KASP primer group related to wheat scab resistance and application of KASP primer group
A technology related to wheat head blight and resistance, applied in the field of crop breeding and molecular biology, can solve problems such as difficulty in using disease-resistant sites, poor agronomic traits, large genetic and physical distances, etc.
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Embodiment 1
[0033] Example 1, Qfhb.3AL17928 molecular marker development:
[0034] In this example, Yangmai 158 and Zhengmai 9023 were used as the female parent and male parent (retained seeds in the laboratory of Jiangsu Academy of Agricultural Sciences), respectively, and a total of 231 recombinant inbred lines F were obtained by single-grain transmission. 5:7 As materials, it was planted in the greenhouse for two consecutive years in 2016–2017 and 2017–2018.
[0035] First sow wheat seeds in 96-hole plug trays. After the seeds absorb water, put the plug trays into the vernalization chamber (6°C) for vernalization for 28 days, then transfer them to the greenhouse and plant them in flower pots. 8 plants are planted in each pot, and each line is planted. 2 pots, randomly arranged. In the first month after planting, set the daytime temperature to 17±2°C and the night temperature to 13±2°C, then set the daytime temperature to 22±5°C and the night temperature to 19±2°C until maturity. Duri...
Embodiment 2
[0044] Example 2, verification of Qfhb.3AL17928 in recombinant inbred lines:
[0045] 231 parts of recombinant inbred line F 5:7 According to the method of Example 1, the wheat sample was carried out by using Qfhb.3AL17928 to carry out KASP marker amplification detection, and the detection results were as follows: figure 2 shown. In Figure 2, the blank control N, the allelic variation g of the disease-resistant SNP, and the allelic variation a of the susceptible SNP are well-typed, and the coincidence rate with the SNP allelic variation in GBS sequencing in Example 1 is 100%. It indicated that KASP markers were successfully developed, and Qfhb.3AL17928 could be further applied to the prediction of scab resistance in wheat samples.
Embodiment 3
[0046] Example 3, verification of Qfhb.3AL17928 in natural populations:
[0047] In order to verify the effectiveness of Qfhb.3AL17928, 74 cultivars or high-generation lines were selected from the middle and lower reaches of the Yangtze River wheat region, and were inoculated with head blight at 3 points for 2 consecutive years. The inoculation method is similar to that of Example 1. The conidia suspension of the strong pathogenicity race F0609 of Fusarium graminearum is selected to inoculate 10 ears of wheat. After inoculation, it is bagged and kept moist for 72 hours. After the inoculation, the disease degree of each ear of wheat is investigated 14 days after the inoculation. Ear number, calculate the sick spikelet number of each variety (line) as the average value of 10 wheat ears, as shown in Table 1.
[0048] Table 1 Allelic variation of Qfhb.3AL17928 SNP and number of diseased spikelets in 74 wheat cultivars (lines)
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[0050]
[0051] Genomic DNA extractio...
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