Cryptochromes (CRYs), as essential blue-light photoreceptors, play pivotal roles in modulating plant growth, development, and stress responses. Although CRY-mediated light signaling has been extensively studied in model species, their functions remain limited in wheat. In this work, a comprehensive analysis of the TaCRY gene family was performed in wheat, identifying 12 TaCRY members localized to distinct chromosomes 2, 6, and 7. TaCRYs contain the conserved PHR and CCT domains and diverse gene structures. Collinearity relationships indicated their dynamic evolution patterns during polyploidization. Cis-acting elements of TaCRY members associated with light responsiveness, phytohormone signaling, and abiotic stress were also identified. Transcriptome analysis revealed that the differential expression patterns of TaCRY members under seed vigor process. This study expands our understanding of TaCRY diversity and provides valuable molecular information for marker-assisted selection in wheat improvement.

Background: Ammonium nitrogen (NH₄⁺) serves as a vital nitrogen source, playing pivotal regulatory roles in plant growth, development, and high-yield formation. Ammonium transporters (AMTs), encoded by the AMT gene family, are central to NH₄⁺ transport. However, the functional roles of AMT genes in wheat remain poorly understood. Methods: A comprehensive genome-wide analysis of the TaAMT gene family numbers was conducted, encompassing investigations into gene structure, protein motif composition, gene duplication events, collinearity relationships, and cis-acting regulatory elements. Furthermore, the expression patterns of distinct TaAMT members were examined under varying ammonium supply conditions and pathogen stress. Results: In this study, a total of 21 TaAMT members were identified. Additionally, all TaAMT proteins were localized to the plasma membrane. Phylogenetic analysis clustered these genes into four distinct subgroups. Comparative analyses of gene structure and conserved motifs revealed conserved domain composition and motif organization within each subgroup. Interspecific synteny analysis highlighted evolutionary conservation across species. Promoter region analysis identified multiple cis-regulatory elements associated with hormone signaling, light responsiveness, and abiotic stress adaptation. Expression profiling demonstrated that TaAMT members exhibit both tissue-specific and constitutive expression patterns across developmental stages. RT-qPCR further revealed that the expression of TaAMT members responds to varying concentrations of ammonium nitrogen supply, as well as infection stresses caused by stripe rust and powdery mildew. Conclusions: Collectively, this study uncovered the functional diversity of TaAMT members, offering novel molecular targets and theoretical foundations for breeding wheat varieties with enhanced nitrogen use efficiency and disease resistance.

Background: Ammonium nitrogen (NH₄⁺) serves as a vital nitrogen source, playing pivotal regulatory roles in plant growth, development, and high-yield formation. Ammonium transporters (AMTs), encoded by the AMT gene family, are central to NH4+ transport. However, the functional roles of AMT genes in wheat remain poorly understood.Methods: In this study, a total of 21 TaAMT members were identified. A comprehensive genome-wide analysis was conducted, encompassing investigations into gene structure, protein motif composition, gene duplication events, collinearity relationships, and cis-acting regulatory elements. Furthermore, the expression patterns of distinct TaAMT members were examined under varying ammonium supply conditions and pathogen stress. Results: All TaAMT proteins exhibited hydrophobic characteristics and localized to the plasma membrane. Phylogenetic analysis clustered these genes into four distinct subgroups. Comparative analyses of gene structure and conserved motifs revealed conserved domain composition and motif organization within each subgroup. Interspecific synteny analysis highlighted evolutionary conservation across species. Promoter region analysis identified multiple cis-regulatory elements associated with hormone signaling, light responsiveness, and abiotic stress adaptation. Expression profiling demonstrated that TaAMT members exhibit both tissue-specific and constitutive expression patterns across developmental stages. RT-qPCR further revealed that the expression of TaAMT members responds to varying concentrations of ammonium nitrogen supply, as well as infection stresses caused by stripe rust and powdery mildew. Conclusions: Collectively, this study provides the useful molecular information into the roles of TaAMT members in nitrogen use efficiency and disease resistance, offering valuable genetic resources for wheat breeding programs aimed at enhancing agronomic traits.

