SSR molecular marker linked with wheat spikelet number QTL and application of SSR molecular marker
A technology of molecular markers and spikelet number, which is applied in the field of molecular biology and crop genetics and breeding, can solve the problem of not many molecular markers, achieve high linkage degree and improve the efficiency of breeding work
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Embodiment 1
[0030] Example 1 Acquisition of wheat spikelet number QTLQSns.sau.3D and its molecular marker gdm8
[0031] 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.
[0032] 2. Phenotypic identification of spikelet number characteristics of recombinant inbred lines
[0033] The number of spikelets of recombinant inbred lines was analyzed and identified at the maturity stage of wheat.
[0034] 3. SSR analysis and DArT analysis
[0035] a) DNA extraction: the DNA of parental Q1028, Zhengmai 9023 and recombinant inbred lines population plants was extracted by CTAB method.
[0036]b) DArT ana...
Embodiment 2
[0047] Example 2 Application of molecular marker gdm8 in identifying spikelet number QTLQSns.sau-3D wheat plants
[0048] 1. Using Tibetan semi-wild wheat Q1028 as the female parent and common wheat line 99E18 as the male parent to construct a recombinant inbred line, and randomly select 8 lines from the offspring lines.
[0049] 2. Carry out gdm8 marker detection to the obtained 8 strains, the specific method is: extract the DNA of 8 strains at the seedling stage; use it as a template, and utilize the primers (SEQIDNo: 1 and 2) of amplifying the molecular marker gdm8 Perform PCR amplification.
[0050] PCR amplification system: 5μL 10×PCR reaction buffer, 1.5UExTaq DNA polymerase, 2mMMgCl 2 , 0.2mMdNTP, 150ng each of upstream and downstream primers, 100ng template DNA, and double-distilled water to a total of 50μL.
[0051] PCR program: pre-denaturation at 94°C for 5 minutes; denaturation at 94°C for 30 s, annealing at 55°C for 45 s, extension at 72°C for 30 s, a total of 3...
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