The study applied CRISPR/Cas9 gene editing to Physalis peruviana to modify plant‑architecture genes and create a compact growth ideotype. This compact phenotype is intended to increase per‑plot yield and support future breeding efforts for this nutritionally valuable minor crop.

RNA sequencing of the halophyte Salicornia europaea revealed that combined hypoxia‑salt stress triggers a unique transcriptional response, with 16% of genes specifically altered and distinct synergistic, antagonistic, and additive effects across functional pathways. Metabolic analyses indicated enhanced sucrose and trehalose metabolism, a shift toward lactate fermentation, and increased proline synthesis, highlighting complex regulatory strategies for coping with concurrent stresses.

In a controlled dry-down experiment, Arabis sagittata showed significantly higher recovery from drought than the endangered Arabis nemorensis, a difference that could not be traced to a single major QTL, indicating a polygenic basis. Transcriptome and small‑RNA sequencing revealed that A. sagittata mounts a stronger transcriptional response, including species‑specific regulation of the conserved drought miRNA miR408, and machine‑learning identified distinct cis‑regulatory motif patterns underlying these divergent stress‑response networks.

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.

The study examined whether colonisation by the arbuscular mycorrhizal fungus Rhizophagus irregularis primes immune responses in barley against the leaf rust pathogen Puccinia hordei. While AMF did not affect disease severity or plant growth, co‑infected leaves showed heightened expression of defence genes and transcriptome reprogramming, including altered protein ubiquitination, indicating a priming mechanism. These results highlight transcriptional and post‑translational pathways through which AMF can enhance barley disease resistance for sustainable crop protection.

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 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 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 characterizes telomere repeat binding (TRB) proteins in the model moss Physcomitrium patens, demonstrating that individual PpTRB genes are essential for normal protonemal and gametophore development and that loss of TRBs leads to telomere shortening, mirroring findings in seed plants. Transcriptome analysis of TRB mutants shows altered expression of genes linked to transcription regulation and stimulus response, while subcellular localization confirms nuclear residence and mutual interaction of PpTRBs, underscoring their conserved role in telomere maintenance across land plants.

The study introduces a CRISPR/Cas9‑based restoration system (CiRBS) that reactivates a disabled luciferase reporter (LUC40Ins26bp) in transgenic Arabidopsis, enabling long‑term single‑cell bioluminescence monitoring. Restoration occurs within 24 h after particle‑bombardment‑mediated CRISPR delivery, with ~7 % of cells regaining luminescence and most restored cells carrying a single correctly edited chromosome, facilitating reliable analysis of cellular gene‑expression heterogeneity.