The study identified lineage-specific long non‑coding RNAs (lncRNAs) from the aphid‑specific Ya gene family in Rhopalosiphum maidis and R. padi, demonstrating that these Ya lncRNAs are secreted into maize, remain stable, and move systemically. RNA interference of Ya genes reduced aphid fecundity, while ectopic expression of Ya lncRNAs in maize enhanced aphid colonization, indicating that Ya lncRNAs act as cross‑kingdom effectors that influence aphid virulence.

The study characterizes insertion mutants of the Arabidopsis thaliana CKL12 kinase, revealing its role in hypocotyl and primary root growth and indicating that the 3' end of its transcript is crucial for function. Evidence suggests CKL12 is transcriptionally regulated by brassinosteroid signaling, as its promoter binds BR-related transcription factors and their RNAi-mediated knock‑down reduces CKL12 expression, placing CKL12 downstream of BR signaling in seedling development.

The study identified seven adult plant resistance QTL for oat crown rust using two recombinant inbred line populations, with a major QTL (QPc_GS7_4A.2) on chromosome 4A closely linked to the Pc61 resistance gene. KASP markers targeting SNPs tightly linked to the four most significant QTL were developed, and genetic and haplotype analyses confirmed the association of QPc_GS7_4A.2 with both seedling and adult plant resistance, providing valuable tools for oat breeding.

The study identifies the brown planthopper salivary protein NlAnnexin-like5 (NlANX5) as a key virulence effector that disrupts rice annexin (OsANN) function, leading to altered calcium signaling and reduced plant resistance. RNAi silencing of NlANX5 impairs BPH feeding, while transgenic rice overexpressing OsANN2/OsANN8 or NlANX5 restores resistance, demonstrating an anti‑virulence breeding strategy for rice.

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 investigates the genetic basis of sex determination in Cannabis sativa, identifying a X‑chromosome locus (Monoecy1) that governs the switch between dioecy and monoecy. Transcriptomic and genomic analyses reveal three tightly linked genes with sex‑specific expression, suggesting their combined action controls both flower type and individual sex phenotype.

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.

The study validates and quantifies biological nitrogen fixation in Mexican maize varieties and assesses a double‑haploid population derived from an elite inbred (PHZ51) crossed with these landraces. Aerial root traits show moderate to high heritability, and QTL mapping reveals multiple loci influencing root number, node occurrence, and diameter, with most favorable alleles originating from the landraces. The authors suggest that pyramiding the identified QTL into elite germplasm could enhance maize’s BNF capacity, pending field validation.

The study used QTL mapping in two F1 Plasmopara viticola populations to locate avirulence genes linked to grapevine resistance loci Rpv3.1, Rpv10, and Rpv12, confirming AvrRpv3.1 and identifying AvrRpv12, which harbors large deletions of RXLR effector genes. Additionally, a dominant locus responsible for partial Rpv10 breakdown was discovered, revealing diverse evolutionary mechanisms—including structural rearrangements and admixture—that enable the pathogen to overcome host resistance.