Screening method of molecular marker linked with soybean cyst nematode resistance locus, molecular marker, primers and application
A technology of molecular markers and cyst nematodes, applied in the field of genetic breeding, can solve the problems of high operator experience requirements, less QTL analysis, and difficulty in popularization and application
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Embodiment 1
[0052] Example 1. Soil propagation and resistance identification of soybean cyst nematode disease.
[0053] In this study, the recombinant inbred line populations constructed from the three combinations of Heinong 37×Dongnong L-10, Suinong 10×Dongnong L-10, and Suinong 14×Dongnong L-10 were evaluated against soybean cyst nematodes. For the identification of the resistance of No. 3 physiological race, the acquisition process of the recombinant inbred line population is as follows: through the self-propagation of the F1 generation single grain derived from the above-mentioned parental combination hybridization to obtain the F2 generation single grain, continuous selfing from the F2 generation, combining The offspring were reserved to the F6 generation by the single seed transmission method, and the line propagation was carried out from the F6 generation to the F11 generation. The map construction and disease resistance identification of the F11 generation were carried out, and th...
Embodiment 2
[0062] Example 2. Screening method for molecular markers.
[0063] Molecular marker analysis of parents and offspring:
[0064] (1) The soybean variety Dongnong L-10 was used as the male parent, and the soybean varieties Heinong 37, Suinong 10, and Suinong 14 were used as the female parents, and the recombinant inbred line F was obtained after crossing 5:11 Generation: Heinong 37×Dongnong L-10, Suinong 10×Dongnong L-10, Suinong 14×Dongnong L-10; See Example 1 for the breeding method of the recombinant inbred lines.
[0065] (2) Extract the parental genome DNA of Dongnong L-10, Heinong 37, Suinong 10, and Suinong 14 respectively, and use SSR primers for PCR amplification to screen polymorphic SSR primers; the method is as follows:
[0066]According to the previous report on soybean cyst nematode resistance loci in this study, the SSR marker loci in the target QTL (qSCN16) segment (31.46Mb-35.79Mb) on Chr.16 (LGJ) linkage group of soybean chromosome 16 were selected Spot, and ...
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