Major QTL for regulating and controlling resistance of sogatella furcifera of rice, molecular marker and application
A white-backed planthopper and molecular marker technology, applied in the field of rice breeding and molecular biology, can solve the problems of fine positioning and limited research on related molecular markers, and achieve the effect of speeding up the selection and breeding process
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Embodiment 1
[0033] Example 1 Mapping of major QTLs regulating rice white-backed planthopper resistance
[0034] 1. Acquisition of experimental materials
[0035] Reyan 2 was used as the donor parent, and the rice variety Huazhan was used as the recipient parent for crossing, and the single-seed method was used (that is, F1 was treated with bagging and planting a single plant until the phenotype of the offspring lines did not segregate). , and finally got 120 stable genetic lines (F13, all lines are phenotypically stable), forming a recombinant inbred line RIL population, such as figure 1 .
[0036] Select 60 seeds (F13) of the parent and each strain, soak the seeds for 2 days after surface disinfection, wrap them in a moist towel, put them in a 37°C incubator for 48 hours, and select the seeds with consistent dew and whiteness for sowing. After 30 days, the parents with similar growth conditions and 24 seedlings of each line were selected for transplantation. All rice materials were pla...
Embodiment 2
[0043] Example 2 Molecular marker-assisted selection
[0044] Molecular markers IndelWbph-1 and molecular markers IndelWbph-2 were set at the upstream and downstream of the QTL locus qWBPH-3, respectively, and primers were designed;
[0045] The primer pair for molecular marker Indel Wbph-1 is:
[0046] Upstream primer: 5'-GGCTATTATGTACACTGCAGCA-3', SEQ ID NO.1;
[0047] Downstream primer: 5'-CTGGATCGGCAGGCGTAG-3', SEQ ID NO.2;
[0048] The primer pair for molecular marker Indel Wbph-2 is:
[0049] Upstream primer: 5'-TCGAACCGCTCCATCCATTT-3', SEQ ID NO.3;
[0050] Downstream primer: 5'-TTGGCCATGGAAGGAGGG-3', SEQ ID NO.4.
[0051] Genomic DNA was extracted from the rice leaves of parents Reyan 2, Huazhan and its F1 generation and RIL population, and PCR amplification was performed on the genomic DNA using the above molecular markers;
[0052] PCR reaction system: 1 μL of upstream primer (10 μmol), 1 μL of downstream primer (10 μmol), 2 μL of DNA template (>100 ng / μL), 6 μL o...
Embodiment 3
[0057] Example 3 Application of QTLs related to rice white-backed planthopper resistance in rice breeding
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