Identification method and special marker for red feather mutagenic genotype of white leghorn
A genotype and heterozygous genotype technology is applied in the field of identification of genotypes caused by red feathers in White Leghorn chickens and special markers. It does not show problems such as red feather phenotype, and achieves the effect of saving breeding cost and time, increasing variety benefits and improving use value.
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Embodiment 1
[0053] Example 1. Discovery of causative mutations in Bailaihang chicken red feathers and preparation of amplification primers and establishment of methods
[0054] 1. Discovery of the causative mutation in the red feather of Bailaihang chicken
[0055] 1. Extract the genomic DNA of the chicken to be tested
[0056] Using 2000 Beijing Huadu Yukou Poultry Industry Co., Ltd. Bailaihang strain hens to cross with Luodao red roosters, the feather color phenotypes of the hybrid offspring were counted, and the number of offspring hens was more than 5 and 100% were red feathers. 9 aircraft carrier chickens were used as the red feather group, and 9 white aircraft carrier chickens with more than 5 offspring hens and 100% white feathers were selected as the white feather group; these two groups were used as chickens to be tested.
[0057] Blood was collected from the wing veins of the chickens to be tested, treated with anticoagulants, lysed and digested with protease, and then the geno...
Embodiment 2
[0112] Example 2. Identifying the genotype of the causative mutation in the red feather of the White Legion chicken to be tested by using the SNP loci of the red feather of the White Legion chicken
[0113] 1. Use the SNP loci of Bailaihang chicken red feather to identify the genotype of the causative mutation in Bailaihang chicken red feather
[0114] 1. Genomic DNA extraction
[0115] Genomic DNA of 1573 Bailai aircraft carrier chickens to be tested was extracted.
[0116] 2. PCR amplification
[0117] Using the genomic DNA of 1,573 white-born aircraft carrier chickens to be tested as templates, PCR amplification was carried out by the method described above in Example 1 to obtain the PCR amplification products of each chicken to be tested.
[0118] 3. Sequencing and analysis
[0119] The PCR amplification products of the above-mentioned chickens to be tested were subjected to DNA Sanger sequencing analysis, and the sequencing result of the PCR was sequence 1. According t...
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