首页> 外文期刊>Meat Science >Differentiation of European wild boar (Sus scrofa scrofa) and domestic swine (Sus scrofa domestica) meats by PCR analysis targeting the mitochondrial D-loop and the nuclear melanocortin receptor 1 (MC1R) genes
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Differentiation of European wild boar (Sus scrofa scrofa) and domestic swine (Sus scrofa domestica) meats by PCR analysis targeting the mitochondrial D-loop and the nuclear melanocortin receptor 1 (MC1R) genes

机译:通过靶向线粒体D环和核黑素皮质素受体1(MC1R)基因的PCR分析,区分欧洲野猪(Ss scrofa scrofa)和家养猪(Ss scrofa domestica)肉

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This work describes the differentiation of European wild boar (Sus scrofa scrofa) and domestic swine (Sus scrofa domestica) meats by PCR targeting sequences from two molecular markers: the mitochondrial displacement loop (D-loop) region and the nuclear melanocortin receptor 1 (MC1R) gene. A polymorphic D-loop fragment (~270 bp) was amplified and sequenced in a number of wild and domestic Sus scrofa meat samples, to find a nucleotide region suitable for PCR-RFLP analysis. Sequence data showed the presence of only a few point mutations across Sus scrofa D-loop sequences, not allowing direct discrimination between wild boar and domestic swine meats. Later, the MC1R gene was targeted and Sus wrofa-specific primers designed to amplify a 795 bp MC1R fragment. Subsequent RFLP analysis of the MC1R swine-specific amplicons allowed selection of BspHI and BstUI endonucleases to carry out intraspecific Sus scrofa differentiation. Digestion of MC1R amplicons with the chosen enzymes generated characteristic PCR-RFLP profiles that allowed discrimination among meats from wild and domestic swine specimens. The technique also enabled the detection of samples that yielded heterozygous profiles, suggesting hybrids resulting from wild boar and domestic pig breeding. The PCR-RFLP reported here, targeting the MC1R gene may be routinely applied to verify the correct labelling of game products.
机译:这项工作描述了通过两种分子标记的PCR靶向序列对欧洲野猪(Ss scrofa scrofa)和家养猪(Ss scrofa domestica)肉的区分:线粒体置换环(D-loop)区和黑素皮质素受体1(MC1R) )基因。扩增了一个多态性的D-loop片段(〜270 bp),并在许多野生和家养的野猪肉样品中测序,以找到适合PCR-RFLP分析的核苷酸区域。序列数据显示,整个Sus scrofa D环序列仅存在一些点突变,无法直接区分野猪和家养猪肉。后来,以MC1R基因为靶标,并设计了Sus wrofa特异性引物来扩增795 bp MC1R片段。随后的MC1R猪特异性扩增子的RFLP分析允许选择BspHI和BstUI核酸内切酶来进行种内Sus scrofa分化。用选定的酶消化MC1R扩增子可产生特征性PCR-RFLP图谱,从而可区分野生和家养猪标本中的肉。该技术还能够检测产生杂合子谱的样品,这表明由野猪和家猪育种产生的杂种。此处报道的靶向MC1R基因的PCR-RFLP可以常规应用于验证游戏产品的正确标记。

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