Bini Carla, Riccardi Laura Natalia, Ceccardi Stefania, Carano Francesco, Sarno Stefania, Luiselli Donata, Pelotti Susi
Department of Medical and Surgical Sciences, DIMEC, Institute of Legal Medicine, University of Bologna, Italy.
Department of Medical and Surgical Sciences, DIMEC, Institute of Legal Medicine, University of Bologna, Italy.
Forensic Sci Int Genet. 2015 Mar;15:127-30. doi: 10.1016/j.fsigen.2014.11.008. Epub 2014 Nov 15.
Requests for solving complex kinship casework involving at least one female are increasing and in these circumstances the analysis of X-chromosomal STR markers plays a relevant role. Actually, it is well known the superior statistical power of X-STRs compared to autosomal markers in solving relationship when two sisters or half-sisters are involved and none of parents is available, in maternity testing or in cases involving close relatives as alternative putative fathers. In addition, the possibility to amplify more loci simultaneously and the strategy based on the analysis of four linkage groups to obtain the X-haplotype provide a powerful and validated tool. Nevertheless, haplotypes frequency distribution in different populations is still needed for calculation of probabilities in relationship testing. Published haplotype frequencies from German population data are available, but in different caseworks we found unreported X-haplotypes. To enlarge the forensic X-chromosome database, we present haplotype frequencies and other parameter of forensic interest obtained from 200 anonymous DNA samples of unrelated Italian males for the four linkage groups included in the Investigator Argus X-12 kit. From the comparison of the Italian sample haplotype frequencies with other populations, significant genetic distances were found with Asian and African populations, but not with Europeans. Finally, casework examples of complex kinship analysis are presented.
涉及至少一名女性的复杂亲缘关系鉴定案件的需求正在增加,在这种情况下,X染色体短串联重复序列(STR)标记的分析发挥着重要作用。实际上,众所周知,在涉及两名姐妹或半姐妹且父母均无法提供的情况下,进行亲子鉴定、产妇检测或涉及近亲作为替代推定父亲的案件中,与常染色体标记相比,X-STR在解决亲属关系方面具有更高的统计效力。此外,同时扩增更多基因座的可能性以及基于四个连锁群分析以获得X单倍型的策略提供了一个强大且经过验证的工具。然而,在亲缘关系检测中计算概率仍需要不同人群中的单倍型频率分布。德国人群数据中已公布了单倍型频率,但在不同的鉴定案件中,我们发现了未报告的X单倍型。为了扩大法医X染色体数据库,我们展示了从200名无关意大利男性的匿名DNA样本中获得的四个连锁群的单倍型频率以及其他法医相关参数,这些样本包含在Investigator Argus X-12试剂盒中。通过将意大利样本的单倍型频率与其他人群进行比较,发现与亚洲和非洲人群存在显著的遗传距离,但与欧洲人群没有。最后,给出了复杂亲缘关系分析的鉴定案件实例。