Evaluation of Y-chromosomal STRs: A multicenter study

被引:597
作者
Kayser, M
Caglia, A
Corach, D
Fretwell, N
Gehrig, C
Graziosi, G
Heidorn, F
Herrmann, S
Herzog, B
Hidding, M
Honda, K
Jobling, M
Krawczak, M
Leim, K
Meuser, S
Meyer, E
Oesterreich, W
Pandya, A
Parson, W
Penacino, G
PerezLezaun, A
Piccinini, A
Prinz, M
Schmitt, C
Schneider, PM
Szibor, R
TeifelGreding, J
Weichold, G
deKnijff, P
Roewer, L
机构
[1] INST GERICHTLICHE MED, D-10115 BERLIN, GERMANY
[2] UNIV CATTOLICA SACRO CUORE, INST MED LEGALE, I-00168 ROME, ITALY
[3] UNIV BUENOS AIRES, FAC FARM & BIOQUIM, SERV HUELLAS DIGITALES GENET, RA-1113 BUENOS AIRES, DF, ARGENTINA
[4] UNIV LEICESTER, DEPT GENET, LEICESTER LE1 7RH, LEICS, ENGLAND
[5] INST RECHTSMED, CH-3012 BERN, SWITZERLAND
[6] UNIV TRIESTE, DEPT BIOL, I-34127 TRIESTE, ITALY
[7] INST RECHTSMED, D-14195 BERLIN, GERMANY
[8] LANDESKRIMINALAMT BERLIN, D-10823 BERLIN, GERMANY
[9] INST RECHTSMED, D-07743 JENA, GERMANY
[10] INST RECHTSMED, D-50823 COLOGNE, GERMANY
[11] OSAKA UNIV, SCH MED, DEPT LEGAL MED, SUITA, OSAKA 565, JAPAN
[12] UNIV WALES COLL CARDIFF, INST MED GENET, CARDIFF CF4 4XN, S GLAM, WALES
[13] INST RECHTSMED, D-69115 HEIDELBERG, GERMANY
[14] INST RECHTSMED, D-55131 MAINZ, GERMANY
[15] INST RECHTSMED, D-48149 MUNSTER, GERMANY
[16] LANDESKRIMINALAMT BRANDENBURG, D-163529 BASDORF, GERMANY
[17] UNIV OXFORD, DEPT BIOCHEM, CRC, CHROMOSOME MOL BIOL GRP, OXFORD OX1 3QU, ENGLAND
[18] INST GERICHTLICHE MED, A-6020 INNSBRUCK, AUSTRIA
[19] UNIV BARCELONA, FAC BIOL, DEPT ANTHROPOL, E-08028 BARCELONA, SPAIN
[20] UNIV MILAN, INST MED LEGALE, I-20133 MILAN, ITALY
[21] OCME, DEPT FORENS BIOL, NEW YORK, NY 10016 USA
[22] BAYER LANDESKRIMINALAMT, D-80636 MAGDEBURG, GERMANY
[23] INST RECHTS MED, D-80337 MUNICH, GERMANY
[24] LEIDEN UNIV, MGC, DEPT HUMAN GENET, NL-2300 RA LEIDEN, NETHERLANDS
关键词
short tandem repeats; Y chromosome; population analysis; mutation rate; Y haplotype analysis;
D O I
10.1007/s004140050051
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
A multicenter study has been carried out to characterize 13 polymorphic short tandem repeat (STR) systems located on the male specific part of the human Y chromosome (DYS19, DYS288, DYS385, DYS388, DYS389I/II, DYS390, DYS391, DYS392, DYS393, YCAI, YCAII, YCAIII, DXYS156Y). Amplification parameters and electrophoresis protocols including multiplex approaches were compiled. The typing of non-recombining Y loci with uniparental inheritance requires special attention to population substructuring due to prevalent male lineages. To assess the extent of these sub-heterogeneities up to 3825 unrelated males were typed in up to 48 population samples for the respective loci. A consistent repeat based nomenclature for most of the loci has been introduced. Moreover we have estimated the average mutation rate for DYS19 in 626 confirmed father son pairs as 3.2 x 10(-3) (95% confidence interval limits of 0.00041-0.00677), a value which can also be expected for other Y-STR loci with similar repeat structure. Recommendations are given for the forensic application of a basic set of 7 STRs (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393) for standard Y-haplotyping in forensic and paternity casework. We recommend further the inclusion of the highly polymorphic bilocal Y-STRs DYS385, YCAII, YCAIII for a nearly complete individualisation of almost any given unrelated male individual. Together, these results suggest that Y-STR loci are useful markers to identify males and male lineages in forensic practice.
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页码:125 / +
页数:1
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