ABSTRACT
Foxtail millet (Setaria italica) is a monotypic species widely planted in China. However, residual atrazine, a commonly used maize herbicide, in soil, is a major abiotic stress to millet. Here, we investigated atrazine tolerance in millet based on the field experiments, then obtained an atrazine-resistant variety (Gongai2, GA2) and an atrazine-sensitive variety (Longgu31, LG31). To examine the effects of atrazine on genes and metabolites in millet plants, we compared the transcriptomic and metabolomic profiles between GA2 and LG31 seedling leaves. The results showed that 2,208 differentially expressed genes (DEGs; 501 upregulated, 1,707 downregulated) and 192 differentially expressed metabolites (DEMs; 82 upregulated, 110 downregulate) were identified in atrazine-treated GA2, while in atrazine-treated LG31, 1,773 DEGs (761 upregulated, 1,012 downregulated) and 215 DEMs (95 upregulated, 120 downregulated) were identified. The bioinformatics analysis of DEGs and DEMs showed that many biosynthetic metabolism pathways were significantly enriched in GA2 and LG31, such as glutathione metabolism (oxiglutatione, γ-glutamylcysteine; GSTU6, GSTU1, GSTF1), amino acid biosynthesis (L-cysteine, N-acetyl-L-glutamic acid; ArgB, GS, hisC, POX1), and phenylpropanoid biosynthesis [trans-5-o-(4-coumaroyl)shikimate; HST, C3'H]. Meanwhile, the co-expression analysis indicated that GA2 plants had enhanced atrazine tolerance owing to improved glutathione metabolism and proline biosynthesis, and the enrichment of scopoletin may help LG31 plants resist atrazine stress. Herein, we screened an atrazine-resistant millet variety and generated valuable information that may deepen our understanding of the complex molecular mechanism underlying the response to atrazine stress in millet.
ABSTRACT
Plant fatty acid desaturases (FADs) catalyze the desaturation of fatty acids in various forms and play important roles in regulating fatty acid composition and maintaining membrane fluidity under temperature stress. A total of 30 FADs were identified from a maize genome, including 13 soluble and 17 membrane-bound FADs, which were further classified into two and five sub-groups, respectively, via phylogenetic analysis. Although there is no evolutionary relationship between the soluble and the membrane-bound FADs, they all harbor a highly conserved FA_desaturase domain, and the types and the distributions of conserved motifs are similar within each sub-group. The transcriptome analysis revealed that genes encoding FADs exhibited different expression profiles under cold and heat stresses. The expression of ZmFAD2.1&2.2, ZmFAD7, and ZmSLD1&3 were significantly up-regulated under cold stress; moreover, the expression of ZmFAD2.1&2.3 and ZmSLD1&3 were obviously down-regulated under heat stress. The co-expression analysis demonstrated close correlation among the transcription factors and the significant responsive FAD genes under cold or heat stress. This study helps to understand the roles of plant FADs in temperature stress responses.