Rice brown planthopper resistant major gene Bph30 molecular marker and application thereof
A technology of resisting brown planthopper and main gene, applied in the field of molecular genetics, can solve environmental problems such as rice pollution
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Embodiment 1
[0060] [Example 1] Acquisition of a molecular marker closely linked to the main gene Bph30 for resistance to brown planthopper in rice
[0061] (1) Segregation population construction and phenotypic identification
[0062] (1) In 1979, the International Rice Research Institute (RRI) found that the rice variety AC1613 was resistant to three brown planthopper populations (biotypes 1, 2, and 3) through insect resistance screening. In 2013, it was identified by the seedling stage group method. The resistance of the variety to brown planthopper was found to be highly resistant to the brown planthopper population in Wuhan, and the resistance level was level 1. In order to locate the resistance gene and find simple and effective molecular markers closely linked to the gene, the present invention uses the susceptible variety 9311 as the female parent and the brown planthopper resistant variety AC1613 as the male parent to cross, and the obtained F 1 ;F 1 F 2 Segregation Groups, Par...
Embodiment 2
[0088] [Example 2] Verification of molecular markers
[0089] 1. Materials and methods
[0090] 1.1 Materials
[0091] Resistant parent AC1613, susceptible parent 9311, two heterozygous 9311 / AC1613BC in the positioning interval 2 f 2 Groups (B4-25, B4-28) have 84 and 75 trees respectively.
[0092]Molecular marker primers: RM16290, SSR-28, RM16294, SSR-68, SSR-69, RM16299, Indel-15, Indel-16, SSR-35, RM16303.
[0093] 1.2 Method
[0094] The resistant parent AC1613, the susceptible parent 9311 and two BC 2 f 2 The phenotype of each individual plant of the population (the method is the same as in Example 1).
[0095] Genomic DNA of rice sample was extracted by CTAB extraction method (method is the same as in Example 1). Sample DNA was amplified with primers RM16290, SSR-28, RM16294, SSR-68, SSR-69, RM16299, Indel-15, Indel-16, SSR-35, RM16303, respectively. The reaction system included 0.10 μM primers, 250 μM dNTPs, 1× PCR reaction buffer (50 mM KCl, 10 mM Tris-HCl pH8...
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