The study investigates the gene regulatory network (GRN) controlling flowering time in the allotetraploid crop Brassica napus by comparing its transcriptome to that of Arabidopsis thaliana. While most orthologous gene pairs show conserved expression dynamics, several flowering‑time genes display regulatory divergence, especially under cold conditions, indicating subfunctionalisation among paralogues. Despite these differences, the overall GRN topology remains similar to Arabidopsis, likely due to retention of multiple paralogues.

The authors used a bottom‑up thermodynamic modelling framework to investigate how plants decode calcium signals, starting from Ca2+ binding to EF‑hand proteins and extending to higher‑order decoding modules. They identified six universal Ca2+-decoding modules that can explain variations in calcium sensitivity among kinases and provide a theoretical basis for interpreting calcium signal amplitude and frequency in plant cells.

The study genotyped 1,013 hard red spring wheat lines using SNP arrays and targeted KASP markers to track changes in genetic diversity and the distribution of dwarfing Rht alleles over a century of North American breeding. It found shifts from Rht‑D1b to Rht‑B1b dominance, identified low‑frequency dwarf alleles at Rht24 and Rht25 that have increased recently, and revealed gene interactions that can fine‑tune plant height, along with evidence of recent selection for photoperiod sensitivity.

The study generated a comprehensive transcriptome assembly for the macauba palm (Acrocomia aculeata) across seven distinct organs, annotating 42.85% of transcripts and identifying organ‑specific expression patterns. Comparative analyses revealed macauba‑unique gene families and numerous drought‑responsive genes, while root samples uncovered a notable presence of arbuscular mycorrhizal fungal transcripts, underscoring the importance of symbiotic interactions and stress signaling pathways.

A biparental Vicia faba mapping population was screened under glasshouse conditions for resistance to a mixture of Fusarium avenaceum and Fusarium oxysporum, revealing several families with moderate to high resistance. Using the Vfaba_v2 Axiom SNP array, a high-density linkage map of 6,755 SNPs was constructed, enabling the identification of a major QTL on linkage group 4 associated with partial resistance to foot and root rot.

The study demonstrates that RNA extracted from herbarium specimens can be used to generate high‑quality transcriptomes, comparable to those from fresh or silica‑dried samples. By assembling and comparing transcriptomes across specimen types, the authors validated a plant immune receptor synthesized from a 1956 collection, proving archival RNA’s utility for functional genomics. These findings challenge the prevailing view that herbarium RNA is unsuitable for transcriptomic analyses.