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首页> 外文期刊>Turkish Journal of Veterinary and Animal Sciences >Determination of the allele frequency of some genomic loci in a holstein cattle population and its importance in individual identification
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Determination of the allele frequency of some genomic loci in a holstein cattle population and its importance in individual identification

机译:荷斯坦牛种群中一些基因组基因座的等位基因频率的确定及其在个体识别中的重要性

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摘要

Nowadays, the use of DNA sequences with genetic techniques and DNA polymorphism as genetic markers is increasing very rapidly. In this study, we examined the frequencies of seven different polymorphic loci in the cattle population of Istanbul University Veterinary Medicine Research and Application Farm (Turkey). Thus, our aim was to examine and calculate the power of exclusion, match probability and power of discrimination of the seven loci, and examine the usefulness of the involved loci in identification tests. For DNA extraction, Chelex and Phenol-Chloroform-Isoamil alcohol methods were applied to the blood taken from animals. After measuring the amount and purity degree of DNA with a spectrophotometer, seven DNA loci were amplified by PCR. Theamplification products were stained with EtBr and examined with 1.5% Agarose gel electrophoresis. Using denaturated polyacrylamide gel electrophoresis and silver staining, PCR products were evaluated and phenotypes of the alleles were determined. At theend of the study, a mismatch to the Hardy-Weinberg equilibrium was observed in all loci but BMS1822. The highest heterozygosity ratio was 83.3% for BMS2270, and the lowest ratio was 31.4% for BMS2721 among the seven STR/microsatellite loci we studied. The highest exclusion probability was 0.662 for BMS 2270, and the lowest was 0.066 for BMS2721. The highest power of discrimination was 0.947 for BMS2270, and the lowest was 0.504 for BMS2721. The highest matching probability was for BMS3019 and BMS2721,and the lowest was for BMS2270 and BMS1822. It was observed that the loci in this study have very high power of discrimination and power of exclusion values when combined. Thus, these systems may be useful as markers in DNA profiling.
机译:如今,利用遗传技术和DNA多态性作为遗传标记的DNA序列的使用正在迅速增加。在这项研究中,我们检查了伊斯坦布尔大学兽医研究与应用农场(土耳其)牛群中七个不同多态性基因座的频率。因此,我们的目的是检查和计算七个位点的排斥力,匹配概率和判别力,并检查参与位点在鉴定测试中的有用性。对于DNA提取,将Chelex和苯酚-氯仿-Isoamil酒精方法应用于动物血液。用分光光度计测量DNA的数量和纯度后,通过PCR扩增了七个DNA基因座。扩增产物用EtBr染色,并用1.5%琼脂糖凝胶电泳检查。使用变性聚丙烯酰胺凝胶电泳和银染,评估PCR产物并确定等位基因的表型。在研究结束时,在除BMS1822之外的所有基因座中均观察到与Hardy-Weinberg平衡不匹配。在我们研究的七个STR /微卫星基因座中,BMS2270的最高杂合率为83.3%,而BMS2721的最低杂合率为31.4%。 BMS 2270的最高排除概率为0.662,而BMS2721的最低排除概率为0.066。 BMS2270的最高鉴别力为0.947,而BMS2721的最低鉴别力为0.504。匹配概率最高的是BMS3019和BMS2721,最低的是BMS2270和BMS1822。观察到,当组合时,该研究中的基因座具有很高的判别力和排除值的能力。因此,这些系统可用作DNA谱分析中的标记。

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