Department of Horticulture and Institute of Plant Breeding, Genetics & Genomics, The University of Georgia, Tifton, GA, 31793, USA.
Center for Applied Genetic Technologies and Institute of Plant Breeding, Genetics & Genomics, The University of Georgia, Athens, GA, 30602, USA.
Sci Rep. 2017 May 2;7(1):1317. doi: 10.1038/s41598-017-00971-6.
Resistance to root-knot nematode was introgressed into cultivated peanut Arachis hypogaea from a wild peanut relative, A. cardenasii and previously mapped to chromosome A09. The highly resistant recombinant inbred RIL 46 and moderately resistant RIL 48 were selected from a population with cv. Gregory (susceptible) and Tifguard (resistant) as female and male parents, respectively. RNA-seq analysis was performed on these four genotypes using root tissue harvested from root-knot nematode infected plants at 0, 3, 7 days after inoculation. Differential gene expression analysis provides evidence that root-knot nematodes modulate biological pathways involved in plant hormone, defense, cell signaling, cytoskeleton and cell wall metabolism in a susceptible reaction. Corresponding to resistance reaction, an effector-induced-immune response mediated by an R-gene was identified in Tifguard. Mapping of the introgressed region indicated that 92% of linkage group A09 was of A. cardenasii origin in Tifguard. RIL46 and RIL 48 possessed 3.6% and 83.5% of the introgression on A09, respectively. Within the small introgressed region carried by RIL 46, a constitutively expressed TIR-NBS-LRR gene was identified as the candidate for nematode resistance. Potential defense responsive pathways include effector endocytosis through clathrin-coated vesicle trafficking, defense signaling through membrane lipid metabolism and mucilage production.
对根结线虫的抗性已从野生花生 Arachis cardenasii 导入栽培花生 Arachis hypogaea,并先前被映射到染色体 A09。高度抗性的重组自交系 RIL 46 和中度抗性的 RIL 48 是从以 cv. Gregory(敏感)和 Tifguard(抗性)为母本和父本的群体中选择的。使用来自根结线虫感染植物的根组织,在接种后 0、3、7 天对这四种基因型进行了 RNA-seq 分析。差异基因表达分析表明,根结线虫在感病反应中调节植物激素、防御、细胞信号转导、细胞骨架和细胞壁代谢相关的生物途径。与抗性反应相对应,在 Tifguard 中鉴定到了由效应物诱导的免疫反应,该反应由 R 基因介导。导入区域的图谱表明,在 Tifguard 中,A09 的 92% 来自 A. cardenasii。RIL46 和 RIL 48 分别在 A09 上具有 3.6%和 83.5%的导入片段。在 RIL 46 携带的小导入片段内,鉴定到一个组成型表达的 TIR-NBS-LRR 基因作为线虫抗性的候选基因。潜在的防御响应途径包括通过网格蛋白包被小泡运输进行效应物内吞作用、通过膜脂代谢和粘液产生进行防御信号传递。