Fujian Provincial Key Laboratory of Plant Molecular and Cell Biology, State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, Fujian Agriculture and Forestry University, Fuzhou, 350002, Fujian, China.
College of Crop Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, Fujian, China.
Theor Appl Genet. 2020 Jul;133(7):2239-2257. doi: 10.1007/s00122-020-03594-0. Epub 2020 Apr 13.
Two novel resistant QTLs mapped and candidate genes identified for Aspergillus flavus resistance in cultivated peanut using SLAF-seq. Aflatoxin contamination in peanuts caused by Aspergillus flavus is a serious food safety issue for human health around the world. Host plant resistance to fungal infection and reduction in aflatoxin are crucial for mitigating this problem. Identification of the resistance-linked markers can be used in marker-assisted breeding for varietal development. Here we report construction of two high-density genetic linkage maps with 1975 SNP loci and 5022 SNP loci, respectively. Two consistent quantitative trait loci (QTL) were identified as qRAF-3-1 and qRAF-14-1, which located on chromosomes A03 and B04, respectively. QTL qRAF-3-1 was mapped within 1.67 cM and had more than 19% phenotypic variance explained (PVE), while qRAF-14-1 was located within 1.34 cM with 5.15% PVE. While comparing with the reference genome, the mapped QTLs, qRAF-3-1 and qRAF-14-1, were located within a physical distance of 1.44 Megabase pair (Mbp) and 2.22 Mbp, harboring 67 and 137 genes, respectively. Among the identified candidate genes, six genes with the same function were found within both QTLs regions. In addition, putative disease resistance RPP13-like protein 1 (RPP13), lipoxygenase (Lox), WRKY transcription factor (WRKY) and cytochrome P450 71B34 genes were also identified. Using microarray analysis, genes responded to A. flavus infection included coding for RPP13, pentatricopeptide repeat-containing-like protein, and Lox which may be possible candidate genes for resistance to A. flavus. The QTLs and candidate genes will further facilitate marker development and validation of genes for deployment in the molecular breeding programs against A. flavus in peanuts.
利用 SLAF-seq 技术定位和鉴定栽培花生抗黄曲霉的两个新抗性 QTLs 及其候选基因。黄曲霉侵染花生导致的黄曲霉毒素污染是全球范围内一个严重的食品安全问题。宿主植物对真菌侵染的抗性和降低黄曲霉毒素含量对于缓解这一问题至关重要。鉴定与抗性相关的标记可用于品种开发的标记辅助选择。本研究构建了两个高密度遗传连锁图谱,分别包含 1975 个 SNP 标记和 5022 个 SNP 标记。鉴定到两个一致的数量性状位点(QTL),分别命名为 qRAF-3-1 和 qRAF-14-1,分别位于第 A03 和 B04 染色体上。QTL qRAF-3-1 被定位在 1.67cM 范围内,解释了超过 19%的表型变异(PVE),而 qRAF-14-1 位于 1.34cM 范围内,解释了 5.15%的 PVE。与参考基因组相比,定位的 QTL qRAF-3-1 和 qRAF-14-1 在物理距离上分别为 1.44 兆碱基对(Mbp)和 2.22 Mbp,分别包含 67 和 137 个基因。在鉴定的候选基因中,有 6 个具有相同功能的基因位于两个 QTL 区域内。此外,还鉴定到假定的抗病蛋白 RPP13 样蛋白 1(RPP13)、脂氧合酶(Lox)、WRKY 转录因子(WRKY)和细胞色素 P450 71B34 基因。利用微阵列分析,发现对黄曲霉侵染有反应的基因包括 RPP13、五肽重复蛋白编码基因和 Lox,它们可能是抗黄曲霉的候选基因。这些 QTL 和候选基因将进一步促进标记的开发和验证,为花生中抗黄曲霉的分子育种计划提供基因资源。