The study investigates the evolutionary shift from archegonial to embryo‑sac reproduction by analyzing transcriptomes of Ginkgo reproductive organs and related species. It reveals that the angiosperm pollen‑tube guidance module MYB98‑CRP‑ECS is active in mature Ginkgo archegonia and that, while egg cell transcription is conserved, changes in the fate of other female gametophyte cells drove the transition, providing a molecular framework for this major reproductive evolution.

The study used multi‑season phenotyping for iron, zinc, and protein content together with whole‑genome re‑sequencing of a groundnut mini‑core collection to conduct a genome‑wide association study, identifying numerous marker‑trait associations and candidate genes linked to nutrient homeostasis. SNP‑based KASP markers were designed for nine loci, of which three showed polymorphism and are ready for deployment in genomics‑assisted breeding for nutrient‑rich groundnut varieties.

The study profiled small interfering RNAs (siRNAs) in barley (Hordeum vulgare) seeds differing in viability after controlled long‑term storage, identifying 85,728 differentially expressed siRNAs associated with seed vigor. Trans‑acting siRNAs displayed distinct temporal patterns during imbibition, and functional analyses linked siRNA targets to key processes such as cytochrome activity, root development, and carbohydrate metabolism, suggesting a role in maintaining metabolic activity during germination.

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 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 demonstrates that in barley (Hordeum vulgare) the MAPK pathway, specifically the MKK3 kinase, controls grain dormancy through a combination of haplotype variation, copy-number changes, and intrinsic kinase activity. Historical selection of particular MKK3 haplotypes correlates with climatic pressures, offering a genetic basis to balance short dormancy with resistance to pre‑harvest sprouting under climate change.

The study generated a phenotypic dataset for 550 Lactuca accessions, including 20 wild relatives, and applied an iterative two‑step GWAS using a jointly processed SNP set for cultivated lettuce (L. sativa) and its wild progenitor (L. serriola) to dissect trait loci. Known and novel QTLs for anthocyanin accumulation, leaf morphology, and pathogen resistance were identified, with several L. serriola‑specific QTLs revealing unique genetic architectures, underscoring the breeding value of wild lettuce species.

The study used chlorophyll fluorescence imaging to map non-photochemical quenching (NPQ) gradients along barley leaf axes and found heat stress attenuates NPQ induction, revealing spatial heterogeneity in stress responses. Genome‑wide association and transcriptomic analyses identified candidate genes, notably HORVU.MOREX.r3.3HG0262630, that mediate region‑specific heat responses, highlighting pathways for improving cereal heat resilience.

The study identifies the transcription factor MdBRC1 as a key inhibitor of bud growth during the ecodormancy phase in apple (Malus domestica), directly regulating dormancy‑associated genes and interacting with the flowering promoter MdFT2 to modulate bud break. Comparative transcriptomic analysis and gain‑of‑function experiments in poplar demonstrate that MdFT2 physically binds MdBRC1, attenuating its repressive activity and acting as a molecular switch for the transition to active growth.

The study introduced full-length SOC1 genes from maize and soybean, and a partial SOC1 gene from blueberry, into tomato plants under constitutive promoters. While VcSOC1K and ZmSOC1 accelerated flowering, all three transgenes increased fruit number per plant mainly by promoting branching, and transcriptomic profiling revealed alterations in flowering, growth, and stress‑response pathways.