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Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit

The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpFlSTR® Yfiler® polymerase chain reaction amplification kit have become widely used for forensic and evolutionary applications where a reliable knowledge on mutation properties is necessary for correct data interpretation....

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Autores principales: Goedbloed, Miriam, Vermeulen, Mark, Fang, Rixun N., Lembring, Maria, Wollstein, Andreas, Ballantyne, Kaye, Lao, Oscar, Brauer, Silke, Krüger, Carmen, Roewer, Lutz, Lessig, Rüdiger, Ploski, Rafal, Dobosz, Tadeusz, Henke, Lotte, Henke, Jürgen, Furtado, Manohar R., Kayser, Manfred
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766043/
https://www.ncbi.nlm.nih.gov/pubmed/19322579
http://dx.doi.org/10.1007/s00414-009-0342-y
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author Goedbloed, Miriam
Vermeulen, Mark
Fang, Rixun N.
Lembring, Maria
Wollstein, Andreas
Ballantyne, Kaye
Lao, Oscar
Brauer, Silke
Krüger, Carmen
Roewer, Lutz
Lessig, Rüdiger
Ploski, Rafal
Dobosz, Tadeusz
Henke, Lotte
Henke, Jürgen
Furtado, Manohar R.
Kayser, Manfred
author_facet Goedbloed, Miriam
Vermeulen, Mark
Fang, Rixun N.
Lembring, Maria
Wollstein, Andreas
Ballantyne, Kaye
Lao, Oscar
Brauer, Silke
Krüger, Carmen
Roewer, Lutz
Lessig, Rüdiger
Ploski, Rafal
Dobosz, Tadeusz
Henke, Lotte
Henke, Jürgen
Furtado, Manohar R.
Kayser, Manfred
author_sort Goedbloed, Miriam
collection PubMed
description The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpFlSTR® Yfiler® polymerase chain reaction amplification kit have become widely used for forensic and evolutionary applications where a reliable knowledge on mutation properties is necessary for correct data interpretation. Therefore, we investigated the 17 Yfiler Y-STRs in 1,730–1,764 DNA-confirmed father–son pairs per locus and found 84 sequence-confirmed mutations among the 29,792 meiotic transfers covered. Of the 84 mutations, 83 (98.8%) were single-repeat changes and one (1.2%) was a double-repeat change (ratio, 1:0.01), as well as 43 (51.2%) were repeat gains and 41 (48.8%) repeat losses (ratio, 1:0.95). Medians from Bayesian estimation of locus-specific mutation rates ranged from 0.0003 for DYS448 to 0.0074 for DYS458, with a median rate across all 17 Y-STRs of 0.0025. The mean age (at the time of son’s birth) of fathers with mutations was with 34.40 (±11.63) years higher than that of fathers without ones at 30.32 (±10.22) years, a difference that is highly statistically significant (p < 0.001). A Poisson-based modeling revealed that the Y-STR mutation rate increased with increasing father’s age on a statistically significant level (α = 0.0294, 2.5% quantile = 0.0001). From combining our data with those previously published, considering all together 135,212 meiotic events and 331 mutations, we conclude for the Yfiler Y-STRs that (1) none had a mutation rate of >1%, 12 had mutation rates of >0.1% and four of <0.1%, (2) single-repeat changes were strongly favored over multiple-repeat ones for all loci but 1 and (3) considerable variation existed among loci in the ratio of repeat gains versus losses. Our finding of three Y-STR mutations in one father–son pair (and two pairs with two mutations each) has consequences for determining the threshold of allelic differences to conclude exclusion constellations in future applications of Y-STRs in paternity testing and pedigree analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00414-009-0342-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-27660432009-10-26 Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit Goedbloed, Miriam Vermeulen, Mark Fang, Rixun N. Lembring, Maria Wollstein, Andreas Ballantyne, Kaye Lao, Oscar Brauer, Silke Krüger, Carmen Roewer, Lutz Lessig, Rüdiger Ploski, Rafal Dobosz, Tadeusz Henke, Lotte Henke, Jürgen Furtado, Manohar R. Kayser, Manfred Int J Legal Med Original Article The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpFlSTR® Yfiler® polymerase chain reaction amplification kit have become widely used for forensic and evolutionary applications where a reliable knowledge on mutation properties is necessary for correct data interpretation. Therefore, we investigated the 17 Yfiler Y-STRs in 1,730–1,764 DNA-confirmed father–son pairs per locus and found 84 sequence-confirmed mutations among the 29,792 meiotic transfers covered. Of the 84 mutations, 83 (98.8%) were single-repeat changes and one (1.2%) was a double-repeat change (ratio, 1:0.01), as well as 43 (51.2%) were repeat gains and 41 (48.8%) repeat losses (ratio, 1:0.95). Medians from Bayesian estimation of locus-specific mutation rates ranged from 0.0003 for DYS448 to 0.0074 for DYS458, with a median rate across all 17 Y-STRs of 0.0025. The mean age (at the time of son’s birth) of fathers with mutations was with 34.40 (±11.63) years higher than that of fathers without ones at 30.32 (±10.22) years, a difference that is highly statistically significant (p < 0.001). A Poisson-based modeling revealed that the Y-STR mutation rate increased with increasing father’s age on a statistically significant level (α = 0.0294, 2.5% quantile = 0.0001). From combining our data with those previously published, considering all together 135,212 meiotic events and 331 mutations, we conclude for the Yfiler Y-STRs that (1) none had a mutation rate of >1%, 12 had mutation rates of >0.1% and four of <0.1%, (2) single-repeat changes were strongly favored over multiple-repeat ones for all loci but 1 and (3) considerable variation existed among loci in the ratio of repeat gains versus losses. Our finding of three Y-STR mutations in one father–son pair (and two pairs with two mutations each) has consequences for determining the threshold of allelic differences to conclude exclusion constellations in future applications of Y-STRs in paternity testing and pedigree analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00414-009-0342-y) contains supplementary material, which is available to authorized users. Springer-Verlag 2009-03-26 2009 /pmc/articles/PMC2766043/ /pubmed/19322579 http://dx.doi.org/10.1007/s00414-009-0342-y Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Goedbloed, Miriam
Vermeulen, Mark
Fang, Rixun N.
Lembring, Maria
Wollstein, Andreas
Ballantyne, Kaye
Lao, Oscar
Brauer, Silke
Krüger, Carmen
Roewer, Lutz
Lessig, Rüdiger
Ploski, Rafal
Dobosz, Tadeusz
Henke, Lotte
Henke, Jürgen
Furtado, Manohar R.
Kayser, Manfred
Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title_full Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title_fullStr Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title_full_unstemmed Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title_short Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
title_sort comprehensive mutation analysis of 17 y-chromosomal short tandem repeat polymorphisms included in the ampflstr® yfiler® pcr amplification kit
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2766043/
https://www.ncbi.nlm.nih.gov/pubmed/19322579
http://dx.doi.org/10.1007/s00414-009-0342-y
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