Tomato leaf transcriptomic changes promoted by long-term water scarcity stress can be largely prevented by a fungal-based biostimulant
Authors: Lopez-Serrano, L., Ferez-Gomez, A., Romero-Aranda, R., Jaime Fernandez, E., Leal Lopez, J., Fernandez Baroja, E., Almagro, G., Dolezal, K., Novak, O., Diaz, L., Bautista, R., Leon Morcillo, R. J., Pozueta Romero, J.
Foliar application of Trichoderma harzianum cell‑free culture filtrates (CF) increased fruit yield, root growth, and photosynthesis in a commercial tomato cultivar under prolonged water deficit in a Mediterranean greenhouse. Integrated physiological, metabolite, and transcriptomic analyses revealed that CF mitigated drought‑induced changes, suppressing about half of water‑stress responsive genes, thereby reducing the plant’s transcriptional sensitivity to water scarcity.
MdBRC1 and MdFT2 Interaction Fine-Tunes Bud Break Regulation in Apple
Authors: Gioppato, H. A., Estevan, J., Al Bolbol, M., Soriano, A., Garighan, J., Jeong, K., Georget, C., Soto, D. G., El Khoury, S., Falavigna, V. d. S., George, S., Perales, M., Andres, F.
The study identifies the transcription factor MdBRC1 as a key inhibitor of bud growth during the ecodormancy phase in apple (Malus domestica), directly regulating dormancy‑associated genes and interacting with the flowering promoter MdFT2 to modulate bud break. Comparative transcriptomic analysis and gain‑of‑function experiments in poplar demonstrate that MdFT2 physically binds MdBRC1, attenuating its repressive activity and acting as a molecular switch for the transition to active growth.
The study profiled root transcriptomes of Arabidopsis wild type and etr1 gain-of-function (etr1-3) and loss-of-function (etr1-7) mutants under ethylene or ACC treatment, identifying 4,522 ethylene‑responsive transcripts, including 553 that depend on ETR1 activity. ETR1‑dependent genes encompassed ethylene biosynthesis enzymes (ACO2, ACO3) and transcription factors, whose expression was further examined in an ein3eil1 background, revealing that both ETR1 and EIN3/EIL1 pathways regulate parts of the network controlling root hair proliferation and lateral root formation.
Field trials of Pongamia pinnata in two subtropical Queensland sites revealed rapid biomass accumulation (13–19 kg per tree over 3–4 years) and high carbon sequestration (2.9–4.0 t C ha⁻¹) even on nutrient‑poor soils. Growth variability correlated with the maternal seed source, highlighting the importance of elite genetic material, and seedlings displayed strong drought tolerance.
The study introduced full-length SOC1 genes from maize and soybean, and a partial SOC1 gene from blueberry, into tomato plants under constitutive promoters. While VcSOC1K and ZmSOC1 accelerated flowering, all three transgenes increased fruit number per plant mainly by promoting branching, and transcriptomic profiling revealed alterations in flowering, growth, and stress‑response pathways.
Loss‑of‑function mutations in the drought‑induced genes GASA3 and AFP1 confer enhanced drought tolerance in Arabidopsis thaliana, primarily through smaller stomatal apertures and increased ABA accumulation via hydrolysis of ABA‑GE. Constitutive overexpression of these genes heightens drought sensitivity, indicating that the AFP1/GASA3 module negatively regulates stomatal closure and ABA signaling.
The study reanalyzed 1,107 public grapevine RNA‑seq datasets to build condition‑specific gene expression atlases and a whole‑genome co‑expression network associated with drought stress, and deployed these resources via a web‑based Hydric Stress Atlas App. Network topology analysis identified candidate hub genes that could serve as molecular markers or targets for gene editing to improve drought tolerance in Vitis vinifera.
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.
Priming of retrograde signaling in wheat across multiple natural environments reveal how responses to dynamic stimuli can be integrated to alter yield, yield stability and water productivity
Authors: Bowerman, A. F., Moore, M., Yadav, A., Zhang, J., Mortimer, M. D., Plskova, Z., Tee, E. E., Au, E. K., Collinge, D. P., Estavillo, G. M., Howitt, C. A., Chan, K. X., Rebetzke, G. J., Pogson, B. J.
The study generated wheat (Triticum aestivum) mutants with targeted deletions in the SAL gene family (TaSAL1 and TaSAL2) to assess the impact of chloroplast-to-nucleus retrograde signaling on field performance. Across 15 diverse Australian field trials, TaSAL2 deletions conferred 4–8% higher yields and improved water productivity by maintaining photosynthetic efficiency and dynamic stomatal control under drought, whereas TaSAL1 deletions reduced yields. These results demonstrate that locus‑specific retrograde signaling modifications can simultaneously enhance yield and stress resilience in a major crop.
The study investigates the role of the Arabidopsis transcription factor AtMYB93 in sulfur (S) signaling and root development, revealing that AtMYB93 mutants exhibit altered expression of S transport and metabolism genes and increased shoot S levels, while tomato plants overexpressing SlMYB93 show reduced shoot S. Transcriptomic profiling, elemental analysis, and promoter activity assays indicate that AtMYB93 contributes to root responses to S deprivation, though functional redundancy masks clear phenotypic effects on lateral and adventitious root formation.