Biotechnology Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Beijing 100081, China.
National Key Facility for Crop Gene Resources and Genetic Improvement (NFCRI), Institute of Crop Sciences, Chinese Academy of Agriculture Sciences (CAAS), Beijing 100081, China.
Int J Mol Sci. 2023 Feb 20;24(4):4229. doi: 10.3390/ijms24044229.
Nucleocytoplasmic transport receptors play key roles in the nuclear translocation of disease resistance proteins, but the associated mechanisms remain unclear. The gene encodes an importin β-like protein. A transgenic Arabidopsis line overexpressing (OESAD2/Col-0) showed obvious resistance to pv. tomato DC3000 ( DC3000) compared to the wild type (Col-0), but the knockout mutant was susceptible. Transcriptomic analysis was then performed on Col-0, OESAD2/Col-0, and leaves at 0, 1, 2, and 3 days post-inoculation with DC3000. A total of 1825 differentially expressed genes (DEGs) were identified as putative biotic stress defense genes regulated by SAD2, 45 of which overlapped between the knockout and overexpression datasets. Gene Ontology (GO) analysis indicated that the DEGs were broadly involved in single-organism cellular metabolic processes and in response to stimulatory stress. Kyoto Encyclopedia of Genes and Genomes (KEGG) biochemical pathway analysis revealed that many of the DEGs were associated with the biosynthesis of flavonoids and other specialized metabolites. Transcription factor analysis showed that a large number of ERF/AP2, MYB, and bHLH transcription factors were involved in SAD2-mediated plant disease resistance. These results provide a basis for future exploration of the molecular mechanisms associated with SAD2-mediated disease resistance and establish a set of key candidate disease resistance genes.
核质转运受体在疾病抗性蛋白的核转运中发挥关键作用,但相关机制仍不清楚。该基因编码一种输入蛋白β样蛋白。与野生型(Col-0)相比,过表达(OESAD2/Col-0)的拟南芥转基因系对 pv.番茄 DC3000(DC3000)表现出明显的抗性,但敲除突变体则易感。然后对 Col-0、OESAD2/Col-0 和用 pv.番茄 DC3000(DC3000)接种 0、1、2 和 3 天后的叶片进行转录组分析。鉴定出 1825 个差异表达基因(DEGs),这些基因被认为是受 SAD2 调控的假定生物胁迫防御基因,其中 45 个在敲除和过表达数据集之间重叠。GO 分析表明,这些 DEGs 广泛参与了单个生物体的细胞代谢过程和对刺激应激的反应。KEGG 生化途径分析表明,许多 DEGs 与类黄酮和其他特殊代谢物的生物合成有关。转录因子分析表明,大量的 ERF/AP2、MYB 和 bHLH 转录因子参与了 SAD2 介导的植物疾病抗性。这些结果为未来探索与 SAD2 介导的疾病抗性相关的分子机制提供了基础,并建立了一组关键的候选疾病抗性基因。