A screening method, molecular marker, primer and application of a molecular marker linked to a soybean cyst nematode resistance locus
A technology of soybean cyst nematodes and molecular markers, applied in the field of genetic breeding, can solve the problems of heavy workload, less QTL analysis, and difficulty in popularization and application, and achieve remarkable results and reduce the number of cysts
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[0062] Example 2. Screening methods for molecular markers.
[0080] SSR_16_02-F and SSR_16_02-R primer pair obtained molecular marker is SSR_16_02;
[0081] SSR_16_03-F and SSR_16_03-R primer pair obtained molecular marker is SSR_16_03;
[0082] SSR_16_04-F and SSR_16_04-R primer pair obtained molecular marker is SSR_16_04;
[0084] SSR_16_06-F and SSR_16_06-R primer pair obtained molecular marker is SSR_16_06;
[0086] The molecular markers obtained by the SSR_16_08-F and SSR_16_08-R primer pairs are the SSR_16_08 molecular markers.
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[0090] rhg1 and Rhg4 site SNP analysis:
[0096] There is a mutation of cytosine and guanine (C / G) at 108bp on the Rhg4 PCR amplification product (Fig. 8), which is resistant to disease
[0098] a. QTL analysis of cyst nematode race 3 under multiple genetic backgrounds.
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[0109] Samples from this population containing major loci rhg1 and Rhg4 were removed and mapped (Table 7).
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