Method for screening stripe rust resisting wheat and its special primer
A stripe rust and wheat technology, applied in the field of screening stripe rust-resistant wheat, can solve the problems of loss of disease resistance, accelerate the directional selection of pathogen races, etc., and achieve the effect of prolonging disease resistance
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Embodiment 1
[0018] Example 1. Obtainment of SSR markers Xcfa2040 and Xbarc32 of new wheat stripe rust resistance genes and identification of gene sources
[0019] 1. Obtainment of SSR markers Xcfa2040 and Xbarc32 for the new wheat stripe rust resistance genes
[0020] Using the currently popular stripe rust race CYR32 in China to test the F of wheat material Zhou 8425B and China Spring (parent) 1 , F 2 And F 3 Seedling resistance identification of the generation population, a total of F 1 Population 8 strains, F 2 Population 611 strains, F 3 97 strains of the family, the results are shown in Table 1, F 1 All disease resistance, F 2 Anti-sense separation meets 3∶1(x 2 =2.91, P>0.05), F 3 The ratio of family separation is homozygous anti-influence separation: homozygous anti-influence = 1:2:1 (x 2 =1.268, P>0.5), indicating that Zhou 8425B contains a dominant disease resistance gene. Twenty typical disease-resistant plants and 10 susceptible plants were selected to form a disease-resistant pool...
Embodiment 2
[0031] Example 2: Screening of wheat resistant to stripe rust with Xcfa2040 and Xbarc32 molecular markers
[0032] Experimental wheat varieties: Lianfeng No. 1, Shanqianmai, St2422 / 464 and Annong 7959
[0033] Plant the above-mentioned wheat varieties according to the conventional method. After harvesting the grains, extract the genomic DNA of each wheat variety, and then use it as a template, respectively under the guidance of a primer pair consisting of the upstream and downstream nucleotide sequences of primers cfa2040 and barc32 in the sequence table, Perform PCR amplification. The 20μl PCR reaction system is: template DNA 60ng, Taq enzyme 1U (Beijing Tianwei Times Company), upstream and downstream primers (2μmol·L -1 ) 1.5μl each, dNTPs (25μmol·L -1 ) 0.2μl, 2μl of 10×PCR buffer, supplement the reaction system to 20μl with sterile distilled water. The PCR reaction program is: first 94℃ 4min; then 94℃ 40s, 55℃ 1min, 72℃ 1min, a total of 35 cycles; finally 72℃ 10min, 4℃ storage...
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