Method for detecting rose cockscomb character
A technology for roses and traits, applied in biochemical equipment and methods, microbial measurement/testing, DNA/RNA fragments, etc., can solve the problems of inability to accurately distinguish dominant homozygous and heterozygous individuals, low breeding efficiency, etc. Achieve the effects of improving breeding and conservation efficiency, speeding up the breeding process, and high accuracy
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Embodiment 1
[0018] Embodiment 1, establishment of PCR detection method and determination of polymorphic sites
[0019] 1. Genotype analysis
[0020] 1. Experimental materials: The CAU resource family is an experimental group established by the research group of Professor Li Ning of China Agricultural University in 1998 to study the location of QTLs that affect important economic traits of chickens and to find the main gene for cloning. The parents are French star broilers and Taihe silk feathers Silkie. In this experiment, 278 individuals of the F0, F1 and F2 generations of 4 CAU resource families were selected.
[0021] 2. Genomic DNA extraction
[0022] Blood was collected from the wing vein of the 12-week-old chicken, lysed after anticoagulant treatment, digested with proteinase K, extracted with phenolic form, dissolved in TE and stored at -20°C.
[0023] 3. PCR amplification
[0024] Using the genomic DNA extracted in step 2 as a template, the CCDC108 gene was amplified by PCR wi...
Embodiment 2
[0042] Embodiment 2, the application of molecular marker
[0043] 6 breeds with rose crown phenotype (all obtained from Poultry Research of Chinese Academy of Agricultural Sciences , Beijing Poultry Breeding Company) and non-rosecrown phenotypes (including non-rosecrown phenotypes such as single crown and bean crown) were measured, and the specific varieties are shown in Table 2 and Table 3.
[0044] 1. Genomic DNA extraction
[0045] Blood was collected from the wing vein of the 12-week-old chicken, lysed after anticoagulant treatment, digested with proteinase K, extracted with phenolic form, dissolved in TE and stored at -20°C.
[0046] 2. PCR amplification
[0047] Using the genomic DNA extracted in step 1 as a template, the CCDC108 gene was amplified by PCR with primers.
[0048] RosecombF1: 5'-GCCCCTTCCTGAAGCAATA-3' (as shown in SEQ ID NO.1 Show);
[0049] RosecombF2: 5'-GACTCCTTCCATCGCTCAGA-3' (as shown in SEQ ID NO.2 Show);
[0050] RosecombR: 5'-CCTTGTTCCCAGC...
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