Shim Sangrea, Kang In-Jeong, You Hee Jin, Kim Hangil, Lee Sungwoo
Department of Forest Resources, College of Forest and Environmental Sciences, Kangwon National University, Chuncheon 24341, Korea.
Division of Crop Cultivation and Environment Research, National Institute of Crop Science, Suwon 16613, Korea.
Plant Pathol J. 2024 Dec;40(6):641-655. doi: 10.5423/PPJ.OA.09.2024.0154. Epub 2024 Dec 1.
Phytophthora root and stem rot, caused by Phytophthora sojae, considerably reduces soybean yield worldwide. Our previous study identified two genomic regions on chromosome 18 (2.1-2.6 and 53.1-53.3 Mbp) that confer resistance to the P. sojae isolate 2457, through linkage analysis using progenies derived from the Daepung × Socheong2 population. These two regions contained 51 and 19 annotated genes, respectively. However, the specific gene responsible for resistance to P. sojae isolate 2457 has yet to be identified. In this study, we performed a comparative transcriptomic analysis of Socheong2 and Daepung, two Korean soybean varieties identified as resistant and susceptible to P. sojae isolate 2457, respectively. RNA sequencing was conducted on tissue samples collected at 0, 6, and 12 hours after inoculation (HAI), and significant differences in the expression of defense-related genes were observed across time points and between the two cultivars. Genes associated with the jasmonic acid, salicylic acid, ethylene, and systemic acquired resistance pathways were upregulated in both cultivars at 6 and 12 HAI compared to 0 HAI, with these biological processes were more strongly upregulated in Socheong2 compared to Daepung at 6 and 12 HAI. A comparison of differentially expressed genes (DEGs) and candidate genes within the previously identified QTL regions revealed an ortholog of the HS1 PRO-1 2 gene from Arabidopsis thaliana among the upregulated DEGs in Socheong2, particularly at 12 HAI compared to 0 HAI. This study will aid in targeted breeding efforts to develop soybean varieties with improved resistance to P. sojae.
由大豆疫霉引起的疫霉根腐和茎腐病在全球范围内大幅降低了大豆产量。我们之前的研究通过使用大浦×绥农2号群体衍生的后代进行连锁分析,在18号染色体上确定了两个基因组区域(2.1 - 2.6和53.1 - 53.3兆碱基对),它们赋予了对大豆疫霉分离株2457的抗性。这两个区域分别包含51个和19个注释基因。然而,尚未确定对大豆疫霉分离株2457具有抗性的具体基因。在本研究中,我们对绥农2号和大浦这两个韩国大豆品种进行了比较转录组分析,这两个品种分别被鉴定为对大豆疫霉分离株2457具有抗性和敏感性。对接种后0、6和12小时(HAI)采集的组织样本进行了RNA测序,发现在不同时间点以及两个品种之间,防御相关基因的表达存在显著差异。与茉莉酸、水杨酸、乙烯和系统获得性抗性途径相关的基因在两个品种中,在接种后6小时和12小时相比于接种后0小时均上调,并且在接种后6小时和12小时,这些生物学过程在绥农2号中比在大浦中上调得更强。对先前确定的QTL区域内的差异表达基因(DEG)和候选基因进行比较,发现在绥农2号上调的DEG中,特别是在接种后12小时相比于接种后0小时,有一个拟南芥HS1 PRO - 1 2基因的直系同源基因。本研究将有助于有针对性地开展育种工作,以培育出对大豆疫霉具有更强抗性的大豆品种。