Method for assistantly screening anti-stripe rust wheat, and special primer therefor
A stripe rust and wheat technology, applied in the field of auxiliary screening of stripe rust-resistant wheat, can solve the problems of rust-resistant varieties losing disease resistance, accelerating the directional selection of pathogenic bacteria races, etc.
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Embodiment 1
[0024] Example 1, Discovery of Xrga-1 and rgga-1
[0025] Zhou 8425B showed moderate resistance (IT=2) to high resistance (IT=1) to Tiaozhong 32 at the seedling stage, and high resistance (IT=1) at the adult stage. Both the spring seedling stage and adult plant stage in China were highly sensitive to Tiaozhong 32 (IT=4).
[0026] F 1 group, F 1 The population is 35 individual plants. Will F 1 F 2 group. f 2 The population is 522 individual plants.
[0027] 1. Acquisition of special primer pairs
[0028] in F 2 In a single plant, 20 seedling reaction types were selected as 2, and the 7 SSR marker genotypes linked to the disease-resistant gene on the 7BL chromosome were all mixed with the DNA of a single plant consistent with the disease-resistant parent Zhou 8425B in equal amounts, as an anti- pool. in F 2From a single plant, 20 seedling stage response types were selected as 4, and the 7 SSR marker genotypes on the 7BL were all mixed with the DNA of a single plant c...
Embodiment 2
[0046] The application of embodiment 2, Xrga-1 and rga-1
[0047] Zhoumai 11, Zhoumai 12, Zhoumai 13, Zhoumai 16, Zhoumai 17, Zhoumai 22, Aikang 58, 04-zhong 36, Fu 98-46 and Luomai 22 are descendants of Zhou 8425B (Zhuang Qiaosheng Editor-in-Chief, Chinese Wheat Variety Improvement and Pedigree Analysis, Beijing / China Agricultural Press, 2003.1).
[0048] 1. Detect whether different varieties of wheat carry rga-1
[0049] The genomic DNA of each variety of wheat was extracted, and the genomic DNA was used as a template to carry out PCR amplification with Xrga-1 respectively.
[0050] The 15 μl PCR reaction system is: 20ng template DNA, 150 μM dNTPs (TaKaRa Company), 0.25U Taq DNA polymerase (Promega Company), 7 pmol of upstream and downstream primers, 1.5 μl 10×PCR buffer (Promega Company), 1.5 mM MgCl 2 (Promega Corporation).
[0051] The PCR reaction was carried out on a PTC-200 PCR amplification instrument. The amplification program was: pre-denaturation at 95°C for 5 ...
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