The study investigated how Arabidopsis thaliana SR protein kinases (AtSRPKs) regulate alternative RNA splicing by using chemical inhibitors of SRPK activity. Inhibition with SPHINX31 and SRPIN340 caused reduced root growth and loss of root hairs, accompanied by widespread changes in splicing and phosphorylation of genes linked to root development and other cellular processes. Multi‑omics analysis (transcriptomics and phosphoproteomics) revealed that AtSRPKs modulate diverse splicing factors and affect the splicing landscape of numerous pathways.

The study used TurboID-based proximity labeling coupled with mass spectrometry to map the Arabidopsis alternative splicing machinery centered on ACINUS, PININ, and SR45, identifying 298 high-confidence components and revealing that splicing is tightly linked to transcription and other RNA processing steps. Bioinformatic and genetic analyses, including O-glycosylation double mutants, demonstrated both conserved and plant‑specific regulatory networks and highlighted the role of sugar modifications in modulating splicing.

The study screened 6,274 elite rice genotypes for submergence and stagnant flooding tolerance, identifying 89 lines with superior performance, including 37 that outperformed SUB1A introgression lines by 40‑50%. These elite lines harbor 86 key QTLs/genes and were used in a novel Transition from Trait to Environment (TTE) breeding strategy, achieving a 65% genetic gain for submergence tolerance and demonstrating strong performance in flood‑prone regions of India and Bangladesh.

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 characterized 1,264 maize near‑isogenic lines derived from 18 donor inbreds crossed to the recurrent parent B73, using genotyping‑by‑sequencing and SNP‑chip data to detect 2,972 introgression segments via a novel hidden Markov model pipeline. Disease phenotyping enabled QTL mapping for foliar disease resistance, revealing extensive allelic variation among donor lines, and establishing the nNIL population as a valuable resource for dissecting complex traits in maize.

The study demonstrates that abscisic acid (ABA) accumulates in darkness to suppress cotyledon opening during seedling deetiolation, and that light exposure lifts this repression, enabling cotyledon aperture. Genome‑wide transcriptional and alternative‑splicing changes accompany this process, and the light‑dependent regulation requires the splicing factors RS40 and RS41, whose activity is repressed in the dark.