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运用聚合酶链式反应(PCR)及两种电泳形式对STR基因座HUMTH01进行研究:英国和加利西亚白种人群体调查及其在亲子鉴定中的应用价值。

Investigation of the STR locus HUMTH01 using PCR and two electrophoresis formats: UK and Galician Caucasian population surveys and usefulness in paternity investigations.

作者信息

Lareu M V, Phillips C P, Carracedo A, Lincoln P J, Syndercombe Court D, Thomson J A

机构信息

Department of Legal Medicine, University of Santiago de Compostela, Spain.

出版信息

Forensic Sci Int. 1994 May 25;66(1):41-52. doi: 10.1016/0379-0738(94)90318-2.

Abstract

Two hundred unrelated Caucasians from the UK and 210 from Galicia (NW Spain) have been genotyped for the HUMTH01 locus using polymerase chain reaction (PCR) amplification followed by high sieving agarose electrophoresis (UK samples) and polyacrylamide electrophoresis (Galician samples). Allele and genotype frequencies obtained from both populations were in close agreement to those seen by other workers and chi 2 tests of the two populations showed that both were in Hardy-Weinberg equilibrium. The potential usefulness of HUMTH01 in paternity investigations was analysed by constructing, within each population, false family trios, each with a non-father, in order to estimate the actual exclusion rate. The observed rate of exclusion was in close agreement with the expected rate for both populations. Examination of the mother-child pairs in the false families showed a common allele in every case and no evidence of mutation or non-Mendelian inheritance was observed. The HUMTH01 locus shows an informative polymorphism and the production and analysis of population databases is easily achieved. The use of PCR followed by electrophoresis in either gel format appears to provide a quick and straightforward method for investigating the HUMTH01 locus.

摘要

对来自英国的200名无亲缘关系的白种人和来自加利西亚(西班牙西北部)的210名白种人,使用聚合酶链反应(PCR)扩增,随后分别采用高分辨率琼脂糖电泳(英国样本)和聚丙烯酰胺电泳(加利西亚样本),对HUMTH01基因座进行基因分型。从这两个人群获得的等位基因和基因型频率与其他研究人员观察到的结果非常一致,并且对这两个人群进行的卡方检验表明,两者均处于哈迪-温伯格平衡状态。通过在每个人群中构建包含一名非父亲的虚假三联体家庭,来分析HUMTH01在亲子鉴定调查中的潜在用途,以便估计实际排除率。两个群体的观察到的排除率与预期率非常一致。对虚假家庭中的母子对进行检查,发现每个案例中都有一个共同的等位基因,并且未观察到突变或非孟德尔遗传的证据。HUMTH01基因座显示出信息丰富的多态性,并且很容易建立和分析群体数据库。采用PCR随后进行凝胶电泳似乎为研究HUMTH01基因座提供了一种快速且直接的方法。

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