The study examined how the bioinoculant Trichoderma afroharzianum T22 influences Pisum sativum growth under iron-sufficient versus iron-deficient conditions, finding pronounced benefits—enhanced photosynthesis, Fe/N accumulation, and stress‑related gene expression—only during iron deficiency. RNA‑seq revealed distinct gene expression patterns tied to symbiosis, iron transport, and redox pathways, and microbiome profiling showed T22 reshapes the root bacterial community under deficiency, suggesting context‑dependent mutualism.

The study characterizes tissue-specific elimination of B chromosomes in Sorghum purpureosericeum during embryo development, identifying 28 candidate genes linked to this process. Integrated in situ visualization, genome sequencing, and transcriptomic analyses reveal that the B chromosome originates from multiple A chromosomes, harbors unique repeats, and expresses divergent kinetochore components that likely mediate its selective removal.

The study evaluated whether integrating genomic, transcriptomic, and drone-derived phenomic data improves prediction of 129 maize traits across nine environments, using both linear (rrBLUP) and nonlinear (SVR) models. Multi-omics models consistently outperformed single-omics models, with transcriptomic data especially enhancing cross‑environment predictions and capturing genotype‑by‑environment interactions. The results highlight the added value of combining transcriptomics and phenomics with genotypes for more accurate and generalizable trait prediction in maize.

The study identified a major QTL on chromosome 6A that accounts for 40% of variation in medium-chain ester (MCE) levels in strawberry fruit, pinpointing FaCCR1 and FaOCT4 as the causal genes. Functional validation through subcellular localization, transient overexpression, enzymatic assays, and molecular docking demonstrated that FaCCR1 also catalyzes MCE precursor reactions, and a KASP marker in FaOCT4 was developed for breeding fragrant cultivars.

Phytoplasma infection in sesame (Sesamum indicum) triggers tissue-specific alterations in gene expression and metabolite composition, with floral organs adopting leaf-like traits and distinct changes in porphyrin, brassinosteroid, and phenylpropanoid pathways. Integrated transcriptomic and metabolomic analyses, supported by biochemical, histological, and qRT-PCR assays, reveal differential stress and secondary metabolite responses between infected leaves and flowers.

The study provides a comprehensive proteomic analysis of seed mitochondria from white lupin, revealing fully assembled OXPHOS complexes ready for immediate energy production upon imbibition. Quantitative mass‑spectrometry identified 1,162 mitochondrial proteins, highlighting tissue‑specific transporter and dehydrogenase profiles and dynamic remodeling during early germination, while many uncharacterized proteins suggest novel legume‑specific functions.

The study examined how prior light‑acclimation influences the fitness and rapid photoprotective reprogramming of Chlamydomonas during transitions between low and high diurnal light intensities. While high‑light‑acclimated cells struggled to grow and complete the cell cycle after shifting to low light, low‑light‑acclimated cells quickly remodeled thylakoid ultrastructure, enhanced photoprotective quenching, and altered photosystem protein levels, recovering chloroplast function within a single day. Transcriptomic and proteomic profiling revealed swift induction of stress‑response genes, indicating high flexibility in diurnal light acclimation.

The study presents an optimized Agrobacterium-mediated transformation protocol for bread wheat that incorporates a GRF4‑GIF1 fusion to enhance regeneration and achieve genotype‑independent transformation across multiple cultivars. The approach consistently improves transformation efficiency while limiting pleiotropic effects, offering a versatile platform for functional genomics and gene editing in wheat.

The study introduces a native‑condition method combining cell fractionation and immuno‑isolation to purify autophagic compartments from Arabidopsis, followed by proteomic and lipidomic characterisation of the isolated phagophore membranes. Proteomic profiling identified candidate proteins linked to autophagy, membrane remodeling, vesicular trafficking and lipid metabolism, while lipidomics revealed a predominance of glycerophospholipids, especially phosphatidylcholine and phosphatidylglycerol, defining the unique composition of plant phagophores.

The study identified seven adult plant resistance QTL for oat crown rust using two recombinant inbred line populations, with a major QTL (QPc_GS7_4A.2) on chromosome 4A closely linked to the Pc61 resistance gene. KASP markers targeting SNPs tightly linked to the four most significant QTL were developed, and genetic and haplotype analyses confirmed the association of QPc_GS7_4A.2 with both seedling and adult plant resistance, providing valuable tools for oat breeding.