The study used CRISPR/Cas9 to edit the downstream region of the Arabidopsis thaliana FLOWERING LOCUS T (FT) gene, identifying a 2.3‑kb segment containing the Block E enhancer as crucial for normal FT expression and flowering. Fine‑scale deletions pinpointed a 63‑bp core module with CCAAT‑ and G‑boxes, and revealed a cryptic CCAAT‑box that becomes active when repositioned, highlighting the importance of local chromatin context and motif arrangement for enhancer function.

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 optimized three wheat transformation methods—immature embryo, callus, and in planta injection—by systematically adjusting Agrobacterium strain, bacterial density, acetosyringone concentration, and incubation conditions, achieving transformation efficiencies up to 66.84%. Using these protocols, CRISPR/Cas9 knockout of the negative regulator TaARE1-D produced mutants with increased grain number, spike length, grain size, and a stay‑green phenotype, demonstrating the platform’s potential to accelerate yield and stress‑tolerance improvements in wheat.

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 authors introduced a polycistronic tRNA‑gRNA array for CRISPR/Cas9 editing in Physcomitrium patens that doubled the frequency of large, targeted deletions compared with conventional single‑gRNA constructs. Using dual‑gRNA targeting, they achieved simultaneous deletion of two to four genes (katanin and TPX2 families) in a single transformation, reaching up to 42% efficiency per gene, though efficiency depended on gRNA pair design.

The study presents a high-quality genome assembly for the nickel hyperaccumulator Noccaea caerulescens and uses it as a reference for comparative transcriptomic analyses across different N. caerulescens accessions and the non‑accumulating relative Microthlaspi perfoliatum. It identifies a limited set of metal transporters (NcHMA3, NcHMA4, NcIREG2, and NcIRT1) whose elevated expression correlates with hyperaccumulation, and demonstrates that frameshift mutations in NcIRT1 can abolish the trait, indicating an ancient, transporter‑driven origin of nickel hyperaccumulation.

The study used CRISPR/Cas9 to generate rice snrk1 mutants and performed integrated phenotypic, transcriptomic, proteomic, and phosphoproteomic analyses under normal and starvation conditions, revealing SnRK1’s dual role in promoting growth and mediating stress responses. Findings indicate sub-functionalization of SnRK1 subunits and identify novel phosphorylation targets linked to membrane trafficking, ethylene signaling, and ion transport.

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.

Foliar application of Trichoderma harzianum cell‑free culture filtrates (CF) increased fruit yield, root growth, and photosynthesis in a commercial tomato cultivar under prolonged water deficit in a Mediterranean greenhouse. Integrated physiological, metabolite, and transcriptomic analyses revealed that CF mitigated drought‑induced changes, suppressing about half of water‑stress responsive genes, thereby reducing the plant’s transcriptional sensitivity to water scarcity.