Department of Biology, Miami University, Oxford, OH 45056, USA.
Plant Molecular and Cellular Biology Graduate Program, University of Florida, Gainesville, FL 32611, USA.
G3 (Bethesda). 2024 Oct 7;14(10). doi: 10.1093/g3journal/jkae191.
Phytophthora sansomeana is an emerging oomycete pathogen causing root rot in many agricultural species including soybean. However, as of now, only one potential resistance gene has been identified in soybean, and our understanding of how genetic and epigenetic regulation in soybean contributes to responses against this pathogen remains largely unknown. In this study, we performed whole genome bisulfite sequencing (WGBS) on two soybean lines, Colfax (resistant) and Williams 82 (susceptible), in response to P. sansomeana at two time points: 4 and 16 hours post-inoculation to compare their methylation changes. Our findings revealed that there were no significant changes in genome-wide CG, CHG (H = A, T, or C), and CHH methylation. However, we observed local methylation changes, specially an increase in CHH methylation around genes and transposable elements (TEs) after inoculation, which occurred earlier in the susceptible line and later in the resistant line. After inoculation, we identified differentially methylated regions (DMRs) in both Colfax and Williams 82, with a predominant presence in TEs. Notably, our data also indicated that more TEs exhibited changes in their methylomes in the susceptible line compared to the resistant line. Furthermore, we discovered 837 DMRs within or flanking 772 differentially expressed genes (DEGs) in Colfax and 166 DMRs within or flanking 138 DEGs in Williams 82. These DEGs had diverse functions, with Colfax primarily showing involvement in metabolic process, defense response, plant and pathogen interaction, anion and nucleotide binding, and catalytic activity, while Williams 82 exhibited a significant association with photosynthesis. These findings suggest distinct molecular responses to P. sansomeana infection in the resistant and susceptible soybean lines.
桑氏腐霉是一种新兴的卵菌病原体,可导致包括大豆在内的许多农业物种的根腐病。然而,到目前为止,大豆中仅鉴定出一个潜在的抗性基因,我们对大豆中遗传和表观遗传调控如何有助于对该病原体的反应的理解在很大程度上仍然未知。在这项研究中,我们对 Colfax(抗性)和 Williams 82(敏感)两个大豆品系在接种 P. sansomeana 后两个时间点(接种后 4 小时和 16 小时)进行了全基因组亚硫酸氢盐测序(WGBS),以比较它们的甲基化变化。我们的研究结果表明,全基因组 CG、CHG(H=A、T 或 C)和 CHH 甲基化没有明显变化。然而,我们观察到局部甲基化变化,特别是在接种后基因和转座元件(TEs)周围的 CHH 甲基化增加,这种变化在敏感系中更早发生,在抗性系中更晚发生。接种后,我们在 Colfax 和 Williams 82 中都鉴定出差异甲基化区域(DMR),主要存在于 TEs 中。值得注意的是,我们的数据还表明,与抗性系相比,更多的 TEs 在其甲基组中发生了变化。此外,我们在 Colfax 中发现了 837 个 DMRs 位于或侧翼于 772 个差异表达基因(DEGs)中,在 Williams 82 中发现了 166 个 DMRs 位于或侧翼于 138 个 DEGs 中。这些 DEGs 具有多种功能,Colfax 主要参与代谢过程、防御反应、植物与病原体相互作用、阴离子和核苷酸结合以及催化活性,而 Williams 82 与光合作用显著相关。这些发现表明在抗性和敏感大豆品系中对 P. sansomeana 感染有不同的分子反应。