Genetic analysis of clubroot resistance in Chinese cabbage using single spore isolate of Plasmodiophora brassicae and development of RAPD marker linked to its resistance gene

  • Cho, Kwang-Soo (Horticulture Dept., National Institute of Highland Agriculture, RDA) ;
  • Hong, Su-Young (Horticulture Dept., National Institute of Highland Agriculture, RDA) ;
  • Han, Young-Han (Horticulture Dept., National Institute of Highland Agriculture, RDA) ;
  • Yoon, Bong-Kyeong (Horticulture Dept., National Institute of Highland Agriculture, RDA) ;
  • Ryu, Seoung-Ryeol (Horticulture Dept., National Institute of Highland Agriculture, RDA) ;
  • Woo, Jong-Gyu (Horticultural Biotechnology Dept., National Horticulture Research Institute, RDA)
  • Published : 2008.06.30

Abstract

To identify inheritance of clubroot disease resistance genes in Chinese cabbage, seedling tests of $BC_1P_1,\;BC_1P_2$, and $F_2$ populations derived from $F_1$ hybrid(var. CR Saerona) using single spore isolate(race 4 identified with William's differential host) from Plasmodiophora brassciae were conducted. Resistance(R) and susceptible(S) plants segregated to 1:0 in backcross to the resistant parent. The $F_2$ population segregated in a 3(R):1(S) ratio. This result implied that the resistance of clubroot disease is controlled by a single dominant gene to the race 4 of P. brassicae in CR Saerona. To develop DNA markers linked to clubroot resistance genes, 185 plants of CR Saerona among $F_2$ populations were used. A total of 300 arbitrary decamer was applied to $F_2$ population using BSARAPD(Bulked segregant analysis-Randomly amplified polymorphic DNA). One RAPD marker linked to clubroot resistance gene in CR Saerona($OPJ_{1100}$) was identified. This marker was 3.1 cM in distance from resistance gene in $F_2$ population. This marker may be useful for a marker-assisted selection(MAS) and gene pyramiding of the clubroot disease resistant gene in Chinese cabbage breeding programs.

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