Department of Crop Genetics and Breeding, College of Agronomy, Gansu Agricultural University, Lanzhou 730070, China.
State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou 730070, China.
Genes (Basel). 2022 Aug 1;13(8):1379. doi: 10.3390/genes13081379.
The study was conducted with C31 and C80 genotypes of the potato ( L.), which are tolerant and susceptible to phosphite (Phi, HPO), respectively. To decipher the molecular mechanisms underlying tolerance and susceptibility to Phi in the potato, RNA sequencing was used to study the global transcriptional patterns of the two genotypes. Media were prepared with 0.25 and 0.50 mM Phi, No-phosphorus (P), and 1.25 mM (phosphate, Pi as control). The values of fragments per kilobase of exon per million mapped fragments of the samples were also subjected to a principal component analysis, grouping the biological replicates of each sample. Using stringent criteria, a minimum of 819 differential (DEGs) were detected in both C80-Phi-0.25_vs_C80-Phi-0.50 (comprising 517 upregulated and 302 downregulated) and C80-Phi-0.50_vs_C80-Phi-0.25 (comprising 302 upregulated and 517 downregulated) and a maximum of 5214 DEGs in both C31-Con_vs_C31-Phi-0.25 (comprising 1947 upregulated and 3267 downregulated) and C31-Phi-0.25_vs_C31-Con (comprising 3267 upregulated and 1947 downregulated). DEGs related to the ribosome, plant hormone signal transduction, photosynthesis, and plant-pathogen interaction performed important functions under Phi stress, as shown by the Kyoto Encyclopedia of Genes and Genomes annotation. The expressions of transcription factors increased significantly in C31 compared with C80. For example, the expressions of , , , and increased under P deficiency conditions (Phi-0.25, Phi-0.50, and No-P) relative to the control (P sufficiency) in C31. This study adds to the growing body of transcriptome data on Phi stress and provides important clues to the Phi tolerance response of the C31 genotype.
该研究以马铃薯(L.)的 C31 和 C80 基因型为对象,它们分别对亚膦酸盐(Phi,HPO)具有耐受性和敏感性。为了解马铃薯对 Phi 耐受性和敏感性的分子机制,我们使用 RNA 测序研究了这两种基因型的全转录谱。使用 0.25 和 0.50 mM Phi、无磷(P)和 1.25 mM(磷酸盐,Pi 作为对照)制备培养基。还对样本的每百万映射片段的外显子片段数的片段数进行主成分分析,将每个样本的生物学重复分组。使用严格的标准,在 C80-Phi-0.25_vs_C80-Phi-0.50(包括 517 个上调和 302 个下调)和 C80-Phi-0.50_vs_C80-Phi-0.25(包括 302 个上调和 517 个下调)中检测到至少 819 个差异表达基因(DEGs),在 C31-Con_vs_C31-Phi-0.25(包括 1947 个上调和 3267 个下调)和 C31-Phi-0.25_vs_C31-Con(包括 3267 个上调和 1947 个下调)中检测到最多 5214 个 DEGs。KEGG 注释表明,在 Phi 胁迫下,与核糖体、植物激素信号转导、光合作用和植物-病原体相互作用相关的 DEGs 发挥了重要作用。与 C80 相比,C31 中转录因子的表达显著增加。例如,在 C31 中,在 P 缺乏条件下(Phi-0.25、Phi-0.50 和 No-P),与对照(P 充足)相比,表达因子 、 、 和 显著增加。这项研究增加了关于 Phi 胁迫的转录组数据,并为 C31 基因型对 Phi 的耐受性反应提供了重要线索。