length transcriptome atlas for Panax vietnamensis var. fuscidiscus using combined PacBio SMRT and Illumina RNA‑Seq, uncovering 281,468 transcripts and 8,089 novel genes. Twenty‑one candidate genes in triterpenoid saponin biosynthesis were identified, along with extensive alternative splicing events that appear to modulate tissue‑specific production of ocotillol‑type ginsenosides.

The study generated a dataset of 420 sgRNAs targeting promoters, exons, and introns of 137 tomato genes in protoplasts, linking editing efficiency to chromatin accessibility, genomic context, and sequence features. Open chromatin sites showed higher editing rates, while transcriptional activity had little effect, and a subset of guides produced near‑complete editing with microhomology‑mediated deletions. Human‑trained prediction models performed poorly, highlighting the need for plant‑specific guide design tools.

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 shows that nitrogen deficiency markedly elevates the exudation of the triterpenoid Solanoeclepin A (SolA) from tomato roots, a process that requires non‑sterile soil and involves the rhizosphere microbiota. Transient silencing of two candidate biosynthetic genes (CYP749A19 and CYP749A20) reduced SolA levels and impaired recruitment of beneficial Massilia spp., which promote plant growth under nitrogen limitation, indicating that SolA acts as a microbe‑mediated recruitment signal that was co‑opted by cyst nematodes.

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.