The study applied limited proteolysis‑coupled mass spectrometry (LiP‑MS) to map JA‑protein interactions, validating known JA binders and uncovering novel candidates, including several UDP‑glucuronosyltransferases (UGTs). Functional omics, biochemical, enzymatic, and structural analyses demonstrated that two tomato UGTs glucosylate jasmonic acid, revealing a previously missing step in JA catabolism.

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.

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 assessed the impact of adding mammalian growth factors and cytokines to transformation media on CRISPR‑Cas9–mediated genome editing in six tomato (Solanum lycopersicum) accessions with varying regeneration capacities. Over three years, supplementation with these factors significantly increased regeneration rates and the production of stable secondary transgenic lines, especially in recalcitrant genotypes.

The researchers created tomato lines overexpressing the autophagy gene SlATG8f and evaluated their performance under high-temperature stress. qRT‑PCR and physiological measurements revealed that SlATG8f overexpression enhances expression of autophagy‑related and heat‑shock protein genes, accelerates fruit ripening, and improves fruit quality under heat stress.

Proteomic comparison of mock‑ and potato spindle tuber viroid‑infected tomato revealed a broad down‑regulation of nucleoporins and nuclear transport receptors, leading to impaired nuclear import of the immune regulator NPR1. Overexpression of NPR1 or treatment with a salicylic‑acid analog restored defense and reduced PSTVd infection, highlighting nuclear transport repression as a key vulnerability in plant immunity against viroids.

Regenerative agriculture using a grass-clover ley increased wheat yields and macroaggregate stability despite reduced root biomass, but did not enhance soil carbon sequestration as measured by 14C retention. Drought further decreased photosynthate allocation to roots, especially in ley soils, while genotype effects on yield were minimal.

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.