Molecular marker-assisted breeding method of gibberellic disease-resistant high-yield wheat
A molecular marker-assisted, scab-blight technology, applied in the fields of botanical equipment and methods, biochemical equipment and methods, and microbial assay/inspection to achieve the effect of improving breeding efficiency
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Embodiment 1
[0034] Example 1 A molecular marker-assisted breeding method for scab-resistant high-yield wheat
[0035] Parent selection: use the CTAB method to extract DNA from mixed leaves of wheat varieties with a cumulative extension area of more than 5 million mu, good comprehensive disease resistance and comprehensive agronomic traits, or their derivative varieties (lines) at the seedling stage, and molecular markers to screen out the number of grains carried at the same time The female target variety Zhenmai 9 of the synergistic site QGns-3B and the grain weight synergistic site QGW-Y4; and the male target variety Yangmai 18 carrying the main genes Fhb1 and Fhb5 for resistance to head blight were screened out.
[0036] In the screening results, it was found that "wheat varieties with a cumulative promotion area of more than 5 million mu, excellent agronomic traits, and good comprehensive disease resistance or their derivative varieties (lines)" Zhenmai 9, Zhenmai 12, Yangmai 16, a...
Embodiment 2
[0045] Example 2 Establishment of molecular marker-assisted selection of grain number per spike locus QGns-3B and scab resistance gene Fhb5
[0046] The primer sets of molecular markers Xgpw1145, stm7tgag, WMC752, and MAG9482 were used to detect whether the materials in steps 1), 4) and 5) in Example 1 carried the grain number per spike site QGns-3B and the head blight resistance gene Fhb5.
[0047] 1. With the genomic DNA extracted in step 1) as a template, use the QGns-3B site linkage marker Xgpw1145 and stm7tgag for detecting wheat ear grain number synergistic sites to carry out PCR amplification to obtain the amplified product, and determine the QGns-3B site The target material Zhenmai No. 9 with the same genotype as Yangmai 17 was selected; the linkage markers WMC752 and MAG9482 used to detect wheat head blight resistance gene Fhb5 were used for PCR amplification to obtain the amplified product, and the Fhb5 locus was determined to be related to Wangshuibai The target mat...
Embodiment 3
[0055] Example 3 Establishment of molecular marker-assisted selection method for scab resistance gene Fhb1
[0056] The primer set of molecular marker TaHRC-GSM was used to detect whether the materials in steps 1), 4) and 5) in Example 1 carried the head blight resistance site Fhb1.
[0057] 1, with the genomic DNA extracted in step 1) as a template, the linkage marker TaHRC-GSM that is used to detect the scab-resistant gene of wheat described in Example 1 is used to carry out PCR amplification, obtain the amplified product, and determine the Fhb1 site and The genotype of Sumai 3 is the same as the target material Yangmai 18.
[0058] 2. Extract Zhenmai No. 9, Yangmai 18 and F by CTAB method 3 single plant, F 4 Genomic DNA from the leaves was mixed in the plant row and diluted to obtain a template solution with a DNA concentration of about 30 ng / μL.
[0059] The sequence of the specific primer set of the linked GSM marker for the detection of scab resistance gene Fhb1 by mo...
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