Molecular marker primer of rice gall midge-resistant major gene Gm5 and marking method and application of molecular marker primer
A major gene and molecular marker technology, applied in the field of molecular genetics, can solve the problems of difficult introduction and aggregation of insect-resistant genes, complex identification of insect-resistance, etc., and achieve the effects of convenient identification, convenient and rapid detection, and improved screening efficiency.
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Embodiment 1
[0031] Acquisition of molecular markers
[0032] 1. F2 population construction and phenotypic identification
[0033] (1) Indica rice variety ARC5984 is highly resistant to rice gall midge Indian biotypes 1, 2 and 5 (Kumar et al.1998), and ARC5984 is highly resistant to Chinese biotypes 2 and 4 (Wu et al.2014). This insect-resistant variety comes from the Plant Protection Research Institute of Guangxi Academy of Agricultural Sciences. F obtained after 9311 / ARC5984 hybridization experiment 1 The individual re-selfed to obtain F 2 offspring, each F 2 A single plant obtains the corresponding F by selfing 2:3 Families were screened for insect resistance. Insect resistance identification experiments showed that ARC5984 had high resistance to rice gall midge populations from Nanning rice fields;
[0034] (2) Adopt seedling stage inoculation treatment to parents, F 2:3 Families were tested for insect resistance. To ensure that the parent and F 2:3 Each family in the group grow...
Embodiment 2
[0048] Validation of Molecular Markers
[0049] 1. Materials and Methods
[0050] (1) Material
[0051] Negative varieties: susceptible lines (species) 9311 and MH63, both of which are conventional rice materials preserved in our laboratory.
[0052] Positive varieties: high insect-resistant strains (species) ARC5984, 570011 and ARC5833, all of which are conventional rice materials preserved in our laboratory.
[0053] There are 28 offspring of ARC5984×9311 hybrid combination.
[0054] Molecular marker primer: Z22595
[0055] (2) method
[0056] The genomic DNA of rice sample leaf was extracted by CTAB extraction method, the sample DNA was amplified with primer Z22595, and the amplified product was separated by 3% agarose gel electrophoresis (the method is the same as in Example 1).
[0057] 2. Results:
[0058] Using the method above, PCR amplification was performed on the genomic DNA of 33 different samples of rice lines 570011, 9311, and ARC5984, respectively. Such a...
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