The invention of DNA from the progeny produced from beef steers groups Sires candidate after separation and purification, located in exon 2 After the two kinds of bovine leptin gene nucleotide sequence of the primer by synthesis of a second locus having a specific nucleotide sequence and PCR performed using a PCR-product 2 kinds of restriction enzymes was reacted with Kpn2 I, Msp I alleles was analyzed in the form of meat quality and relevance to black. Using the frequency of the leptin gene obtained from the PCR-RFLP can identify the characteristics of the beef population. TT genotype of Kpn2 I showed statistical significance in relation to the meat. Using the expression frequency of the genotype by PCR-RFLP analysis to identify the genetic characteristics of the beef, and can obtain a large effect in improving the TT genotype using a molecular marker for beef meat quality improvement.
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机译:分离并纯化来自牛ste公牛组Sires候选物后代的DNA的发明,位于第2外显子上通过合成具有特定核苷酸序列的第二个基因座和引物进行了两种牛瘦素基因的引物核苷酸序列的PCR使用PCR产物,将2种限制酶与Kpn2 I反应,以肉质和与黑度的相关性形式分析了Msp I I>等位基因。使用从PCR-RFLP获得的瘦素基因的频率可以识别牛肉群体的特征。 Kpn2 I的 TT基因型 I>与肉相关,具有统计学意义。通过PCR-RFLP分析利用基因型的表达频率来鉴定牛肉的遗传特性,并且使用用于改善牛肉品质的分子标记,可以在改善TT基因型上获得很大的效果。
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