The ABCB subfamily, a subset transporter of the ATP-binding cassette (ABC) superfamily, is vital for various plant life processes, especially in the transport of polar auxin and brassinosteroids. Although ABCB transporters have been characterized in diverse plant species, their specific functions in wheat remain largely unexplored. In this study, we identified 99 TaABCB members in wheat and categorized them into four groups based on their conserved domains and phylogenetic relationships. These members were found to be unevenly distributed across all 21 wheat chromosomes. We conducted a comprehensive genome-wide analysis encompassing gene structure, protein motifs, gene duplication events, collinearity, and cis-acting elements. Transcriptome analysis revealed that different TaABCB members displayed distinct expression patterns under phosphate starvation stress. Notably, we discovered that TaABCB7 might play a role in regulating wheat’s phosphate starvation. Crucially, we pinpointed an elite haplotype, H001, of the candidate gene TaABCB7, which has been progressively selected and employed in wheat breeding improvement programs. Overall, this study enhances our comprehensive understanding of TaABCB members and offers a potential gene resource for molecular marker-assisted selection breeding in wheat.

INDETERMINATE DOMAIN (IDD) transcription factors are plant-specific regulators essential for plant development and stress adaptation. As a globally important staple crop, common wheat (Triticum aestivum L.) is frequently threatened by fungal diseases such as powdery mildew and stripe rust. To date, however, the IDD gene family in wheat has not been systematically characterized, and its roles in biotic stress responses remain unclear. In this study, we performed genome-wide identification and a comprehensive analysis of the TaIDD gene family. A total of 41 TaIDD genes were identified, which were unevenly distributed across 15 chromosomes and divided into four phylogenetic groups. Synteny and selective pressure analyses demonstrated that segmental duplication was the main driver of family expansion and that TaIDD genes underwent strong purifying selection during evolution. Cis-acting element analysis revealed abundant hormone- and stress-related elements in their promoter regions. Transcriptome and RT-qPCR analyses indicated that TaIDD genes exhibited distinct expression patterns under abiotic and biotic stress. Notably, TaIDD13, TaIDD19, TaIDD27, TaIDD37, TaIDD39, and TaIDD41 were significantly induced by multiple fungal pathogens, suggesting their potential involvement in stress-responsive pathways that may be related to disease resistance. Subcellular localization analysis further confirmed that TaIDD39 was exclusively localized in the nucleus, consistent with its function as a transcriptional regulator. Our findings provide insights into the evolutionary characteristics and stress-response mechanisms of TaIDD genes and highlight TaIDD39 and other potential candidates that may serve as valuable resources for wheat molecular breeding to enhance broad-spectrum disease resistance and stress tolerance.

Carotenoid content is a key trait that defines the unique characteristics of foxtail millet varieties. Varieties with different levels of carotenoids often show distinct genetic features and nutritional profiles. However, the genetic basis of carotenoid content in foxtail millet remains mostly unknown. In this study, we explored the genetic basis of carotenoid content using a recombinant inbred line (RIL) population of 305 lines derived from two parental accessions, JG21 (high-carotenoid, 16.75 mg·kg⁻¹) and JG25 (low-carotenoid, 0.93 mg·kg⁻¹). The results showed that the RIL population exhibited continuous phenotypic variation and significant transgressive segregation for carotenoid components (lutein, zeaxanthin, β-cryptoxanthin) and kernel color (measured by b* value), with zeaxanthin reaching 8.47 mg·kg⁻¹, significantly surpassing the higher parent (3.44 mg·kg⁻¹) in 24DY. To ensure that enhancing this nutritional trait does not compromise grain yield, we analyzed its relationship with key agronomic traits, testing for pleiotropic trade-offs. Notably, carotenoid content showed no significant correlation with any of the 8 key agronomic traits (r ranged from −0.11 to 0.08, all p > 0.05), suggesting no apparent trade-off, although fine-mapping is needed to separate pleiotropy from tight linkage for concurrent improvement. Genetic modeling analysis revealed that carotenoid content is stably controlled by three major-gene pairs plus polygenes (MX3-AI-A model), with major-gene heritability of 96.65% and polygene heritability of 3.35%. Based on this framework, three elite RILs with >23% higher carotenoid and superior agronomic performance were identified and advanced to marker-assisted backcrossing. These results provide a clear genetic framework and immediate breeding resources for marker-assisted selection, enabling the development of high-yielding, carotenoid-enriched foxtail millet varieties without compromising agronomic value.