Wheat plays a crucial role in global food security. However, drought stress severely restricts its growth and development, and drought during the seedling stage significantly affects its organogenesis, thereby affecting yield. To study wheat drought tolerance mechanisms at the seedling stage and to explore drought tolerance gene resources, this study focused on the drought-tolerant wheat variety Bainong 207 and performed RNA-Seq and metabolome sequencing on leaves collected at the three-leaf stage under drought stress conditions. Drought stress significantly altered the expression of 12,930 genes and 2544 metabolites in wheat seedlings. Through bioinformatics methods such as O2PLS-DA, a gene–metabolite correlation network was constructed, and key regulatory genes within this network were subsequently identified. The results identified the important gene module MEbrown and metabolite module Meta6 and finally screened 20 transcription factors that are closely related to drought response. These transcription factors were predicted to be able to combine and regulate the expression of six key genes, which together help the variety to improve drought tolerance under drought stress conditions by regulating reactive oxygen species metabolism, maintaining intracellular redox homeostasis, promoting wax biosynthesis, enhancing the osmotic stress response, and regulating abscisic acid response.
Maize ear rot, primarily caused by Fusarium verticillioides (Fusarium ear rot, FER) and Fusarium graminearum (Gibberella ear rot, GER), is a devastating disease that causes significant yield losses and mycotoxin contamination. Breeding resistant varieties is the most effective control strategy, but this requires the identification of stable genetic loci for resistance. In this study, we employed bulked segregant analysis (BSA) on two F2 mapping populations to identify quantitative trait loci (QTLs) conferring resistance to FER and GER. We identified five and eleven QTLs for FER and GER, respectively. Notably, chromosome 4 was identified as a major hotspot for resistance to both diseases, and there was a co-localization of the FER QTL (qFER4.05) and GER QTL (qGER4.05-1) within a 58.58–71.34 Mb interval on bin 4.05, suggesting a potential locus for broad-spectrum resistance. Within this overlapping region, we identified 18 high-confidence candidate genes, including genes encoding leucine-rich repeat receptor-like kinases (LRR-RLKs), remorin, cytochrome P450 monooxygenases, and wall-associated receptor kinase-like (WAKL) protein, all with established roles in plant defense. These findings advance the understanding of the genetic architecture of ear rot resistance and provide critical resources for marker-assisted breeding to develop maize hybrids with durable resistance to both FER and GER.