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从法医降解骨DNA进行性别鉴定的难点:三种方法的比较

Difficulties of sex determination from forensic bone degraded DNA: A comparison of three methods.

作者信息

Quincey Danielle, Carle Georges, Alunni Véronique, Quatrehomme Gérald

机构信息

Faculté de Médecine, Université de Nice Sophia Antipolis, Nice cedex 2, France.

出版信息

Sci Justice. 2013 Sep;53(3):253-60. doi: 10.1016/j.scijus.2013.04.003. Epub 2013 May 1.

Abstract

Sex determination is of paramount importance in forensic anthropology. Numerous anthropological methods have been described, including visual assessments and various measurements of bones. Nevertheless, whatever the method used, the percentage of correct classification of a single bone usually varies between 80% and 95%, due to significant intra- and inter-population variations, and sometimes variations coming from secular trends. DNA is increasingly used in a forensic context. But forensic DNA extraction from bone raises several issues, because the samples are very often badly altered and/or in very small quantity. Nuclear DNA is difficult to get from degraded samples, according to low copy number, at least in comparison with mitochondrial DNA. In a forensic context (as in a paeleoanthropological context) DNA sex determination is usually complicated by the weak amount of DNA, the degraded nature of nucleic acids, the presence of enzymatic inhibitors in DNA extracts, the possible faint amplification of Y band and the risk of contamination during either excavation or manipulation of samples. The aim of this work was to compare three methods of DNA sex determination from bones: procedure #1 using a single PCR amplification, procedure #2 using a double PCR amplification, and procedure #3 adding bleaching for decontamination of the bone, instead of simply rubbing the bone. These processes were applied to samples of bones (49 samples coming from 39 individuals) that were in various states of post mortem alteration. The main results are the following. (i) No DNA could be extracted from three skulls (parietal bones, mastoid process), the compact bone of one rib, and the diaphysis of one femur; (ii) there was a contamination in three skulls; and (iii) the Y band did not appear in two male cases, with one of the three procedures (male tibia, procedure #2) and with procedures #2 and #3 (male femur). This study emphasises the main issue while working with altered bones: the impossibility to extract DNA in some cases, and, worth of all, the contamination of the sample or the faint amplification of Y band which leads to a wrong sex answer. Multiple and significant precautions have to be taken to avoid such difficulties.

摘要

性别鉴定在法医人类学中至关重要。人们已经描述了许多人类学方法,包括视觉评估和对骨骼的各种测量。然而,无论使用何种方法,由于人群内部和人群之间存在显著差异,有时还存在长期趋势导致的差异,单块骨骼正确分类的百分比通常在80%至95%之间。DNA在法医领域的应用越来越广泛。但是从骨骼中提取法医DNA会引发几个问题,因为样本常常严重降解和/或数量极少。与线粒体DNA相比,至少就低拷贝数而言,从降解样本中很难获得核DNA。在法医环境中(如同在古人类学环境中),DNA性别鉴定通常因DNA量少、核酸降解、DNA提取物中存在酶抑制剂、Y带可能微弱扩增以及样本挖掘或处理过程中存在污染风险而变得复杂。这项工作的目的是比较三种从骨骼中进行DNA性别鉴定的方法:方法1使用单一PCR扩增,方法2使用双重PCR扩增,方法3添加漂白剂对骨骼进行去污处理,而不是简单地擦拭骨骼。这些方法应用于处于不同死后改变状态的骨骼样本(来自39个人的49个样本)。主要结果如下。(i)从三个头骨(顶骨、乳突)、一根肋骨的密质骨和一根股骨的骨干中无法提取到DNA;(ii)三个头骨存在污染;(iii)在两例男性样本中,使用三种方法之一(男性胫骨,方法2)以及使用方法2和方法3(男性股骨)时,Y带未出现。这项研究强调了处理受损骨骼时的主要问题:在某些情况下无法提取DNA,最重要的是,样本污染或Y带微弱扩增会导致错误的性别判定。必须采取多项重要预防措施以避免此类困难。

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