The study uncovers how arbuscular mycorrhizal (AM) fungi induce lateral root formation in maize by activating ethylene‑responsive transcription factors (ERFs) that regulate pericycle cell division and reshape flavonoid metabolism, lowering inhibitory flavonols. It also shows that the rhizobacterium Massilia collaborates with AM fungi, degrading flavonoids and supplying auxin, thereby creating an integrated ethylene‑flavonoid‑microbe signaling network that can be harnessed to improve nutrient uptake and crop sustainability.

The complete chloroplast genome of the endemic fruit species Dillenia philippinensis was sequenced, assembled, and annotated, revealing a 161,591‑bp quadripartite structure with 113 unique genes. Comparative analyses identified simple sequence repeats, codon usage patterns, and phylogenetic placement close to D. suffroticosa, providing a genomic resource for future breeding and conservation efforts.

The authors compiled and standardized published data on Rubisco dark inhibition for 157 flowering plant species, categorizing them into four inhibition levels and analyzing phylogenetic trends. Their meta‑analysis reveals a complex, uneven distribution of inhibition across taxa, suggesting underlying chloroplast microenvironment drivers and providing a new resource for future photosynthesis improvement efforts.

The study engineered Tobacco rattle virus vectors incorporating distinct RNA secondary structures as mobility factors to improve guide RNA delivery to plant meristems. Using Nicotiana benthamiana plants expressing Cas9, optimal virus constructs were identified that generated both somatic and heritable edits, and these constructs were successfully applied to edit the emerging oilseed crop pennycress (Thlaspi arvense).

The authors introduce the ENABLE(R) Gene Editing in planta toolkit, a streamlined two‑step cloning system for creating CRISPR/Cas9 knockout vectors suitable for transient or stable transformation. Validation was performed in Oryza sativa protoplasts and Arabidopsis thaliana plants, and the toolkit includes low‑cost protocols aimed at facilitating adoption in the Global South.

The authors created a fast‑cycling, isogenic barley line (GP‑rapid) by introgressing the wild‑type Ppd‑H1 allele from Igri into the Golden Promise cultivar and performing two backcrosses to limit the donor genome, achieving a 25% reduction in generation time under speed‑breeding conditions while retaining high transformation efficiency. CRISPR/Cas9‑mediated editing of Ppd‑H1 showed regeneration and transformation rates comparable to the original Golden Promise, establishing GP‑rapid as a rapid platform for transgenic and gene‑edited barley research.

The study shows that inoculation with the non‑diazotrophic bacterium Enterobacter sp. SA187 significantly improves Arabidopsis thaliana growth under low nitrate conditions by increasing fresh weight, primary root length, and lateral root density, while enhancing nitrate accumulation and reducing shoot C:N ratios. Transcriptomic and mutant analyses reveal that these benefits depend on ethylene signaling and the activity of high‑affinity nitrate transporters NRT2.5 and NRT2.6, indicating an ethylene‑mediated, HATS‑dependent reprogramming of nitrogen uptake.

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.

The study reveals that Arabidopsis ethylene receptors ETR1 and ERS1 function as Ca²⁺-permeable channels, with ETR1 specifically mediating ethylene‑induced cytosolic Ca²⁺ spikes that influence hypocotyl elongation. Homologous receptors from diverse land plants and algae also show Ca²⁺ permeability, and ethylene further enhances this activity, indicating a conserved regulatory role across the green lineage.

The study demonstrates that ethylene signaling contributes to host resistance against the root parasitic plant Phelipanche aegyptiaca, as both water stress and parasitism activate ethylene responses in Arabidopsis roots. Application of the ethylene precursor ACC reduced parasite attachment, and mutants in ethylene signaling components (ETR1, CTR1) showed altered tolerance, highlighting ethylene-mediated defenses as a potential strategy for crop protection.