The study investigates the molecular basis of heat‑tolerant pollen tube growth in tomato (Solanum lycopersicum) by comparing thermotolerant and sensitive cultivars. Using live imaging, transcriptomics, proteomics, and genetics, the authors identified the Rapid Alkalinization Factor (RALF) signaling pathway as a key regulator of pollen tube integrity under high temperature, with loss of a specific RALF peptide enhancing tube integrity in a thermotolerant cultivar.

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 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.

The study isolated an endophytic Pseudomonas aeruginosa strain (SPT08) from tomato cotyledon seedlings that suppressed the wilt pathogen Ralstonia pseudosolanacearum and promoted plant growth, increasing height by 20% and root biomass by 60%. GFP labeling confirmed endophytic colonization, and genomic analysis revealed multiple secretion systems and secondary‑metabolite gene clusters associated with biocontrol and growth‑promoting traits.

The study shows that the membrane lipids PI4P, PI(4,5)P2, and phosphatidylserine have distinct spatial and temporal dynamics during lateral root primordium formation in Arabidopsis thaliana, with PI4P acting as a stable basal lipid, PI(4,5)P2 serving as a negative regulator of initiation, and phosphatidylserine increasing after founder cell activation. Using live-cell biosensors, genetic mutants, and an inducible PI(4,5)P2 depletion system, the authors demonstrate that reducing PI(4,5)P2 enhances lateral root initiation and development.

The study integrates genome, transcriptome, and chromatin accessibility data from 380 soybean accessions to dissect the genetic and regulatory basis of symbiotic nitrogen fixation (SNF). Using GWAS, TWAS, eQTL mapping, and ATAC-seq, the authors identify key loci, co‑expression modules, and regulatory elements, and validate the circadian clock gene GmLHY1b as a negative regulator of nodulation via CRISPR and CUT&Tag. These resources illuminate SNF networks and provide a foundation for soybean improvement.

The study engineered the linear furanocoumarin pathway in tomato by integrating four biosynthetic genes, aiming to produce psoralen, but instead generated coumarins such as scopoletin. Morphophysiological, metabolomic, and transcriptomic analyses revealed that even low levels of these coumarins can influence plant growth and physiology, highlighting both benefits and costs of coumarin accumulation in crops.

The study investigates hormetic responses of tomato (Solanum lycopersicum) seedlings to low‑dose cadmium, demonstrating enhanced growth through morphological, biochemical, and histochemical analyses. Transcriptomic profiling revealed differential expression of oxidoreductase genes, signaling components, and several long non‑coding RNAs (lncRNAs) that generate miRNAs (sly‑MIR396a and sly‑MIR1063g), which modulate target genes to promote growth. In‑silico analyses of lncRNA targets and miRNA precursors provide mechanistic insight into cadmium‑induced hormesis and its potential for crop improvement.