Zemskova E Iu, Frolova S A, Sleptsova Zh V, Ivanov P L
Sud Med Ekspert. 2003 Jul-Aug;46(4):19-22.
The properties of amelogenin amplification system and, in particular, of its species specificity, were studied. DNA preparations extracted from cattle (cow/bull), pig, ram and from poultry (hen), as well as from dog and cat, were used as a matrix for polymerase chain reaction (PCR) involving a standard scheme of enzymatic amplification of the amelogenin gene. It was demonstrated that, unlike for the human DNA, the amelogenin test couldn't be used for the DNA of examined animals as a sex-specific marker. However, there is a danger of a false determination of the male sex in the female origin samples during a forensic-experts' typing of the amelogenin gene, if there is an admixture of an animal DNA to a human DNA preparation. As for the biological samples of the animal origin, there is a possibility of a false-female sex determination. It can be attributed to an incorrectly selected standard of the molecular weight or to its remote location on the gel as well as to the use of an inaccurately calculated algorithm designed for determining the sizes of analyzed fragments.
对牙釉蛋白扩增系统的特性,尤其是其物种特异性进行了研究。从牛(母牛/公牛)、猪、羊以及家禽(母鸡),还有狗和猫身上提取的DNA制剂,被用作聚合酶链反应(PCR)的模板,该反应涉及牙釉蛋白基因的标准酶促扩增方案。结果表明,与人类DNA不同,牙釉蛋白检测不能用作被检测动物DNA的性别特异性标记。然而,在法医专家对牙釉蛋白基因进行分型时,如果人类DNA制剂中混有动物DNA,那么在女性来源样本中存在误判为男性性别的风险。至于动物来源的生物样本,则存在误判为女性性别的可能性。这可能归因于分子量标准选择不当、其在凝胶上的位置偏远,以及使用了为确定分析片段大小而设计的计算不准确的算法。