The study reveals that whole‑seedling transcriptomic analyses of Arabidopsis thermomorphogenesis are highly variable and often mask organ‑specific responses, with nearly 70% of differentially expressed genes in whole seedlings not detected in any dissected organ. By directly comparing RNA‑seq from whole seedlings and individual organs (root, hypocotyl, cotyledon) and supporting the findings with proteomics, the authors demonstrate that pooling tissues confounds gene‑regulation insights and call for organ‑level approaches in future warm‑temperature research.

The study characterized the virome of Tamarillo (Solanum betaceum) across eight locations in Narino, Colombia, revealing up to four virus species from the Torradovirus, Potyvirus, and Polerovirus genera, including the first report of a torradovirus in tamarillo. A novel isolate of potato virus Y‑Tamarillo (PVY‑Tam) with unique P3N‑PIPO protein truncations was identified, suggesting host‑specific adaptation and informing future diagnostic and control strategies.

The study used RNA‑seq to compare early transcriptional responses to acute heat and cold stress in cultivated cranberry (Vaccinium macrocarpon) and its F1 hybrids with the cold‑adapted wild relative V. oxycoccos. Cold stress triggered differential expression in pathways such as photosynthesis, ribosomes, defense, and hormone signaling, with some hybrids showing transiently elevated cold‑responsive expression, suggesting potential cold‑tolerance introgression. The results highlight the utility of wild germplasm for breeding temperature‑resilient cranberries.

The study investigated the molecular basis of quantitative resistance to black spot disease in a Rosa wichurana × Rosa chinensis F1 population, identifying two major QTLs (B3 on LG3 and B5 on LG5). RNA‑seq of inoculated and control leaf samples at 0, 3, and 5 days post‑inoculation revealed extensive transcriptional reprogramming, with QTL B3 triggering classic defense pathways and QTL B5 showing a limited, distinct response. These findings highlight complex, QTL‑specific regulation underlying durable black‑spot resistance in roses.

The study examines how the SnRK1 catalytic subunit KIN10 integrates carbon availability with root growth regulation in Arabidopsis thaliana. Loss of KIN10 reduces glucose‑induced inhibition of root elongation and triggers widespread transcriptional reprogramming of metabolic and hormonal pathways, notably affecting auxin and jasmonate signaling under sucrose supplementation. These findings highlight KIN10 as a central hub linking energy status to developmental and environmental cues in roots.

The study used phospho‑proteomics to uncover rapid phosphorylation changes in Arabidopsis seedlings upon light or sucrose exposure, identifying RS41 as a hyperphosphorylated SR protein. By creating single and higher‑order mutants of four RS genes, the authors demonstrated that these RS proteins are essential for photomorphogenic development and regulate light‑dependent alternative splicing, with loss of all four causing sterility.

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 identified key transcription factors governing the development of T-shaped non-glandular trichomes (TSTs) in Artemisia argyi by comparing RNA‑seq profiles of TST‑bearing and non‑TST tissue, highlighting the AarMIXTA gene family as central regulators. Overexpressing AarMIXTA1.2 in transgenic Arabidopsis thaliana markedly increased TST density, suggesting a positive regulatory role of these MIXTA genes in trichome formation and providing insights for high‑yield moxa floss cultivation.

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.