Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan; Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.
Gene. 2014 Sep 15;548(2):217-22. doi: 10.1016/j.gene.2014.07.035. Epub 2014 Jul 15.
Short Tandem Repeat (STR) genetic markers hold great potential in forensic investigations, molecular diagnostics and molecular genetics research. AmpFlSTR® Identifiler™ PCR amplification kit is a multiplex system for co-amplification of 15 STR markers used worldwide in forensic investigations. This study attempts to assess forensic validity of these STRs in Pakistani population and to investigate its applicability in quick and simultaneous diagnosis and tracing parental source of common chromosomal aneuploidies.
Samples from 554 healthy Pakistani individuals from 5 different ethnicities were analyzed for forensic parameters using Identifiler STRs and 74 patients' samples with different aneuploidies were evaluated for diagnostic strengths of these markers.
All STRs hold sufficient forensic applicability in Pakistani population with paternity index between 1.5 and 3.5, polymorphic information content from 0.63 to 0.87 and discrimination power ≥0.9 (except TPOX locus). Variation from Hardy-Weinberg equilibrium was observed at some loci reflecting selective breeding and intermarriages trend in Pakistan. Among aneuploidic samples, all trisomies were precisely detectable while aneuploidies involving sex chromosomes or missing chromosomes were not clearly detectable using Identifiler STRs. Parental origin of aneuploidy was traceable in 92.54% patients.
The studied STR markers are valuable tools for forensic application in Pakistan and utilizable for quick and simultaneous identification of some common trisomic conditions. Adding more sex chromosome specific STR markers can immensely increase the diagnostic and forensic potential of this system.
短串联重复(STR)遗传标记在法医学调查、分子诊断和分子遗传学研究中具有巨大潜力。AmpFlSTR®Identifiler™PCR 扩增试剂盒是一种用于共扩增 15 个 STR 标记的多重系统,在全球法医学调查中得到广泛应用。本研究试图评估这些 STR 在巴基斯坦人群中的法医学有效性,并研究其在快速和同时诊断和追踪常见染色体非整倍体的父母来源中的适用性。
对来自 5 个不同民族的 554 名健康巴基斯坦个体的样本进行了Identifiler STR 分析,对 74 名具有不同非整倍体的患者样本进行了这些标记物的诊断强度评估。
所有 STR 在巴基斯坦人群中均具有足够的法医学适用性,亲权指数在 1.5 至 3.5 之间,多态信息含量在 0.63 至 0.87 之间,鉴别力≥0.9(除 TPOX 基因座外)。一些基因座偏离哈迪-温伯格平衡,反映了巴基斯坦选择性繁殖和通婚的趋势。在非整倍体样本中,所有三体均能准确检测到,而涉及性染色体或缺失染色体的非整倍体则不能用 Identifiler STR 清晰检测到。在 92.54%的患者中可追踪到非整倍体的父母来源。
研究的 STR 标记是巴基斯坦法医学应用的有价值工具,可用于快速和同时鉴定一些常见的三体条件。添加更多的性染色体特异性 STR 标记可以极大地增加该系统的诊断和法医学潜力。