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.

In a two-year controlled-environment experiment, diploid and tetraploid individuals of wild-type and cultivar Marshall annual ryegrass (Lolium multiflorum) were grown under elevated CO2 (540 vs 800 ppm) and differing evapotranspiration regimes. Elevated CO2 increased total biomass by 44% across ploidy levels, and tetraploid wild-type plants matched the improved cultivar in growth and forage quality, indicating that chromosome manipulation and wild genetic resources can enhance climate resilience.

The study examined how polyploidy, hybridization, and incomplete lineage sorting affect phylogenetic reconstructions in the genus Packera, evaluating several published paralog‑processing pipelines. Results showed that the choice of orthology and paralog handling methods markedly altered tree topology, time‑calibrated phylogenies, biogeographic histories, and detection of ancient reticulation, underscoring the need for careful methodological selection alongside comprehensive taxon sampling.

The study developed a molecular assay to identify Myrtle rust‑resistant Melaleuca quinquenervia individuals for restoration. Artificial inoculations were followed by whole‑genome sequencing of 492 seedlings and a GWAS that pinpointed SNP clusters in three chromosomal regions, including candidate R‑genes, which were refined into a 1,049‑SNP panel achieving a genomic prediction accuracy of R = 0.83.

The study integrated weekly morphophysiological measurements with high-density genotyping-by-sequencing data and a machine‑learning pipeline to dissect flowering time variation in diverse Cannabis sativa landraces. By applying mutual information, recursive feature elimination, random forest, and support vector machine classifiers to over 234,000 combined genetic, phenotypic, and environmental features, the authors identified 53 key markers that classify early, medium, and late flowering types with 96.6% accuracy. Notable loci, including CsFT3 and CsCFL1, were highlighted as promising targets for breeding and smart‑crop strategies.

The study used multi‑season phenotyping for iron, zinc, and protein content together with whole‑genome re‑sequencing of a groundnut mini‑core collection to conduct a genome‑wide association study, identifying numerous marker‑trait associations and candidate genes linked to nutrient homeostasis. SNP‑based KASP markers were designed for nine loci, of which three showed polymorphism and are ready for deployment in genomics‑assisted breeding for nutrient‑rich groundnut varieties.

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 identified a major QTL (qDTH3) on chromosome 3 responsible for a 7‑10‑day earlier heading phenotype in the rice line SM93, using QTL‑seq, KASP genotyping, association mapping, and transcriptomic analysis to fine‑map the locus to a 2.53 Mb region and pinpoint candidate genes. SNP markers linked to these genes were proposed as tools for breeding early‑maturing, climate‑resilient rice varieties.

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.