Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications

被引:292
作者
Ballantyne, Kaye N. [1 ]
Goedbloed, Miriam [1 ]
Fang, Rixun [2 ]
Schaap, Onno [1 ]
Lao, Oscar [1 ]
Wollstein, Andreas [3 ]
Choi, Ying [1 ]
van Duijn, Kate [1 ]
Vermeulen, Mark [1 ]
Brauer, Silke [1 ,4 ]
Decorte, Ronny [5 ,6 ]
Poetsch, Micaela [7 ]
von Wurmb-Schwark, Nicole [8 ]
de Knijff, Peter [9 ]
Labuda, Damian [10 ]
Vezina, Helene [11 ]
Knoblauch, Hans [12 ]
Lessig, Ruediger [13 ]
Roewer, Lutz [14 ]
Ploski, Rafal [15 ,16 ]
Dobosz, Tadeusz [17 ]
Henke, Lotte [18 ]
Henke, Juegen [18 ]
Furtado, Manohar R. [2 ]
Kayser, Manfred [1 ]
机构
[1] Erasmus MC, Dept Forens Mol Biol, NL-3000 CA Rotterdam, Netherlands
[2] Life Technol, Foster City, CA 94404 USA
[3] Univ Cologne, Cologne Ctr Genom, D-50674 Cologne, Germany
[4] Netherlands Forens Inst, NL-2497 GB The Hague, Netherlands
[5] Univ Hosp KU Leuven, Dept Forens Med, B-3000 Louvain, Belgium
[6] Univ Hosp KU Leuven, Ctr Human Genet, B-3000 Louvain, Belgium
[7] Univ Hosp Essen, Inst Legal Med, D-45122 Essen, Germany
[8] Univ Schleswig Holstein, Inst Legal Med, D-24105 Kiel, Germany
[9] Leiden Univ, Med Ctr, Dept Human & Clin Genet, Forens Lab DNA Res, NL-2300 RC Leiden, Netherlands
[10] Univ Montreal, Dept Pediat, CHU St Justine, Ctr Rech, Montreal, PQ H3T 1C5, Canada
[11] Univ Quebec Chicoutimi, Interdisciplinary Res Grp Demog & Genet Epidemiol, Chicoutimi, PQ G7H 2B1, Canada
[12] Charite, Abt Myol, Expt & Clin Res Ctr, D-10117 Berlin, Germany
[13] Univ Leipzig, Inst Legal Med, D-04103 Leipzig, Germany
[14] Charite, Abt Forens Genet, Inst Rechtsmed & Forens Wissensch, D-10115 Berlin, Germany
[15] Med Univ Warsaw, Dept Med Genet, PL-02007 Warsaw, Poland
[16] Med Univ Warsaw, Dept Forens Med, PL-02007 Warsaw, Poland
[17] Wroclaw Med Univ, Dept Forens Med, PL-50368 Wroclaw, Poland
[18] Inst Blutgruppenforsch LGC GmbH, D-50933 Cologne, Germany
关键词
SHORT TANDEM REPEATS; MUTATION-RATES; HAPLOGROUP TREE; DNA-SEQUENCES; HUMAN GENOME; EVOLUTION; LENGTH; HUMANS; LOCI; SLIPPAGE;
D O I
10.1016/j.ajhg.2010.08.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nonrecombining Y-chromosomal microsatellites (Y-STRs) are widely used to infer population histories, discover genealogical relationships, and identify males for criminal justice purposes. Although a key requirement for their application is reliable mutability knowledge, empirical data are only available for a small number of Y-STRs thus far. To rectify this, we analyzed a large number of 186 Y-STR markers in nearly 2000 DNA-confirmed father-son pairs, covering an overall number of 352,999 meiotic transfers. Following confirmation by DNA sequence analysis, the retrieved mutation data were modeled via a Bayesian approach, resulting in mutation rates from 3.78 x 10(-4) (95% credible interval [CI], 1.38 x 10(-5) - 2.02 x 10(-3)) to 7.44 x 10(-2) (95% Cl, 6.51 x 10(-2) - 9.09 x 10(-2)) per marker per generation. With the 924 mutations at 120 Y-STR markers, a nonsignificant excess of repeat losses versus gains (1.16:1), as well as a strong and significant excess of single-repeat versus multirepeat changes (25.23:1), was observed. Although the total repeat number influenced Y-STR locus mutability most strongly, repeat complexity, the length in base pairs of the repeated motif, and the father's age also contributed to Y-STR mutability. To exemplify how to practically utilize this knowledge, we analyzed the 13 most mutable Y-STRs in an independent sample set and empirically proved their suitability for distinguishing close and distantly related males. This finding is expected to revolutionize Y-chromosomal applications in forensic biology, from previous male lineage differentiation toward future male individual identification.
引用
收藏
页码:341 / 353
页数:13
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