The study investigates the gene regulatory network (GRN) controlling flowering time in the allotetraploid crop Brassica napus by comparing its transcriptome to that of Arabidopsis thaliana. While most orthologous gene pairs show conserved expression dynamics, several flowering‑time genes display regulatory divergence, especially under cold conditions, indicating subfunctionalisation among paralogues. Despite these differences, the overall GRN topology remains similar to Arabidopsis, likely due to retention of multiple paralogues.

The study characterizes a novel variegated barley mutant whose phenotype results from duplicate dominant epistasis, representing the first documented digenic control in chloroplast-deficient mutants. Whole-genome resequencing mapped the causative loci Var4 and Var5 to chromosomes 2H and 3H, identifying an NBR1-like autophagy receptor and a DNAJ-domain protein as candidate genes involved in chloroplast proteostasis. The authors propose that combined mild proteostasis defects from each mutation exceed a functional threshold, disrupting early chloroplast development while allowing later recovery.

The study cloned the resistance genes Rmo2 and Rwt7 from barley and wheat, revealing them as orthologous tandem kinase proteins (TKPs) with an N‑terminal heavy metal‑associated (HMA) domain. Domain‑swapping experiments indicated that the HMA domain dictates effector specificity, supporting a model of TKP diversification into paralogs and orthologs that recognize distinct pathogen effectors.

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.

Four barley genotypes were examined under simultaneous Fusarium culmorum infection and drought, revealing genotype-dependent Fusarium Head Blight severity and largely additive transcriptomic responses dominated by drought. Co‑expression and hormone profiling linked ABA and auxin to stress‑specific gene modules, and a multiple linear regression model accurately predicted combined‑stress gene expression from single‑stress data, suggesting modular regulation.

The study used comparative transcriptomics of dorsal and ventral petals across development, alongside expression profiling in floral symmetry mutants, to identify genes linked to dorsal (AmCYC-dependent) and ventral (AmDIV-dependent) identities in Antirrhinum majus. In situ hybridisation validated axis‑specific and boundary‑localized expression patterns, revealing that a conserved NGATHA‑LIKE1‑BRASSINAZOLE‑RESISTANT1‑miR164 module has been co‑opted to regulate AmDIV targets and shape the corolla. These findings delineate regulatory modules coordinating dorsoventral and proximal‑distal patterning in zygomorphic flowers.

The study used ft1 knock‑out mutants in barley to demonstrate that the florigen homolog FT1 links vegetative and reproductive meristem development with plant metabolism, influencing source‑sink dynamics, longevity, and fertility. Loss of FT1 caused altered leaf and inflorescence determinacy, increased organ size but reduced fertility, and a transcriptional shift toward photosynthetic and carbon‑catabolism genes, while soluble sugar and starch accumulated in inflorescences, indicating diminished sink strength.

The study sequenced genomes of ericoid mycorrhiza‑forming liverworts and experimentally reconstituted the symbiosis, revealing a nutrient‑regulated state that supports intracellular colonization. Comparative transcriptomics identified an ancestral gene module governing intracellular symbiosis, and functional validation in Marchantia paleacea through genetic manipulation, phylogenetics, and transactivation assays confirmed its essential role. The findings suggest plants have retained and independently recruited this ancestral module for diverse intracellular symbioses.

The study benchmarked several sampling approaches for simultaneous profiling of root exudates and rhizosphere microbiota in soil-grown barley, revealing consistent exudate chemistry across methods but variation in root morphology and nitrogen exudation. High‑throughput amplicon sequencing and quantitative PCR showed protocol‑specific impacts on microbial composition, yet most rhizosphere-enriched microbes were captured by all approaches. The authors conclude that different protocols provide comparable integrated data, though methodological differences must be aligned with experimental objectives.

The study examined how allelic variation at three barley flowering-time genes (PPD‑H1, ELF3, and PHYC) influences photoperiod response parameters, revealing that ELF3 reduces intrinsic earliness and PhyC‑e lowers photoperiod sensitivity. By testing Near Isogenic Lines and HEB‑25 lines under 16–24 h photoperiods, the authors identified a 20‑h threshold for PPD‑H1 lines and proposed reduced photoperiod regimes (20 h and 16 h) for energy‑efficient speed breeding.