Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, PO Box 23, Vojvode Stepe 444a, Belgrade, 11010, Serbia.
Department of Genetics of Populations and Ecogenotoxicology, Institute for Biological Research "Siniša Stanković", National Institute of Republic of Serbia, University of Belgrade, Bulevar despota Stefana 142, Belgrade, 11060, Serbia.
Int J Legal Med. 2020 Sep;134(5):1581-1590. doi: 10.1007/s00414-020-02324-x. Epub 2020 Jun 6.
Mitochondrial genome (mtDNA) is a valuable resource in resolving various human forensic casework. The usage of variability of complete mtDNA genomes increases their discriminatory power to the maximum and enables ultimate resolution of distinct maternal lineages. However, their wider employment in forensic casework is nowadays limited by the lack of appropriate reference database. In order to fill in the gap in the reference data, which, considering Slavic-speaking populations, currently comprises only mitogenomes of East and West Slavs, we present mitogenome data for 226 Serbians, representatives of South Slavs from the Balkan Peninsula. We found 143 (sub)haplogroups among which West Eurasian ones were dominant. The percentage of unique haplotypes was 85%, and the random match probability was as low as 0.53%. We support previous findings on both high levels of genetic diversity in the Serbian population and patterns of genetic differentiation among this and ten studied European populations. However, our high-resolution data supported more pronounced genetic differentiation among Serbians and two Slavic populations (Russians and Poles) as well as expansion of the Serbian population after the Last Glacial Maximum and during the Migration period (fourth to ninth century A.D.), as inferred from the Bayesian skyline analysis. Phylogenetic analysis of haplotypes found in Serbians contributed towards the improvement of the worldwide mtDNA phylogeny, which is essential for the interpretation of the mtDNA casework.
线粒体基因组(mtDNA)是解决各种人类法医学案件的宝贵资源。利用完整 mtDNA 基因组的变异性可以最大限度地提高其鉴别力,并能够最终解决不同的母系谱系。然而,由于缺乏适当的参考数据库,它们在法医案件中的更广泛应用目前受到限制。为了填补参考数据的空白,考虑到斯拉夫语人群,目前仅包括东斯拉夫人和西斯拉夫人的线粒体基因组,我们提供了来自巴尔干半岛的南斯拉夫人 226 名塞尔维亚人的线粒体基因组数据。我们在其中发现了 143 个(亚)单倍群,其中西欧亚单倍群占主导地位。独特单倍型的百分比为 85%,随机匹配概率低至 0.53%。我们支持先前关于塞尔维亚人群遗传多样性水平高以及该人群与十个研究的欧洲人群之间遗传分化模式的发现。然而,我们的高分辨率数据支持塞尔维亚人和两个斯拉夫人群(俄罗斯人和波兰人)之间更明显的遗传分化,以及贝叶斯天际线分析推断的末次冰期最大值和迁徙时期(公元四至九世纪)后塞尔维亚人口的扩张。在塞尔维亚人中发现的单倍型的系统发育分析有助于改进全球范围内的 mtDNA 系统发育,这对于 mtDNA 案件的解释至关重要。