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Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications.

Authors :
Ballantyne KN
Goedbloed M
Fang R
Schaap O
Lao O
Wollstein A
Choi Y
van Duijn K
Vermeulen M
Brauer S
Decorte R
Poetsch M
von Wurmb-Schwark N
de Knijff P
Labuda D
Vézina H
Knoblauch H
Lessig R
Roewer L
Ploski R
Dobosz T
Henke L
Henke J
Furtado MR
Kayser M
Source :
American journal of human genetics [Am J Hum Genet] 2010 Sep 10; Vol. 87 (3), pp. 341-53.
Publication Year :
2010

Abstract

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 × 10(-4) (95% credible interval [CI], 1.38 × 10(-5) - 2.02 × 10(-3)) to 7.44 × 10(-2) (95% CI, 6.51 × 10(-2) - 9.09 × 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.<br /> (2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
87
Issue :
3
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
20817138
Full Text :
https://doi.org/10.1016/j.ajhg.2010.08.006