Literature DB >> 29573605

Expanded Croatian 12 X-STR loci database with an overview of anomalous profiles.

Gordan Mršić1, Petar Ozretić2, Josip Crnjac3, Siniša Merkaš1, Viktorija Sukser1, Ivana Račić1, Sara Rožić1, Lucija Barbarić1, Maja Popović4, Marina Korolija5.   

Abstract

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.
Copyright © 2018 Elsevier B.V. All rights reserved.

Keywords:  Anomalous X-STR profiles; Croatian X-STR database; Forensic X-STR markers; Investigator(®) Argus X-12; Locus DXS10079; X chromosome duplication

Mesh:

Year:  2018        PMID: 29573605     DOI: 10.1016/j.fsigen.2018.03.004

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  2 in total

1.  Polymorphism and haplotype analysis of three novel short tandem repeat loci in the p11.4 region of human X chromosome.

Authors:  Takeki Nishi; Kenji Fukui; Sari Matumoto; Shojiro Takasu; Kimiharu Iwadate
Journal:  Int J Legal Med       Date:  2021-11-06       Impact factor: 2.791

Review 2.  Forensic Applications of Markers Present on the X Chromosome.

Authors:  Fernanda M Garcia; Bárbara G O Bessa; Eldamária V W Dos Santos; Julia D P Pereira; Lyvia N R Alves; Lucas A Vianna; Matheus C Casotti; Raquel S R Trabach; Victor S Stange; Débora D Meira; Iuri D Louro
Journal:  Genes (Basel)       Date:  2022-09-07       Impact factor: 4.141

  2 in total

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