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Development of a multiallelic SCAR marker for the scab resistance gene Vr1/Vh4/Vx from R12740-7A apple and its utility for molecular breeding

Zugehörigkeit
Federal Centre for Breeding Research on Cultivated Plants, Institute of Fruit Breeding, Dresden, Pillnitzer Platz 3a, Germany
Boudichevskaia, A.;
GND
128593652
Zugehörigkeit
Federal Centre for Breeding Research on Cultivated Plants, Institute of Fruit Breeding, Dresden, Pillnitzer Platz 3a, Germany
Flachowsky, Henryk;
GND
172861896
Zugehörigkeit
Federal Centre for Breeding Research on Cultivated Plants, Institute of Fruit Breeding, Dresden, Pillnitzer Platz 3a, Germany
Peil, Andreas;
Zugehörigkeit
Federal Centre for Breeding Research on Cultivated Plants, Institute of Fruit Breeding, Dresden, Pillnitzer Platz 3a, Germany
Fischer, C.;
GND
1059150336
Zugehörigkeit
Federal Centre for Breeding Research on Cultivated Plants, Institute of Fruit Breeding, Dresden, Pillnitzer Platz 3a, Germany
Dunemann, Frank

A major scab resistance gene initially called Vr1 was identified in the apple cultivar "Regia" derived from the Malus scab resistance source R12740-7A (Russian seedling, RS). A codominant, multiallelic sequence characterized amplified region (SCAR) marker was developed from a random amplified polymorphic DNA marker identified by bulked-segregant analysis. Additional alleles of the AD13 marker locus proved to be informative for the analysis of genetic relationships within Malus including putative relatives of RS. Separate linkage maps were created for the two families derived from crosses with "Regia". Using phenotypic data from the greenhouse scab tests, the recombination frequency between Vr1 and AD13-SCAR was between 6 and 17%. The Vr1 locus appeared to be closely linked to the Vx [Hemmat et al. J Am Soc Hortic Sci, 127:365-370, 2002], Vr2 [Patocchi et al. Theor Appl Genet, 109:1087-1092, 2004], and the Vh4 gene [Bus et al. Mol Breed, 15:103-116, 2005a]. Our linkage analysis of the molecular markers identified by Hemmat et al. [J Am Soc Hortic Sci, 127:365-370, 2002] for two scab resistance factors from RS (Vr and Vx) indicate that both genes are separated by a large distance on apple linkage group 2 [Boudichevskaia et al. Acta Hortic, 663:171-175, 2004]. This is in agreement with the results of Bus et al., [Mol Breed, 15:103-116, 2005a] who concluded that (1) the RS-derived gene Vh2 is identical to Vr, (2) the RS-derived gene Vh4 is identical to Vx and Vr1, (3) Vh2/Vr and Vh4/Vr1/Vx map on opposite sides of LG 2. One of our main goals was the verification of the Vr1-SCAR within a practical apple-breeding program. The utility of the AD13-SCAR was evident after 2 years under natural scab infection conditions in both families investigated. This is the first report about the confirmation of a molecular marker for a RS resistance factor in a 2-year field experiment. A multiplex polymerase chain reaction assay based on two codominant SCARs for Vf and Vr1 was tested in an apple progeny segregating for both genes. The result of the two-marker approach is discussed with respect to scab races, which are able to overcome the Vf resistance gene.

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