The study investigates the subfunctionalization of duplicated GIGANTEA paralogs in Petunia x hybrida, focusing on PhGI2's role in floral transition. While RNAi silencing of PhGI2 caused mixed vegetative and reproductive phenotypes, CRISPR/Cas9-generated loss‑of‑function alleles showed that PhGI2 specifically promotes flowering without affecting vegetative growth or scent. The findings reveal that PhGI2 is essential for maintaining circadian gene expression dynamics and regulating flowering time, separating vegetative growth from reproductive timing.

The study characterizes a conserved RNA structural element named DEAD within DEAD-box helicase genes in land plants, showing that it functions as a sensor of helicase activity to regulate alternative splicing in Arabidopsis thaliana. By modulating the folding of DEAD, the plant balances helicase transcript and protein levels via a negative feedback loop, and loss of this regulation leads to widespread splicing disruptions and severe stress phenotypes.

Field experiments combined with RNA sequencing revealed that wheat ploidy influences heat stress resilience, with tetraploid T. turgidum showing the smallest yield loss and hexaploid T. aestivum mounting the largest transcriptional response. Ploidy-dependent differences were observed in differential gene expression, alternative splicing—including hexaploid-specific exon skipping of NF‑YB—and co‑expression networks linked to grain traits, highlighting candidate pathways for breeding heat‑tolerant wheat.

The study generated the first tissue‑specific full‑length transcriptome atlas for Panax vietnamensis var. fuscidiscus using combined PacBio SMRT and Illumina RNA‑Seq, uncovering 281,468 transcripts and 8,089 novel genes. Twenty‑one candidate genes in triterpenoid saponin biosynthesis were identified, along with extensive alternative splicing events that appear to modulate tissue‑specific production of ocotillol‑type ginsenosides.

The study identified a heat‑responsive exon‑skipping event in the basic Helix‑Loop‑Helix domain of the transcription factor PIF4, which reduces PIF4 activity and promotes photomorphogenic traits in etiolated seedlings. This reveals a novel post‑transcriptional mechanism by which plants modulate PIF4 function during heat stress.

The study characterizes the plant spliceosomal protein AtSF1 in Arabidopsis thaliana, using iCLIP and RNA‑seq to map its in vivo branch point binding sites and demonstrate that loss of AtSF1 causes widespread 3' splice‑site mis‑selection. Structural comparison reveals a plant‑specific domain architecture, and the identified AtSF1 targets are enriched for circadian and defense genes, linking splicing regulation to timing and immunity.

The study identifies the serine/arginine-rich splicing factor RS2Z36 as a key regulator of ovary patterning and early fruit morphology in tomato, with loss‑of‑function mutants producing smaller, ellipsoid fruits and elongated pericarp cells. RNA‑seq and proteomic analyses reveal widespread alternative splicing and altered protein abundance, including novel splice‑variant peptides, while mutant pericarps show increased deposition of LM6‑detected arabinan and AGP epitopes.

The study functionally characterizes a conserved structured RNA motif (45ABC) in Arabidopsis RBP45 pre‑mRNAs, showing that its sequence and pairing elements mediate a negative auto‑ and cross‑regulatory feedback loop through alternative splicing that produces unproductive isoforms and reduces RBP45 expression. Transcriptome‑wide splicing analysis and phenotypic assessment of rbp45 mutants reveal that RBP45B plays a dominant role and that proper regulation of this motif is essential for root growth and flowering time.

The authors compiled and standardized published data on Rubisco dark inhibition for 157 flowering plant species, categorizing them into four inhibition levels and analyzing phylogenetic trends. Their meta‑analysis reveals a complex, uneven distribution of inhibition across taxa, suggesting underlying chloroplast microenvironment drivers and providing a new resource for future photosynthesis improvement efforts.

A large-scale proteomic study in Arabidopsis thaliana identified over 32,000 isoform-specific peptides, confirming that alternative splicing, particularly intron retention, produces translated protein isoforms. Integrated proteogenomic analysis, SUPPA classification, and AlphaFold modeling revealed structural impacts and a non-linear regulation of transcript and protein abundance, with mutant phenotypes linking splicing to growth, chlorophyll content, and anthocyanin accumulation.