UCP3 gene and molecular marker related to pig intramuscular fat character, and application of UCP3 gene and molecular marker
An intramuscular fat and molecular marker technology, which can be used in applications, genetic engineering, plant genetic improvement, etc., and can solve problems such as unclearness
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Embodiment 1
[0045] Embodiment 1: Clone the full-length cDNA clone of porcine UCP3 gene
[0046] 1.1. Primer design
[0047] Take the NCBI database ( https: / / www.ncbi.nlm.nih.gov / ) The predicted porcine UCP3 gene mRNA sequence (NM_214049.1) seed sequence is used as a template to design amplification primers, wherein the 5'-RACE specific primers (GSPs) should satisfy the length of 23-28nt and the GC content of 50-70% between, and Universal Primer Mix ( The general primers designed by the RACE5' / 3'Kit kit have the conditions that the 3' end of Long Primer and Short Primer are not complementary, etc., and two primers that meet the above conditions are designed, namely GSP1 and NGSP1. GATTACGCCAAGCTT was added at the 'end to facilitate vector ligation and sequencing in subsequent experiments. The design of UCP3 gene 3'-RACE-specific primers was similar to that of 5'-RACE-specific primers. The designed primers were named GSP2 and NGSP2 respectively, and GATTACGCCAAGCTT was still added to ...
Embodiment 2
[0055] Example 2: Analysis of pig UCP3 gene expression pattern
[0056]In order to determine the relationship between UCP3 expression pattern and fat deposition in pigs, the present invention randomly selected 3 Duroc×Meishan pig binary hybrid pigs, and collected heart, liver, lung, spleen, kidney, fat, and biceps femoris, At the same time, the skeletal muscle tissues of biceps femoris (fast muscle, white muscle) and soleus muscle (slow muscle, red muscle) of different muscle fiber types were collected from 5 experimental pigs. Utilize TRIzol reagent to carry out the extraction of total RNA (Invitrogen company product), utilize Prime Script TM Reagents were used to synthesize the first strand of cDNA (products of TaKaRa Company). Then Real-time PCR was used to detect the mRNA expression level of UCP3 gene. Based on the cloned porcine UCP3 gene full-length cDNA nucleotide sequence SEQ ID NO: 1 as a reference, real-time PCR quantitative primers were designed. The quantitative ...
Embodiment 3
[0058] Example 3: Detection of genetic variation sites of pig UCP3 gene and identification of intramuscular fat-related molecular markers
[0059] 2.1. Experimental pigs and trait determination
[0060] The 279 (skin × du) × (length × large) quaternary commercial pigs involved in the present invention, the measured traits include carcass weight, backfat thickness, pH 45min , pH 24h , L* 45min 、a* 45min 、b* 45min , L* 24h 、a* 24h 、b* 24h , drip loss 24h , drip loss 48h , glycogen content, glucose content, glucose-6 phosphate content, lactic acid content, glycolytic potential, cooking loss, shear force. Finally, the rib backfat thickness was measured with an electronic vernier caliper, the pH value was measured with a portable pH meter (model: HI9125portable pH, Australia), the cooking loss was calculated using the loss rate after boiling for 10 minutes, and the shear force was measured with a domestic instrument. Meat color L*, a *, b* were measured with a portable co...
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