Juan Lu

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.

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.

Wheat is an important global food crop. The peduncle significantly impacts the plant’s height, architecture, and yield, and understanding its genetic mechanisms is crucial not only for improving wheat’s architecture but also for enhancing its yield. In this study, we identified an elongated uppermost internode (eui) mutant in the EMS-induced progeny of Jinmai 90 (JM90). We conducted phenotypic identification, genetic analysis, and cytological observation combined with transcriptome and targeted hormone metabolism analysis and compared the differences between the eui mutant and the wild-type (WT). The results indicated that an incompletely dominant gene mutation caused the eui mutant to display significant elongation of the peduncle and an increase in the plant height. This was attributed to the considerable elongation of parenchyma cells, while no significant differences were noted in other internodes. These traits were accompanied by an increase in the spikelets per spike and grains per spike. Subsequently, transcriptome and targeted hormone metabolome sequencing were performed and identified 15,969 differentially expressed genes (DEGs) and 27 hormone-related differentially accumulated metabolites (DAMs). KEGG enrichment analysis indicated that the DEGs in MS1_VS_WS1 were significantly enriched in two pathways: those related to tryptophan metabolism and diterpenoid biosynthesis. Analysis indicated that the peduncle elongation caused by the eui mutant is primarily regulated by auxin. This study offers a foundation for the exploration and cloning of genes associated with the peduncle, establishing a theoretical basis for understanding the molecular mechanisms behind wheat peduncle elongation and for developing ideal plant types and breeding high-yield varieties.

Nitrogen crucially impacts foxtail millet (Setaria italica) growth and development. Uncovering low nitrogen (LN) tolerance genes and mechanisms is vital for breeding high nitrogen use efficiency varieties. In this study, the LN tolerance of 50 foxtail millet genotypes was assessed through field trials and seedling hydroponic experiments. Subsequently, transcriptome analysis was performed on one highly sensitive genotype, named Maotigu, and on one highly tolerant genotype, named Dahuanggu, under LN (0.1 mmol/L) and control (5 mmol/L) conditions in seedling hydroponic experiments. Compared to the control treatment, 823 differentially expressed genes (DEGs) (350 upregulated, 473 downregulated) were identified in the roots of Dahuanggu, while 2427 DEGs (1703 upregulated, 724 downregulated) were detected in Maotigu under LN treatment. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed that a total of 3134 DEGs were associated with pathways including plant–pathogen interaction, amino sugar and nucleotide sugar metabolism, nitrogen metabolism, and others. A total of 116 DEGs were commonly identified between Dahuanggu and Maotigu, involving pathways like plant–pathogen interaction, galactose metabolism, and flavone and flavonol biosynthesis. The 28 of 116 DEGs showed opposite expression patterns between Dahuanggu and Maotigu; the expression of 18 genes was further validated using qRT-PCR. These offer valuable insights into the molecular mechanisms underlying LN stress responses in foxtail millet.

Premature leaf senescence has a profound influence on crop yield and quality. Here, a stable premature senescence mutant (GSm) was obtained from the common wheat (Triticum aestivum L.) cultivar Chang 6878 by mutagenesis with ethyl methanesulfonate. The differences between the GSm mutant and its wild-type (WT) were analyzed in terms of yield characteristics, photosynthetic fluorescence indices, and senescence-related physiological parameters. RNA sequencing was used to reveal gene expression differences between GSm and WT. The results showed that the yield of GSm was considerably lower than that of WT. The net photosynthetic rate, transpiration rate, maximum quantum yield, non-photochemical quenching coefficient, photosynthetic electron transport rate, soluble protein, peroxidase activity, and catalase activity all remarkably decreased in flag leaves of GSm, whereas malondialdehyde content distinctively increased compared with those of WT. The analysis of differentially expressed genes indicated blockade of chlorophyll and carotenoid biosynthesis, accelerated degradation of chlorophyll, and diminished photosynthetic capacity in mutant leaves; brassinolide might facilitate chlorophyll breakdown and consequently accelerate leaf senescence. NAC genes positively regulated the senescence process. Compared with NAC genes, expression of WRKY and MYB genes was induced earlier in the mutant possibly due to increased levels of reactive oxygen species and plant hormones (e.g., brassinolide, salicylic acid, and jasmonic acid), thereby accelerating leaf senescence. Furthermore, the antioxidant system played a role in minimizing oxidative damage in the mutant. These results provides novel insight into the molecular mechanisms of premature leaf senescence in crops.