Assessment of DNA markers for seed contamination testing and selection of disease resistance in cabbage

被引:6
|
作者
Kawamura, Kazutaka [1 ]
Shimizu, Motoki [2 ]
Kawanabe, Takahiro [3 ]
Pu, Zujing [1 ]
Kodama, Taro [1 ]
Kaji, Makoto [4 ]
Osabe, Kenji [5 ]
Fujimoto, Ryo [6 ]
Okazaki, Keiichi [1 ]
机构
[1] Niigata Univ, Grad Sch Sci & Technol, Niigata 9502181, Japan
[2] Iwate Biotechnol Res Ctr, 22-174-4 Narita, Kitakami, Iwate 0240003, Japan
[3] Kyoto Sangyo Univ, Fac Life Sci, Kita Ku, Kyoto 6038555, Japan
[4] Watanabe Seed Co Ltd, Misato Cho, Machiyashiki, Miyagi 9870003, Japan
[5] Okinawa Inst Sci & Technol Grad Univ, Plant Epigenet Unit, Okinawa 9040495, Japan
[6] Kobe Univ, Grad Sch Agr Sci, Nada Ku, Kobe, Hyogo 6578501, Japan
基金
日本科学技术振兴机构;
关键词
Brassica oleracea; Marker assisted selection; Clubroot disease; Fusarium yellows; SSR marker; S haplotype; FUSARIUM YELLOWS RESISTANCE; BRASSICA-OLERACEA; CLUBROOT RESISTANCE; CHINESE-CABBAGE; S-HAPLOTYPES; MICROSATELLITE MARKERS; GENETIC PURITY; SSR MARKERS; IDENTIFICATION; POLYMORPHISM;
D O I
10.1007/s10681-016-1821-0
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Cabbage (Brassica oleracea L. var. capitata) is an important vegetable worldwide. Most Japanese commercial cultivars of cabbage use an F-1 hybrid seed production system. The purity of F-1 hybrid seeds is important and the assessment of purity based on DNA markers can be highly accurate. In addition, selection of agronomically important traits such as disease resistance based on DNA markers is useful for breeding of cabbage. The aim of this study is to demonstrate the effectiveness of DNA marker-assisted selection in cabbage. In this study we distinguished the parental S haplotypes in 35 F-1 hybrid cultivars by combining several linked DNA markers. Thirty-one highly polymorphic simple sequence repeats (SSR) markers were screened from 175 reported SSR markers, which are useful for assessment of the purity of F-1 hybrid seeds. We examined the relationship between the DNA marker based genotype and the phenotype by an inoculation test of clubroot disease. A co-dominant PCR-RFLP marker was developed for selection of Fusarium yellows resistance and the genotypes using this marker were consistent with inoculation test in all tested samples.
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页数:14
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