Wheat spike density QTL linked HRM (high resolution melting) molecular marker and application thereof
A molecular marker, wheat technology, applied in the fields of molecular biology and crop genetics and breeding, can solve the problem that the research on ear density is still less
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Embodiment 1
[0032] Example 1 Acquisition of wheat spikelet number QSd.sau-7A and its molecular marker 0C32-715
[0033] 1. The female parent of Tibetan semi-wild wheat Q1028 was crossed with the wheat variety Zhengmai 9023 as the male parent to obtain the hybrid F1. F1 was self-crossed to obtain F2, and 186 individual plants were randomly selected in F2 for self-crossing. Harvest a single plant, continue selfing in the next year, and repeat this until the F8 generation, and obtain recombinant inbred lines containing 186 lines to form a genetic mapping population.
[0034] 2. Phenotypic identification of panicle density characteristics of recombinant inbred lines
[0035] Phenotypic identification of panicle length and spikelet number of recombinant inbred lines at wheat maturity stage.
[0036] 3. DNA extraction: The DNA of parent Q1028, Zhengmai 9023 and recombinant inbred lines population plants was extracted by CTAB method.
[0037] 4. Use comparative genomics methods to compare with...
Embodiment 2
[0044] Example 2 Application of Molecular Marker OC32-715 in Identifying Ear Density QTLQSd.sau-7A Wheat Plants
[0045] 1. The offspring QZ2 in the RIL population of (Q1028×Zhengmai 9023) was used as the female parent, and the common wheat line Zhengmai 9023 was used as the male parent to construct recombinant inbred lines, and 8 lines were randomly selected from the offspring lines.
[0046] 2. Perform OC32-715 marker detection on the obtained 8 strains, the specific method is: extract the DNA of the 8 strains at the seedling stage; use it as a template to perform fluorescent quantitative PCR on the molecular marker 0C32-715.
[0047] PCR amplification system: 5 μL of SsoFast EvaGreen supermix, 300 ng of upstream primer and 300 ng of downstream primer, 100 ng of template DNA, Dnaes / RNase-free deionized water to a total of 10 μL.
[0048] Fluorescent quantitative PCR amplification program: pre-denaturation at 95°C for 5 minutes; denaturation at 94°C for 15 s, annealing at 59....
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