Andréasson Hanna, Allen Marie
Department of Genetics and Pathology, Uppsala University, Rudbeck Laboratory, S-751 85 Uppsala, Sweden.
J Forensic Sci. 2003 Nov;48(6):1280-7.
DNA quantification of forensic evidence is very valuable for an optimal use of the available biological material. Moreover, sex determination is of great importance as additional information in criminal investigations as well as in identification of missing persons, no suspect cases, and ancient DNA studies. While routine forensic DNA analysis based on short tandem repeat markers includes a marker for sex determination, analysis of samples containing scarce amounts of DNA is often based on mitochondrial DNA, and sex determination is not performed. In order to allow quantification and simultaneous sex determination on minute amounts of DNA, an assay based on real-time PCR analysis of a marker within the human amelogenin gene has been developed. The sex determination is based on melting curve analysis, while an externally standardized kinetic analysis allows quantification of the nuclear DNA copy number in the sample. This real-time DNA quantification assay has proven to be highly sensitive, enabling quantification of single DNA copies. Although certain limitations were apparent, the system is a rapid, cost-effective, and flexible assay for analysis of forensic casework samples.
对法医证据进行DNA定量分析,对于优化利用现有的生物材料非常有价值。此外,性别鉴定作为刑事调查以及失踪人员身份确认、无嫌疑人案件和古DNA研究中的附加信息,具有重要意义。虽然基于短串联重复序列标记的常规法医DNA分析包含一个性别鉴定标记,但对含有少量DNA的样本进行分析时,通常基于线粒体DNA,并不进行性别鉴定。为了能够对微量DNA进行定量分析并同时进行性别鉴定,已开发出一种基于对人类牙釉蛋白基因内一个标记进行实时PCR分析的检测方法。性别鉴定基于熔解曲线分析,而外部标准化动力学分析则可对样本中的核DNA拷贝数进行定量。这种实时DNA定量检测方法已被证明具有高度敏感性,能够对单个DNA拷贝进行定量。尽管存在一些明显的局限性,但该系统对于法医案件样本分析而言,是一种快速、经济高效且灵活的检测方法。