Validation of the X-chromosomal STR DXS6809

被引:24
|
作者
Edelmann, J
Deichsel, D
Plate, I
Käser, M
Szibor, R
机构
[1] Univ Leipzig, Inst Rechtsmed, D-04103 Leipzig, Germany
[2] Lab Hamogenet, Baden Baden, Germany
[3] Univ Magdeburg, Inst Rechtsmed, D-39106 Magdeburg, Germany
关键词
short tandem repeats; X-chromosome; population genetics; repeat sequence; mutation rate;
D O I
10.1007/s00414-003-0369-4
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
This paper presents sequence and population genetic data of the microsatellite marker DXS6809 (GDB 365492) obtained from a German population sample (n=725 chromosomes). DXS6809 is a highly polymorphic X-linked tetranucleotide polymorphism presenting 12 alleles in our population. Sequencing of 77 PCR products covering 12 alleles (by length), characterised DXS6809 as a marker with a complex repeat sequence structure. A polymorphism information content (PIC) of 0.825 and a mean exclusion chance (MEC) of 0.815 were obtained. A deviation from the Hardy-Weinberg equilibrium (HWE) could not be detected and male and female samples exhibited a similar allele distribution. Kinship testing revealed a typical X-linked inheritance and 2 mutations were found in 394 meioses. DXS6809 is located 90.18 Mb, i.e. 102.3 cM, from the Xp-telomere (Xp-tel), corresponding to Xq21.33. The presented data qualify DXS6809 as a useful supplement to the known forensic ChrX marker panel.
引用
收藏
页码:241 / 244
页数:4
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