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 study utilizes a large collection of fluorescently marked Ds-GFP insertional mutations in haploid maize pollen to link gene disruptions with quantitative fitness effects measured as transmission deviations. By integrating genome-derived features (e.g., codon usage) and expression profiling into interpretable machine learning models, they achieve high predictive performance (auROC >90%) for genes influencing pollen fitness, highlighting expression specificity as a key predictor.
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.
CYSTEINE-RICH RLK2 regulates development via callose synthase-dependent symplastic transport in Arabidopsis
Authors: Zeiner, A., Krasensky-Wrzaczek, J., Jindal, S., Hajny, J., Sharma, M., Morina, F., Andresen, E., Pääkkönen, M., Küpper, H., Merilahti, J., Wrzaczek, M.
The study reveals that Arabidopsis CRK2 phosphorylates the callose synthases CALS1 and CALS3, influencing callose deposition at plasmodesmata and thereby affecting phloem loading and source‑to‑sink transport. Loss of CRK2 leads to starch accumulation in older leaves, a phenotype rescued by introducing functional CALS1 or CALS3 alleles, indicating that CRK2, CALS1, and CALS3 jointly regulate growth and development through control of intercellular transport.
The study investigates the roles of the receptor-like kinase CRK2 and the RNA-binding protein GRP7 in regulating gibberellin signaling and floral transition in Arabidopsis, using phenotypic analyses of single and double mutants. Exogenous gibberellic acid treatments and transcript profiling reveal that CRK2 and GRP7 jointly modulate GA-responsive pathways, highlighting a novel regulatory layer involving membrane kinases and RNA-binding proteins.