Zupanic Pajnic I, Balazic J, Komel R
Institute of Forensic Medicine, Faculty of Medicine, Korytkova 2, 1000 Ljubljana, Slovenia.
Int J Legal Med. 2004 Feb;118(1):1-4. doi: 10.1007/s00414-003-0394-3. Epub 2003 Oct 8.
The forensic application of mitochondrial DNA (mtDNA) typing requires large and regionally well-defined databases. To expand the database for forensic identification purposes in Slovenia, the mtDNA control region sequences of the hypervariable regions HVI and HVII were determined in a population of 129 maternally unrelated Slovenians, using a fluorescent-based capillary electrophoresis sequencing method. A total of 111 different haplotypes resulting from 124 polymorphic positions (80 polymorphic positions in HVI and 44 in HVII) were found. Of these, 101 mtDNA types were unique, 6 haplotypes were shared by 2 individuals, 1 haplotype by 3 individuals, 2 haplotypes by 4 individuals, and the most common haplotype was found in 5 individuals. The most frequent haplotypes in the Slovenian population,263(G), 315.1(C) and 263(G), 309.1(C), 315.1(C) are also the most common in other European populations. The data support the concept that these haplotypes may represent a common European mtDNA sequence types. The sequence poymorphisms were compared to the databases of west Austria and central Italy and the HVI and HVII sequence matching probabilities within and between populations were calculated. It is 1.1-4.5 times more likely to find a sequence match in a random pair of Slovenians than in a random Slovenian-Italian pair and in a random Slovenian-Austrian pair. The length heteroplasmy in the homopolymeric C-stretch regions located at nucleotide positions 16184-16193 in HVI and at positions 303-315 in HVII was observed in 17% and 8% of individuals, respectively. A statistical estimate of the results for this population showed the random match probability and the genetic diversity of 1.16% and 0.996, respectively.
线粒体DNA(mtDNA)分型的法医应用需要大型且地域界定明确的数据库。为了扩大斯洛文尼亚用于法医鉴定目的的数据库,采用基于荧光的毛细管电泳测序方法,对129名母系无关的斯洛文尼亚人的线粒体DNA控制区高变区HVI和HVII的序列进行了测定。共发现了124个多态性位点(HVI中有80个多态性位点,HVII中有44个)产生的111种不同单倍型。其中,101种mtDNA类型是独特的,6种单倍型由2个人共享,1种单倍型由3个人共享,2种单倍型由4个人共享,最常见的单倍型在5个人中被发现。斯洛文尼亚人群中最常见的单倍型263(G)、315.1(C)以及263(G)、309.1(C)、315.1(C)在其他欧洲人群中也最为常见。这些数据支持了这些单倍型可能代表常见欧洲mtDNA序列类型的概念。将序列多态性与奥地利西部和意大利中部的数据库进行了比较,并计算了群体内部和群体之间HVI和HVII序列匹配概率。在随机配对的斯洛文尼亚人之间找到序列匹配的可能性比在随机配对的斯洛文尼亚人与意大利人之间以及随机配对的斯洛文尼亚人与奥地利人之间高1.1至4.5倍。分别在17%和8%的个体中观察到HVI中位于核苷酸位置16184 - 16193的同聚物C延伸区域以及HVII中位于位置303 - 315的长度异质性。对该群体结果的统计估计显示,随机匹配概率和遗传多样性分别为1.16%和0.996。