Method for improving quality of erect panicle japonica rice and molecular marker
A molecular marker and germplasm technology, applied in the fields of plant genetic improvement, botanical equipment and methods, biochemical equipment and methods, etc., can solve the problems of poor rice quality, time-consuming and labor-intensive breeding methods, etc. Efficient process and stable effect
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Embodiment 1
[0033] Example 1: A method for improving the quality of erect panicle type japonica rice
[0034] like figure 1 As shown, a molecular marker-assisted breeding method for improving the quality of erect panicle type japonica rice provided by the embodiments of the present invention includes:
[0035] S1: F 1 Hybrid;
[0036] S2: Select the target genotype is heterozygous and has excellent agronomic traits F 1 A single plant was backcrossed with Nanjing 46 to obtain BC 1 f 1 Hybrid;
[0037] S3 selects BC whose target genotype is heterozygous and has excellent agronomic traits 1 f 1 BC obtained by backcrossing a single plant with Nanjing 46 2 f 1 Hybrid;
[0038] S4: Select BC whose target genotype is heterozygous and has excellent agronomic traits 2 f 1 A single plant was backcrossed with Nanjing 46 to obtain BC 3 f 1 Hybrid;
[0039] S5: Select BC whose target genotype is heterozygous and has excellent agronomic traits 3 f 1 A single plant was backcrossed with ...
Embodiment 2
[0046] A molecular marker and PCR electrophoresis detection and analysis method for quality improvement of erect panicle type japonica rice:
[0047] (1) DNA extraction
[0048] DNA was extracted from rice leaves by CTAB method.
[0049] (2) Primer design
[0050] Utilize dCAPS software to design primers, the nucleotide sequence of described labeled primers is:
[0051] Forward primer G1-F: 5'-GGACGCAAGAACAGCC-3';
[0052] Reverse primer G1-R: 5'-TTCCACCATAGAAATCAACC-3'
[0053] (3) PCR amplification system:
[0054] Rice genomic DNA 20ng / ul 1.0ul, 10×PCR Buffer 2.0ul, 25mM MgCl 2 2.0ul, 2mMdNTP 2.0ul, 10uM primer 2.0ul, 5U / ul Taq DNA polymerase 0.2ul, ddH 2 O 10.8ul, total system 20ul.
[0055] (4) PCR reaction program:
[0056] Pre-denaturation at 95°C for 5 minutes; denaturation at 94°C for 1 minute, annealing at 55°C for 1 minute, extension at 72°C for 1 minute, 35 cycles; extension at 72°C for 10 minutes.
[0057] (5) Enzyme digestion system:
[0058] 10×Buffer...
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