The study presents an optimized Agrobacterium-mediated transformation protocol for bread wheat that incorporates a GRF4‑GIF1 fusion to enhance regeneration and achieve genotype‑independent transformation across multiple cultivars. The approach consistently improves transformation efficiency while limiting pleiotropic effects, offering a versatile platform for functional genomics and gene editing in wheat.
DECREASE IN DNA METHYLATION 1-mediated epigenetic regulation maintains gene expression balance required for heterosis in Arabidopsis thaliana
Authors: Matsuo, K., Wu, R., Yonechi, H., Murakami, T., Takahashi, S., Kamio, A., Akter, M. A., Kamiya, Y., Nishimura, K., Matsuura, T., Tonosaki, K., Shimizu, M., Ikeda, Y., Kobayashi, H., Seki, M., Dennis, E. S., Fujimoto, R.
The study demonstrates that the chromatin remodeler DDM1 is essential for biomass heterosis in Arabidopsis thaliana hybrids, as loss of DDM1 function leads to reduced rosette growth and extensive genotype‑specific transcriptomic and DNA methylation changes. Whole‑genome bisulfite sequencing revealed widespread hypomethylation in ddm1 mutants, while salicylic acid levels were found unrelated to heterosis, indicating that epigenetic divergence, rather than SA signaling, underpins hybrid vigor.
The study characterizes a paralogous desaturase in the moss Physcomitrium patens, demonstrating that these enzymes (renamed VFADs) influence both sphingolipid and glycerolipid metabolism by desaturating very‑long‑chain fatty acyl‑CoA substrates. Heterologous expression in Saccharomyces cerevisiae and mutant analysis confirm activity on VLCFAs incorporated into sphingolipids, triacylglycerols, and acyl‑CoAs, suggesting a broader substrate scope than previously thought.
The authors introduced a polycistronic tRNA‑gRNA array for CRISPR/Cas9 editing in Physcomitrium patens that doubled the frequency of large, targeted deletions compared with conventional single‑gRNA constructs. Using dual‑gRNA targeting, they achieved simultaneous deletion of two to four genes (katanin and TPX2 families) in a single transformation, reaching up to 42% efficiency per gene, though efficiency depended on gRNA pair design.
The study applied a progressive, sublethal drought treatment to Arabidopsis thaliana, collecting time‑resolved phenotypic and transcriptomic data. Machine‑learning analysis revealed distinct drought stages driven by multiple overlapping transcriptional programs that intersect with plant aging, and identified high‑explanatory‑power transcripts as biomarkers rather than causal agents.
Salt stress strongly suppresses root growth in Festuca rubra while sparing shoot development. Transcriptome profiling identified over 68,000 differentially expressed genes, with up‑regulated genes enriched in methionine, melatonin, and suberin biosynthesis and down‑regulated genes involved in gibberellin, ABA, and sugar signaling, indicating extensive hormonal and metabolic reprogramming. Paradoxical regulation of gibberellin and ethylene pathways suggests a finely tuned balance between growth and stress responses.
The study examined how single and repeated mechanical disturbances (whole‑pot drops) affect leaf folding in Mimosa pudica, using chlorophyll fluorescence to track photosystem II efficiency and transcriptome profiling to identify responsive genes. A single drop mainly up‑regulated flavonoid biosynthesis genes, whereas multiple drops triggered broader biotic and abiotic stress pathways, indicating a shift in the plant’s gene regulatory network under repeated stress.
The study identifies the Arabinogalactan protein SLEEPING BEAUTY (SB) from the bryophyte Physcomitrium patens as a highly glycosylated, intrinsically disordered protein that rigidifies the cell wall and facilitates orderly cellulose microfibril deposition, with loss of function leading to softened walls. Critical proline‑linked glycosylation sites required for SB’s disordered conformation, osmotic stress‑induced endocytosis, and tonoplast trafficking were pinpointed using pharmacological inhibition and mutagenesis, and the wall‑rigidifying role of SB was shown to be conserved in Arabidopsis.
Enhancement of Arabidopsis growth by Enterobacter sp. SA187 under elevated CO2 is dependent on ethylene signalling activation and primary metabolism reprogramming
Authors: Ilyas, A., Mauve, C., Pateyron, S., Paysant-Le Roux, C., Bigeard, J., Hodges, M., de Zelicourt, A.
The study shows that inoculating Arabidopsis thaliana with the plant‑growth‑promoting bacterium Enterobacter sp. SA187 markedly boosts root and shoot biomass under elevated CO₂, accompanied by altered nitrogen and carbon content and reshaped phytohormone signaling. Transcriptomic and metabolomic analyses reveal activation of salicylic acid, jasmonic acid, and ethylene pathways and enhanced primary metabolism, while the ethylene‑insensitive ein2‑1 mutant demonstrates that the growth benefits are ethylene‑dependent.
The study examined soybean (Glycine max) responses to simultaneous drought and Asian soybean rust infection using combined transcriptomic and metabolomic analyses. Weighted Gene Co-expression Network Analysis identified stress-specific gene modules linked to metabolites, while Copula Graphical Models uncovered sparse, condition‑specific networks, revealing distinct molecular signatures for each stress without overlapping genes or metabolites. The integrative approach underscores a hierarchical, modular defense architecture and suggests targets for breeding multi‑stress resilient soybeans.