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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/4247

Title: Genomic complexity of the Y-STR DYS19: inversions, deletions and founder lineages carrying duplications.
Authors: Balaresque, Patricia L.
Parkin, Emma J.
Roewer, Lutz
Carvalho-Silva, Denise R.
Mitchell, R. John
van Oorschot, Roland A.H.
Henke, Jürgen
Stoneking, Mark
Nasidze, Ivan
Wetton, Jon
de Knijff, Peter
Tyler-Smith, Chris
Jobling, Mark A.
Issue Date: Jan-2009
Publisher: Springer Verlag
Citation: International Journal of Legal Medicine, 2009, 123 (1), pp. 15-23.
Abstract: The Y-STR DYS19 is firmly established in the repertoire of Y-chromosomal markers used in forensic analysis yet is poorly understood at the molecular level, lying in a complex genomic environment and exhibiting null alleles, as well as duplications and occasional triplications in population samples. Here, we analyse three null alleles and 51 duplications and show that DYS19 can also be involved in inversion events, so that even its location within the short arm of the Y chromosome is uncertain. Deletion mapping in the three chromosomes carrying null alleles shows that their deletions are less than ∼300 kb in size. Haplotypic analysis with binary markers shows that they belong to three different haplogroups and so represent independent events. In contrast, a collection of 51 DYS19 duplication chromosomes belong to only four haplogroups: two are singletons and may represent somatic mutation in lymphoblastoid cell lines, but two, in haplogroups G and C3c, represent founder lineages that have spread widely in Central Europe/West Asia and East Asia, respectively. Consideration of candidate mechanisms underlying both deletions and duplications provides no evidence for the involvement of non-allelic homologous recombination, and they are likely to represent sporadic events with low mutation rates. Understanding the basis and population distribution of these DYS19 alleles will aid in the utilisation and interpretation of profiles that contain them.
ISSN: 0937-9827
Links: http://dx.doi.org/10.1007/s00414-008-0253-3
http://hdl.handle.net/2381/4247
Type: Article
Description: This is the author's final draft of the paper published as International Journal of Legal Medicine, 2009, 123 (1), pp. 15-23. The original publication is available at www.springerlink.com. Doi: 10.1007/s00414-008-0253-3
Appears in Collections:Published Articles, Dept. of Genetics

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