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Molecular mapping in oil radish (Raphanus sativus L.) and QTL analysis of resistance against beet cyst nematode (Heterodera schachtii)

GND
1059150301
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Horticultural and Fruit Crops, Germany
Budahn, Holger;
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Horticultural and Fruit Crops, Germany
Peterka, Herbert;
Zugehörigkeit
Horticulture Department, Faculty of Agriculture, Assiut University, Egypt
Mousa, Magdi Ali Ahmed;
Zugehörigkeit
Beijing Vegetable Research Centre, Academy of Agriculture and Forestry Sciences, Beijing, China
Ding, Yunhua;
Zugehörigkeit
Yunnan Academy of Agricultural Sciences, Biotechnology Research Institute, Kunming, China
Zhang, Shaosong;
Zugehörigkeit
Yunnan Academy of Agricultural Sciences, Biotechnology Research Institute, Kunming, China
Li, Jinbin

The beet cyst nematode (Heterodera schachtii Schmidt) can be controlled biologically in highly infected soils of sugar beet rotations using resistant varieties of oil radish (Raphanus sativus L. ssp. oleiferus DC.) as a green crop. Resistant plants stimulate infective juveniles to invade roots, but prevent them after their penetration to complete the life cycle. The resistance trait has been transferred successfully to susceptible rapeseed by the addition of a complete radish chromosome. The aim of the study was to construct a genetic map for radish and to develop resistance-associated markers. The map with 545 RAPD, dpRAPD, AFLP and SSR markers had a length of 1,517 cM, a mean distance of 2.8 cM and consisted of nine linkage groups having sizes between 120 and 232 cM. Chromosome-specific markers for the resistance-bearing chromosome d and the other eight radish chromosomes, developed previously from a series of rapeseed-radish addition lines, were enclosed as anchor markers. Each of the extra chromosomes in the addition lines could be unambiguously assigned to one of the radish linkage groups. The QTL analysis of nematode resistance was realized in the intraspecific F2 mapping population derived from a cross between varieties ‘Pegletta’ (nematode resistant) x ‘Siletta Nova’ (susceptible). A dominant major QTL Hs1 Rph explaining 46.4% of the phenotypic variability was detected in a proximal position of chromosome d. Radish chromosome-specific anchor markers with known map positions were made available for future recombination experiments to incorporate segments carrying desired genes as Hs1 Rph from radish into rapeseed by means of chromosome addition lines.

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