霜霉病
生物
数量性状位点
甜瓜
遗传学
基因分型
人口
基因定位
植物抗病性
分子育种
等位基因
遗传连锁
标记辅助选择
基因
基因型
园艺
染色体
人口学
社会学
作者
Xuejun Zhang,Yueming Ling,Wenli Yang,Minghua Wei,Zhenzhu Wang,Meihua Li,Yong Yang,Bin Liu,Hongping Yi,Yang‐Dong Guo,Qiusheng Kong
标识
DOI:10.3389/fpls.2023.1202775
摘要
Downy mildew (DM) is a major foliar disease globally causing great economic loss in melon production. Utilizing disease-resistant cultivars is the most efficient approach for disease control, while discovery of disease-resistant genes is crucial for the success of DM-resistant breeding. To address this problem, two F 2 populations were constructed using the DM-resistant accession PI 442177 in this study, and QTLs conferring DM resistance were mapped using linkage map and QTL-seq analysis, respectively. A high-density genetic map with the length of 1096.7 cM and density of 0.7 cM was generated by using the genotyping-by-sequencing data of a F 2 population. A major QTL DM9.1 with the phenotypic variance explained proportion of 24.3-37.7% was consistently detected at the early, middle, and late growth stages using the genetic map. QTL-seq analyses on the two F 2 populations also validated the presence of DM9.1 . Kompetitive Allele-Specific PCR (KASP) assay was further carried out to fine map DM9.1 into 1.0 Mb interval. A KASP marker co-segregating with DM9.1 was successfully developed. These results not only provided valuable information for DM-resistant gene cloning, but also offered useful markers for melon DM-resistant breeding programs.
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