Wheat stripe rust-resistant gene QYr.sicau-1B-1 SSR molecular marker and application
A qyr.sicau-1b-1ssr, molecular marker technology, applied in the fields of molecular biology and crop genetics and breeding, can solve the problems of no harvest, inability to perform photosynthesis, yellow leaves of wheat, etc., achieve high linkage degree, improve breeding The effect of work efficiency
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Embodiment 1
[0035] Example 1 Obtainment of Wheat Stripe Rust Resistance Gene QYr.sicau-1B-1 and Its Molecular Marker Xwmc156
[0036] (1) Using '20828' as the female parent and crossing the wheat variety Chuannong 16 as the male parent, the hybrid F1 was obtained. The F1 generation was self-crossed to obtain F2, and 199 individual plants were randomly selected in F2, self-crossed, and harvested separately Single plant, continue selfing in the next year, and repeat this until the F6 generation, and obtain a recombinant inbred line containing 199 lines, constituting a genetic mapping population.
[0037] (2) Identification of stripe rust phenotype in the recombinant inbred line population. When the induced material SY95-71 is fully morbid, the disease resistance response of the test material is recorded in the field, and the response type is classified according to the 1-9 classification standard for each strain in the population. The determination was carried out, and the determination res...
Embodiment 2
[0052] Example 2 Application of Molecular Marker Xwmc156 in Identification of Stripe Rust Resistance QTL QYr.sicau-1B-1
[0053] (1) Use '20828' as the female parent and SY95-71 as the male parent to construct a recombinant inbred line, and randomly select 100 lines from the offspring lines.
[0054] (2) Carry out Xwmc156 marker detection on the obtained 100 strains, the specific method is: extract the DNA of 100 strains at the seedling stage; use it as a substrate, and perform PCR with the specific primer pair of molecular marker Xwmc156 as primers Amplify.
[0055] PCR amplification system: 5μL 10×PCR buffer, 1.5U Ex TaqTM DNA polymerase, 2mmol / lMgCl2, 0.2mmol / L dNTP, 150ng each of upstream and downstream primers, 100ng template DNA, double distilled water to a total of 50μL; Program: Pre-denaturation at 94°C for 5 minutes; denaturation at 94°C for 30s, annealing at 55°C for 30s, and extension at 72°C for 45s, a total of 35 cycles; extension at 72°C for 7 minutes; the obtai...
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