The genetic architecture of leaf vein density traits and its importance for photosynthesis in maize
Authors: Coyac-Rodriguez, J. L., Perez-Limon, S., Hernandez-Jaimes, E., Hernandez-Coronado, M., Camo-Escobar, D., Alonso-Nieves, A. L., Ortega-Estrada, M. d. J., Gomez-Capetillo, N., Sawers, R. J., Ortiz-Ramirez, C. H.
Using diverse Mexican maize varieties and a MAGIC population, the study demonstrated that leaf vein density is both variable and plastic, correlating positively with photosynthetic rates for small intermediate veins and increasing under heat in drought-adapted lines. Twelve QTLs linked to vein patterning were identified, highlighting candidate genes for intermediate vein development and shedding light on the evolution of high-efficiency C4 leaf architecture.
The study identified the poplar homolog of Arabidopsis HDG11 and generated transgenic poplar hybrids overexpressing PtaHDG11. Constitutive expression conferred markedly improved drought tolerance, as evidenced by higher leaf water content, reduced oxidative damage, up‑regulation of antioxidant genes, and greater post‑stress biomass, while also causing a glabrous phenotype. These results highlight PtaHDG11 as a promising target for breeding drought‑resilient trees.
The study assessed 17 morphological, biochemical, and salt‑stress tolerance traits in 19 maize (Zea mays) landrace accessions from northern Argentina, revealing substantial variation both within and among accessions. Redundancy analysis linked phenotypic variation to the altitude of the collection sites, underscoring the potential of these landraces as sources of diverse biochemical and stress‑related traits for breeding.
The authors performed a genome-wide analysis of 53 CCCH zinc‑finger genes in pearl millet, identified seven stress‑responsive members and demonstrated that overexpressing PgC3H50 in Arabidopsis enhances drought and salt tolerance. They showed that the ABA‑responsive transcription factor PgAREB1 directly binds the PgC3H50 promoter, activating its expression, as confirmed by yeast one‑hybrid, dual‑luciferase and EMSA assays, defining a new PgAREB1‑PgC3H50 regulatory module.
The study tests whether heavy‑metal stress contributed to maize domestication by exposing teosinte (Zea mays ssp. parviglumis) and the Palomero toluqueno landrace to sublethal copper and cadmium, then analysing genetic diversity, selection signatures, and transcriptomic responses of three chromosome‑5 heavy‑metal response genes (ZmHMA1, ZmHMA7, ZmSKUs5). Results reveal strong positive selection on these genes, heavy‑metal‑induced phenotypes resembling modern maize, and up‑regulation of Tb1, supporting a role for volcanic‑derived metal stress in early maize evolution.
The study examined how DNA methylation influences cold stress priming in Arabidopsis thaliana, revealing that primed plants exhibit distinct gene expression and methylation patterns compared to non-primed plants. DNA methylation mutants, especially met1 lacking CG methylation, showed altered cold memory and misregulation of the CBF gene cluster, indicating that methylation ensures transcriptional precision during stress recall.
A comprehensive multi‑environment trial of 437 maize testcross hybrids derived from 38 MLN‑tolerant lines and 29 testers identified additive genetic effects as the primary driver of grain yield, disease resistance, and drought tolerance. Strong general combining ability and specific combining ability patterns were uncovered, with top hybrids delivering up to 5.75 t ha⁻¹ under MLN pressure while maintaining high performance under optimum and drought conditions. The study provides a framework for selecting elite parents and exploiting both additive and non‑additive effects to develop resilient maize hybrids for sub‑Saharan Africa.
The study used paired whole‑genome bisulphite sequencing and RNA‑seq on wheat landraces to investigate how DNA methylation patterns change during drought stress, revealing antagonistic trends across cytosine contexts and a key demethylation role for ROS1a family members. Gene‑body methylation correlated positively with expression but negatively with stress‑responsive changes, while drought‑induced hyper‑methylation of specific transposable elements, especially the RLX_famc9 LTR retrotransposon, appears to modulate downstream gene regulation via siRNA precursors.
Authors: Baer, M., Zhong, Y., Yu, B., Tian, T., He, X., Gu, L., Huang, X., Gallina, E., Metzen, I. E., Bucher, M., Song, R., Gutjahr, C., SU, Z., Moya, Y., von Wiren, N., Zhang, L., Yuan, L., Shi, Y., Wang, S., Qi, W., Baer, M., Zhao, Z., Li, C., Li, X., Hochholdinger, F., Yu, P.
The study uncovers how arbuscular mycorrhizal (AM) fungi induce lateral root formation in maize by activating ethylene‑responsive transcription factors (ERFs) that regulate pericycle cell division and reshape flavonoid metabolism, lowering inhibitory flavonols. It also shows that the rhizobacterium Massilia collaborates with AM fungi, degrading flavonoids and supplying auxin, thereby creating an integrated ethylene‑flavonoid‑microbe signaling network that can be harnessed to improve nutrient uptake and crop sustainability.
The mRNA covalent modification dihydrouridine regulates transcript turnover and photosynthetic capacity during plant abiotic stress
Authors: Yu, L., Melandri, G., Dittrich, A. C., Calleja, S., Rozzi, B., Ganguly, D. R., Palos, K., Srinivasan, A., Brewer, E. K., Fischer, H., Obata, T., Elgawad, H. A., Beemster, G. T. S., Henderson, R., Garcia, C. D., Zhang, X., Stern, D., Eveland, A., Schroeder, S. J., Skirycz, A., Lyons, E., Arnold, E. A., Gregory, B. D., Nelson, A. D. L., Pauli, D.
The study integrates multi-omics data from six Sorghum bicolor accessions under field drought to link RNA covalent modifications (RCMs) with photosynthetic performance, identifying the enzyme SbDUS2 that produces dihydrouridine (DHU) on transcripts. Loss‑of‑function dus2 mutants in Arabidopsis thaliana reveal that DHU deficiency leads to hyperstability of photosynthesis‑related mRNAs, impairing germination, development, and stress‑induced CO2 assimilation. The authors propose DHU as a post‑transcriptional mark that promotes rapid mRNA turnover during abiotic stress, enhancing plant resilience.