Molecular marker method of two mutation sites in the 5′ regulatory region of chicken pthlh gene and its application in chicken breeding
A technology of regulatory regions and sites, applied in the field of molecular genetics, can solve the problems of affecting transcription initiation and gene expression, etc.
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Embodiment 1
[0019] Example 1 Chicken PTHLH 5'regulatory region sequence alignment and polymorphic site analysis
[0020] 1. Test materials
[0021] 48 recessive Bailuoke chickens (Shandong Jihua Poultry Breeding Co., Ltd.) were randomly sampled, blood was collected from the wing vein, and the genome was extracted and stored at -20°C.
[0022] 2. Test method
[0023] 2.1 Primer design
[0024] The primer P-PTHLH was designed according to the published red original chicken sequence (GenBank Accession NC_006088.4) (see Table 1 and Seq ID No:1 / Seq ID No:2 for the sequence details). This primer is for studying chicken PTHLH 5'regulation The mutation of the region is specially designed based on the sequence of the red rock fowl registered in the database.
[0025] 2.2 PCR amplification
[0026] The genomes of 48 recessive Bailuoke chickens were randomly selected and amplified by PCR with primer P-PTHLH. The primers are shown in Table 1. The reaction system is 20μL, including 1μL of genomic DNA (50-100ng)...
Embodiment 2
[0033] Example 2 Association analysis of chicken PTHLH5' regulatory region polymorphism with age at the start of laying and egg production
[0034] 1 Test materials
[0035] Randomly select 50 Jining Bairi Chickens (Jining Datang Bairi Chicken Conservation Farm), 50 Xinyang Brown Chickens (Shanghai Poultry Breeding Co., Ltd.), 50 Wenshang Reed Chickens (Wenshang County, Jining City, Shandong Province), 45 Hailan brown chickens (Shandong Tai'an Hailan Brown Breeding Company) and 550 recessive Bailuoke chickens with egg laying records (Shandong Jihua Poultry Breeding Co., Ltd.). All of the above were random sampling, blood was collected from the wing vein, and the genome was extracted and stored at -20℃.
[0036] 2 Test method
[0037] 2.1 PCR amplification
[0038] Use the genome as a template to perform PCR amplification. The primers are shown in Table 1. The reaction system is 40μL, including 2μL genomic DNA (50-100ng), 20μL 2×PrimeSTARGCBuffer, 3.2μL dNTPs (2.5mM each, TaKaRa), ups...
Embodiment 3
[0067] Example 3 Effects of polymorphic sites in the 5'regulatory region of chicken PTHLH on gene expression
[0068] 1 Test materials
[0069] Randomly sample healthy Hailan brown chickens (3-5 chickens) in the peak egg production period from the Linxi Village Farm in Tai'an City,
[0070] 2 Test method
[0071] 2.1 Construction of a mutant luciferase expression vector at a polymorphic site in the 5′ regulatory region of PTHLH
[0072] 1) In the recessive Bailock population, select PTHLH 5'regulatory regions at positions-1827 and -165 respectively for wild-type and mutant individuals, and use their DNA as a template to obtain the wt-PTHLH and mut-PTHLH sequences. The length of the amplified fragment is 2144bp, and the primer sequence is the same as Seq ID No. 1 and 2.
[0073] 2) PCR amplification
[0074] The amplification reaction adopts the high-fidelity enzyme PrimeSTAR, and the reaction system (20ul) includes: 2×PrimeSTARGCBuffer 10ul, 1.6μL dNTPs (2.5mM each, TaKaRa), plus 0.5μL (...
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