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首页> 外文期刊>The Journal of Veterinary Medical Science >Development of Allele-Specific Primer PCR for a Swine TLR2 SNP and Comparison of the Frequency among Several Pig Breeds of Japan and the Czech Republic
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Development of Allele-Specific Primer PCR for a Swine TLR2 SNP and Comparison of the Frequency among Several Pig Breeds of Japan and the Czech Republic

机译:猪TLR2 SNP等等位基因特异性引物PCR的开发,以及日本几种猪品种和捷克共和国频率的比较

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References(22) Cited-By(2) In the present study, we have developed an allele-specific primer-polymerase chain reaction (ASP-PCR) for genotyping a single nucleotide polymorphism (SNP) of swine Toll-like receptor 2 (TLR2) (C406G), which is related to the prevalence of pneumonia caused by Mycoplasma hyopneumoniae. We also compared the allele frequency among several pig breeds of Japan and the Czech Republic. Allele-specific primers were constructed by introducing 1-base mismatch sequence before the SNP site. The swine TLR2 C406G mutation was successfully determined by the ASP-PCR using genomic DNA samples in Japan as previously genotyped by a sequencing method. Using the PCR condition determined, genomic DNA samples from pig blood obtained from 110 pigs from 7 different breeds in the Czech Republic were genotyped by the ASP-PCR. The genotyping results from the ASP-PCR were completely matched with the results from the sequencing method. The allele frequency of the swine TLR2 C406G mutation was 27.5% in the Czech Republic and 3.6% in Japan. The C406G mutation was only found in the Landrace breed in Japan, and was almost exclusively found in the Landrace breed in the Czech Republic as well. These results indicated the usefulness of ASP-PCR for detecting a specific SNP for swine TLR2.
机译:参考(22)引用(2)在本研究中,我们开发了一种等位基因特异性引物聚合酶链反应(ASP-PCR),用于基因分型为猪沟状受体2的单个核苷酸多态性(SNP)(TLR2 )(C406G),与肺炎肺炎植物引起的肺炎引起的患病率有关。我们还将等位基因频率与日本和捷克共和国的几种猪品种之间进行了比较。通过在SNP位点之前引入1-碱基错配序列来构建等位基因特异性引物。猪TLR2C406G突变通过ASP-PCR使用日本的基因组DNA样品成功确定,如先前通过测序方法的基因分型。使用所确定的PCR病症,由捷克共和国7种不同品种的110只猪获得的猪血液的基因组DNA样品被ASP-PCR基因分型。 ASP-PCR的基因分型结果与测序方法的结果完全匹配。捷克共和国的猪TLR2 C406G突变的等位基因频率为27.5%,日本3.6%。 C406G突变仅在日本的Landrace品种中发现,并且在捷克共和国的兰德斯品种中几乎完全被发现。这些结果表明了ASP-PCR用于检测猪TLR2的特定SNP的有用性。

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