Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida, USA.
Department of Biology, Miami University, Oxford, Ohio, USA.
Plant Genome. 2024 Sep;17(3):e20487. doi: 10.1002/tpg2.20487. Epub 2024 Jul 12.
Phytophthora root rot, caused by oomycete pathogens in the Phytophthora genus, poses a significant threat to soybean productivity. While resistance mechanisms against Phytophthora sojae have been extensively studied in soybean, the molecular basis underlying immune responses to Phytophthora sansomeana remains unclear. In this study, we investigated transcriptomic and epigenetic responses of two resistant (Colfax and NE2701) and two susceptible (Williams 82 and Senaki) soybean lines at four time points (2, 4, 8, and 16 h post inoculation [hpi]) after P. sansomeana inoculation. Comparative transcriptomic analyses revealed a greater number of differentially expressed genes (DEGs) upon pathogen inoculation in resistant lines, particularly at 8 and 16 hpi. These DEGs were predominantly associated with defense response, ethylene, and reactive oxygen species-mediated defense pathways. Moreover, DE transposons were predominantly upregulated after inoculation, and more of them were enriched near genes in Colfax than other soybean lines. Notably, we identified a long non-coding RNA (lncRNA) within the mapped region of the resistance gene that exhibited exclusive upregulation in the resistant lines after inoculation, potentially regulating two flanking LURP-one-related genes. Furthermore, DNA methylation analysis revealed increased CHH (where H = A, T, or C) methylation levels in lncRNAs after inoculation, with delayed responses in Colfax compared to Williams 82. Overall, our results provide comprehensive insights into soybean responses to P. sansomeana, highlighting potential roles of lncRNAs and epigenetic regulation in plant defense.
疫霉根腐病由疫霉属卵菌引起,对大豆生产力构成重大威胁。尽管已对大豆抗大豆疫霉(Phytophthora sojae)的机制进行了广泛研究,但对大豆抗大豆南方疫霉(Phytophthora sansomeana)免疫反应的分子基础仍不清楚。在这项研究中,我们在接种后 2、4、8 和 16 小时(hpi)的四个时间点研究了两个抗性(Colfax 和 NE2701)和两个敏感(Williams 82 和 Senaki)大豆品系对 P. sansomeana 接种的转录组和表观遗传反应。比较转录组分析表明,抗性系中接种病原体后差异表达基因(DEGs)的数量更多,特别是在 8 和 16 hpi。这些 DEGs 主要与防御反应、乙烯和活性氧介导的防御途径有关。此外,接种后 DE 转座子主要上调,Colfax 中附近基因的转座子比其他大豆品系更多。值得注意的是,我们在抗性基因的映射区域内鉴定出一个长非编码 RNA(lncRNA),该基因在接种后仅在抗性系中上调,可能调节两个侧翼的 LURP-one 相关基因。此外,DNA 甲基化分析表明,lncRNA 中的 CHH(其中 H=A、T 或 C)甲基化水平在接种后增加,Colfax 的反应比 Williams 82 延迟。总体而言,我们的研究结果提供了大豆对 P. sansomeana 反应的全面见解,强调了 lncRNA 和表观遗传调控在植物防御中的潜在作用。