首页> 外国专利> A method for the diagnosis of polymorphism of the NHLRC2 gene, causing a genetic defect in the duplication of the development of cattle of Aberdeen-Angus breed

A method for the diagnosis of polymorphism of the NHLRC2 gene, causing a genetic defect in the duplication of the development of cattle of Aberdeen-Angus breed

机译:一种诊断NHLRC2基因多态性的方法,该基因在阿伯丁-安格斯牛的发育重复中引起遗传缺陷

摘要

FIELD: biotechnology.SUBSTANCE: invention relates to biotechnology, in particular to methods for determining polymorphism of a gene associated with an undesirable recessive genetic duplication defect characteristic of cattle Aberdeen-Angus breed, specifically the NHLRC2 gene associated with the DDC haplotype. Method involves analysis of DNA extracted from biomaterial of animals by PCR method, characterized by that oligonucleotide primers of 20 bp are used for amplification of DNA fragment of mutation area. with melting point 59 °C and content of guanine-cytosine 55 %, forming in PCR amplicon length of 404 base pairs, which is then subjected to RFLP-analysis using enzyme BstMW I (restriction endonuclease) with recognition site GCNNNNN↑NNGC (CGNN↓NNNNNCG), which cuts out the PCR product in case of mutation on two DNA fragments - 320 base pairs and 84 base pairs.EFFECT: method is applicable in the farm animals genetics for detecting polymorphism in the Aberdeen-Angus cattle NHLRC2 gene associated with the genetic duplication defect (DD) carrier haplotype, in order to further use of obtained results in breeding and selection of cattle in breeding and commodity farms of meat cattle breeding industry.1 cl, 1 dwg, 1 ex
机译:技术领域本发明涉及生物技术,尤其是用于确定与牛阿伯丁-安格斯牛的不良隐性遗传重复缺陷特征相关的基因,特别是与DDC单倍型相关的NHLRC2基因的多态性的方法。该方法涉及通过PCR方法分析从动物生物材料中提取的DNA,其特征在于使用20bp的寡核苷酸引物扩增突变区域的DNA片段。熔点为59°C,鸟嘌呤-胞嘧啶含量为55%,在PCR扩增子长度中形成404个碱基对,然后使用带有识别位点GCNNNNN↑NNGC(CGNN↓)的BstMW I(限制性内切核酸酶)酶进行RFLP分析NNNNNCG),可在两个DNA片段发生突变的情况下切下PCR产物-320个碱基对和84个碱基对。效果:该方法适用于农场动物遗传学,以检测与Aberdeen-Angus牛NHLRC2基因相关的多态性遗传重复缺陷(DD)携带者单倍型,以便进一步将获得的结果用于肉牛育种业的育种和商品农场的牛育种和选择中.1 cl,1 dwg,1 ex

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