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首页> 外文期刊>Acta Biochimica Polonica >Analysis of Slovak Spotted breed for bovine beta casein A1 variant as risk factor for human health*
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Analysis of Slovak Spotted breed for bovine beta casein A1 variant as risk factor for human health*

机译:斯洛伐克斑病牛β酪蛋白A1变异作为人类健康的危险因素分析*

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摘要

The goal of work was identification A1 variant of bovine beta casein which involves ischemic heart disease and diabetes mellitus in human. The digestion of A1beta casein can result in the production of bioactive beta casomorphin-7 (BCM-7); this is not the case with A2. This bioactive peptide has been linked to physiological traits that may elicit effects on components of the vascular and immune systems. The material involved 111 Slovak Spotted breed. Bovine genomic DNA was extracted from whole blood by using commercial kit, and used in order to estimate beta-casein genotypes by means of PCRRFLP method. The PCR products were digested with DdeI restriction enzyme. In the population included in the study were detected all three genotypes, homozygote genotype A1A1 (14 animals), heterozygote genotype A1A2 (37 animals) and homozygote genotype A2A2 (60 animals). In the total population of cattle homozygotes A2A2–0.5405 were the most frequent, while homozygotes A1A1–0.1261 were the least frequent ones. This suggests a superiority of allele A2 (0.7072) which does not produce BCM-7, and thus is safe for human consumption. The expected homozygosity for gene CSN2 is in the population stated a slight increase in homozygosity (0.5858). This caused a slight decrease in the level of possible variability realization (41.80%), which corresponds to the effective number of alleles (1.7071).
机译:工作的目标是鉴定牛β酪蛋白的A1变异体,该变异体涉及人体的缺血性心脏病和糖尿病。 A1beta酪蛋白的消化可导致产生生物活性的βcasomorphin-7(BCM-7); A2并非如此。这种生物活性肽已与可能引起对血管和免疫系统成分的影响的生理特性相关联。该材料涉及111个斯洛伐克斑点犬种。使用商业试剂盒从全血中提取牛基因组DNA,并用于通过PCRRFLP方法估计β-酪蛋白基因型。 PCR产物用DdeI限制酶消化。在研究的人群中,检测到所有三种基因型,纯合子基因型A1A1(14只动物),杂合子基因型A1A2(37只动物)和纯合子基因型A2A2(60只动物)。在牛的总种群中,纯合子A2A2–0.5405最频繁,而纯合子A1A1–0.1261最不频繁。这暗示了不产生BCM-7的等位基因A2(0.7072)的优越性,因此对于人类食用是安全的。基因CSN2的预期纯合性在人群中表明纯合性略有增加(0.5858)。这导致可能的可变性实现水平略有下降(41.80%),与等位基因的有效数量(1.7071)相对应。

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