A functional marker and its application for rapid detection of powdery mildew resistance gene of A. tachyphylla
A powdery mildew resistance gene and a technology of goat grass, applied in the field of wheat genetics and molecular breeding, can solve problems such as difficult to apply breeding
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Embodiment 1
[0019] Example 1 Construction and fine positioning of mapping populations
[0020] 1.1 Materials
[0021] The disease-resistant A. tachyphylla 2147 was used as the parent to cross the susceptible A. tachyphyllum AL8 / 78 to obtain F 1 , 4299 strains of F 2 , further self-intersection, get the corresponding F 2:3 family line;
[0022] 1.2 Method
[0023] 1.2.1F 2 Identification of Powdery Mildew Resistance in Population Seedling Stage
[0024] Will F 2 The populations were planted in small plastic pots of 6cm×6cm and placed in light incubators. The conditions were set as follows: temperature 19°C, humidity 80%, light 2000LUX, 12h; temperature 17°C, humidity 80%, darkness, 12h. Inoculate with E09 strain at the one-heart-one-leaf stage. The inoculation method is the sweeping method. Investigate the condition after 7-10 days. Disease resistance classification adopts 6-level classification method:
[0025] Type 0, immunity, no lesions on plants;
[0026] 0; type, near imm...
Embodiment 2
[0052] Example 2 Ml2147 Map-based cloning and development of functional markers
[0053] 2.1 Materials
[0054] Using the 9 key recombinants screened in the process of fine mapping, we further designed markers and encrypted the linkage map.
[0055] 2.2 Method
Embodiment 1)
[0057] 2.2.2 Developing markers, encrypting fine-positioning linkage map (see Example 1 for specific methods of developing and screening markers)
[0058] 2.2.3 Develop feature flags
[0059] (1) After finding a candidate gene, design primers to amplify the full length of the gene based on the gene sequence information 2147- qc-1 , the upstream sequence of the primer 2147-qc-1 F is: CGGATGGACGCGCCTTCG, downstream sequence 2147-qc-1 R is: GTACTCTAGTGGCACCTTAAACCGG. The gene fragments in 180 natural populations of A. tachyphylla were amplified, sequenced and compared.
[0060] The specific steps for amplifying the gene are as follows:
[0061] a. take wheat or goat grass DNA as PCR amplification template, with 2147-qc-1 As primers, carry out PCR amplification, and the reaction system is 50 μl. The above reaction system specifically includes: 50-100ng / μl DNA 4μl, 25μl 2×GC buffer (containing Mg 2+ ), 4 μl ldNTP, 1.0 μl each of upper and lower primers, 1 μl LA-Taq DNA ...
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