Soil salinization is the main abiotic stressor faced by crops. An improved understanding of the transcriptional response to salt stress in roots, the organ directly exposed to a high salinity environment, can inform breeding strategies to enhance tolerance and increase crop yield. Here, RNA-sequencing was performed on the roots of salt-tolerant wheat breeding line CH7034 at 0, 1, 6, 24, and 48 h after NaCl treatment. Based on transcriptome data, a weighted gene co-expression network analysis (WGCNA) was constructed, and five gene co-expression modules were obtained, of which the blue module was correlated with the time course of salt stress at 1 and 48 h. Two GO terms containing 249 differentially expressed genes (DEGs) related to osmotic stress response and salt-stress response were enriched in the blue module. These DEGs were subsequently used for association analysis with a set of wheat germplasm resources, and the results showed that four genes, namely a Walls Are Thin 1-related gene (TaWAT), an aquaporin gene (TaAQP), a glutathione S-transfer gene (TaGST), and a zinc finger gene (TaZFP), were associated with the root salt-tolerance phenotype. Using the four candidate genes as hub genes, a co-expression network was constructed with another 20 DEGs with edge weights greater than 0.6. The network showed that TaWAT and TaAQP were mainly co-expressed with fifteen interacting DEGs 1 h after salt treatment, while TaGST and TaZFP were mainly co-expressed with five interacting DEGs 48 h after salt treatment. This study provides key modules and candidate genes for understanding the salt-stress response mechanism in wheat roots.

Soil salinization is a major abiotic stressor that significantly reduces wheat yield. Identifying novel salt-tolerance genes and integrating them into wheat breeding programs can enhance wheat productivity in saline soils. Ethylene response factor (ERF) plays an important role in plant response to salt stress, and thus far, four wheat ERF genes have been identified to be involved in salt stress response. To systematically identify salt tolerance-related ERF genes in wheat, in this study, 213 ERF sequences were isolated from the whole genome of common wheat and classified into 54 members based on subgenome homology, named TaERF1 to TaERF54. Transcriptome sequencing results showed different expression patterns of TaERF members in leaves after 1, 6, 24, and 48 h of NaCl treatment. Based on association analysis, nine TaERF genes were correlated with the leaf salt injury index. Among them, five SNPs of TaERF16-B formed two haplotypes: Hap1 and Hap2. RT-qPCR results showed that the expression level of TaERF16-B was significantly higher in Hap2-typed germplasms than that in Hap1-typed germplasms after 1 and 6 h of NaCl treatment. A Kompetitive Allele-Specific PCR marker K52 was developed for genotyping TaERF16-B haplotypes, which further confirmed the significant correlation between TaERF16-B and salt tolerance-related phenotypes in mapping population and wheat germplasms. This study provides new genes and molecular markers for improving salt tolerance in wheat.

Stem lodging critically limits wheat yield stability, with its resistance heavily influenced by internode mechanical strength, a trait whose genetic architecture remains poorly resolved. This study aimed to dissect the genetic basis of stem strength in the first three basal internodes of wheat. Using a panel of 224 cultivars, we measured internode strength across two environments and performed a genome-wide association study with 269,708 SNPs, employing the FarmCPU model. Three stable quantitative trait loci (QTL) associated with internode stem strength were identified: QI1SS.sau.5A, QI2SS.sau.2D, and QI2SS.sau.6B across a diverse wheat panel, with allele-dependent effects observed among accessions. Among them, QI2SS.sau.2D consistently enhanced stem strength across all three internodes, explaining up to 10.8% of phenotypic variance, without adverse effects on plant height or thousand-grain weight. In contrast, the other two QTL were associated with trade-offs, such as reduced plant height or grain weight. These results reveal a polygenic and partially internode-shared genetic regulation of stem strength. The locus QI2SS.sau.2D is highlighted as a particularly promising, penalty-free target for marker-assisted selection to improve lodging resistance while maintaining agronomic performance, including plant height and thousand-grain weight.