QTL for resistance to wheat powdery mildew in adult stage and molecular marker thereof
A technology of wheat powdery mildew and molecular markers, which is applied in the field of wheat genetics and breeding, can solve the problems of slow selection speed and the like, and achieve the effect of improving breeding efficiency
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Embodiment 1
[0024] Example 1 Location of QTL and determination of molecular markers
[0025] NO.1 Experimental materials and methods
[0026] NO.1.1 Experimental materials
[0027] The test material TutoumaiA is a landrace wheat variety that is highly susceptible to various wheat powdery mildew physiological races at the seedling stage and high resistance at the adult plant stage; SY936 is a commonly used cultivar that is highly resistant to powdery mildew at both the seedling stage and the adult plant stage. High sense. In this study, the RIL (recombinant inbred line) population constructed using TutoumaiA and SY936 as parents contained 154 lines.
[0028] NO.1.2 Phenotype identification
[0029] NO.1.2.1 Field test
[0030] The parent and RIL population materials were planted in the agronomy experimental field of the South School of Shandong Agricultural University in 2015, 2016, and 2017 respectively. The on-demand method was adopted, with a plant spacing of 7 cm and a row width ...
Embodiment 2
[0065] Example 2 Detection by Molecular Markers
[0066] NO.1 Genomic DNA extraction of wheat to be tested (CTAB method):
[0067] The specific steps of DNA extraction by CTAB method: (a) Take about 100 mg of young wheat leaves in a 96-well deep-well plate, use a freeze-vacuum dryer to drain the water in the leaf tissue, and then place it in a tissue grinder to grind the leaves into powder; (b) Add 600-800 μL CTAB solution to a 96-well deep-well plate equipped with crushed leaves, then cover the deep-well plate and place it in a water bath at 65°C for 90-120 minutes, during which time shake lightly 3-4 times to fully lyse the DNA; ( c) After the water bath is completed, add 600-800 μL (volume equal to that of CTAB) chloroform isoamyl alcohol (volume ratio 24:1) and shake gently for 10 minutes; (d) Centrifuge at 4000 rad / min for 10 minutes and take about 600 μL of supernatant Place in a new 96-well deep-well plate (note the corresponding serial number); (e) add isopropanol e...
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