Forensic Science Centre "Ivan Vučetić", Ilica 335, 10000 Zagreb, Croatia; Forensic Science Office, University of Zagreb, Ulica Ivana Lučića 5-6, 10000 Zagreb, Croatia.
Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia.
Forensic Sci Int Genet. 2018 May;34:249-256. doi: 10.1016/j.fsigen.2018.03.004. Epub 2018 Mar 9.
In order to implement X-chromosome short tandem repeat (X-STR) typing into routine forensic practice, reference database of a given population should be established. Therefore we extended already published data with additional 397 blood samples from unrelated Croatian citizens, and analyzed the total of 995 samples (549 male and 446 female) typed by Investigator Argus X-12 Kit. To test genetic homogeneity of consecutively processed five historic-cultural regions covering the entire national territory, we calculated pairwise Fst genetic distances between regions based on allele and full haplotype frequencies. Since the comparison did not yield any statistically significant difference, we integrated STR profile information from all regions and used the whole data set to calculate forensic parameters. The most informative marker is DXS10135 (polymorphism information content (PIC = 0.929) and the most informative linkage group (LG) is LG1 (PIC = 0.996). We confirmed linkage disequilibrium (LD) for seven marker pairs belonging to LG2, LG3 and LG4. By including LD information, we calculated cumulative power of discrimination that amounted to 0.999999999997 in females and 0.999999005 in males. We also compared Croatia with 13 European populations based on haplotype frequencies and detected no statistically significant Fst values after Bonferroni correction in any LG. Multi-dimensional scaling plot revealed tight grouping of four Croatian regions amongst populations of southern, central and northern Europe, with the exception of northern Croatia. In this study we gave the first extensive overview of aberrant profiles encountered during Investigator Argus X-12 typing. We found ten profiles consistent with single locus duplication followed by tetranucleotide tract length polymorphism. Locus DXS10079 is by far the most frequently affected one, presumably mutated in eight samples. We also found four profiles consistent with X-chromosome aneuploidy (three profiles with XXX pattern and one profile with XXY pattern). In conclusion, we established integral forensic Croatian X-chromosome database, proved forensic pertinence of Investigator Argus X-12 Kit for the entire Croatian population and identified locus DXS10079 as a potential duplication hotspot.
为了将 X 染色体短串联重复序列(X-STR)分型纳入常规法医实践,应建立特定人群的参考数据库。因此,我们在已发表的数据中扩展了另外 397 个来自克罗地亚无关公民的血样,并分析了 Investigator Argus X-12 试剂盒对总共 995 个样本(549 名男性和 446 名女性)的分型结果。为了检验连续处理的五个历史文化区域的遗传同质性,我们根据等位基因和完整单倍型频率计算了区域之间的成对 Fst 遗传距离。由于比较没有产生任何统计学上显著的差异,我们整合了所有区域的 STR 谱信息,并使用整个数据集计算了法医参数。最具信息量的标记是 DXS10135(多态信息量(PIC)=0.929),最具信息量的连锁群(LG)是 LG1(PIC=0.996)。我们证实了属于 LG2、LG3 和 LG4 的七个标记对之间的连锁不平衡(LD)。通过包括 LD 信息,我们计算出的女性累积鉴别力达到 0.999999999997,男性为 0.999999005。我们还根据单倍型频率将克罗地亚与 13 个欧洲群体进行了比较,在任何 LG 中均未检测到经过 Bonferroni 校正后的统计学显著 Fst 值。多维尺度分析图显示,克罗地亚的四个地区与南欧、中欧和北欧的人群紧密分组,除了北部克罗地亚。在这项研究中,我们首次全面概述了 Investigator Argus X-12 分型过程中遇到的异常谱。我们发现了十个与单个基因座重复后四核苷酸重复长度多态性一致的谱。迄今为止,DXS10079 是受影响最频繁的基因座,可能在八个样本中发生了突变。我们还发现了四个与 X 染色体非整倍体一致的谱(三个 XXX 模式的谱和一个 XXY 模式的谱)。总之,我们建立了完整的克罗地亚 X 染色体法医数据库,证明了 Investigator Argus X-12 试剂盒对整个克罗地亚人口的法医相关性,并确定了 DXS10079 作为潜在的重复热点。