Literature DB >> 19693525

SNPSTR rs59186128_D7S820 polymorphism distribution in European Caucasoid, Hispanic, and Afro-American populations.

A Odriozola1, J M Aznar, L Valverde, S Cardoso, M L Bravo, J J Builes, B Martínez, D Sanchez, F González-Andrade, E Sarasola, M C González-Fernández, B Martínez Jarreta, Marian M De Pancorbo.   

Abstract

Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help distinguish between STR alleles in which the number of repetitions matches due to descent from those which match by chance. This provides support for the determination of biological paternity and other kinship analyses in which mutation needs to be ruled out as grounds for exclusion. Locus D7S820 shows a variable position, SNP rs59186128, in the 5' flanking region. This study is set out (1) to determine the frequencies of SNP rs59186128 in populations with various geographical origins and (2) to estimate the possible contribution of rs59186128 to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus rs59186128 to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR rs59186128_D7820. The results show that SNP rs59186128 has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR rs59186128_D7S820, which supports the idea that they could be useful in forensic applications.

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Year:  2009        PMID: 19693525     DOI: 10.1007/s00414-009-0370-7

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  26 in total

1.  Heterogeneous mutation processes in human microsatellite DNA sequences.

Authors:  H Ellegren
Journal:  Nat Genet       Date:  2000-04       Impact factor: 38.330

2.  Mutations at Y-STR loci: implications for paternity testing and forensic analysis.

Authors:  M Kayser; A Sajantila
Journal:  Forensic Sci Int       Date:  2001-05-15       Impact factor: 2.395

Review 3.  Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review.

Authors:  You-Chun Li; Abraham B Korol; Tzion Fahima; Avigdor Beiles; Eviatar Nevo
Journal:  Mol Ecol       Date:  2002-12       Impact factor: 6.185

4.  Validation of a 16-locus fluorescent multiplex system.

Authors:  Benjamin E Krenke; Allan Tereba; Stacey J Anderson; Eric Buel; Sherry Culhane; Carla J Finis; Christine S Tomsey; Jeffrey M Zachetti; Arni Masibay; Dawn R Rabbach; Elizabeth A Amiott; Cynthia J Sprecher
Journal:  J Forensic Sci       Date:  2002-07       Impact factor: 1.832

5.  Microsatellite instability.

Authors:  Albert de la Chapelle
Journal:  N Engl J Med       Date:  2003-07-17       Impact factor: 91.245

6.  Candidate SNPs for a universal individual identification panel.

Authors:  Andrew J Pakstis; William C Speed; Judith R Kidd; Kenneth K Kidd
Journal:  Hum Genet       Date:  2007-02-27       Impact factor: 4.132

7.  The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project.

Authors:  Jorge Amigo; Christopher Phillips; Maviky Lareu; Angel Carracedo
Journal:  Int J Legal Med       Date:  2008-05-20       Impact factor: 2.686

8.  Possible pitfalls in motherless paternity analysis with related putative fathers.

Authors:  Nicole von Wurmb-Schwark; Victoria Mályusz; Eva Simeoni; Eberhard Lignitz; Micaela Poetsch
Journal:  Forensic Sci Int       Date:  2005-09-06       Impact factor: 2.395

Review 9.  Human DNA repair genes, 2005.

Authors:  Richard D Wood; Michael Mitchell; Tomas Lindahl
Journal:  Mutat Res       Date:  2005-09-04       Impact factor: 2.433

10.  SNPSTR: a database of compound microsatellite-SNP markers.

Authors:  I Agrafioti; M P H Stumpf
Journal:  Nucleic Acids Res       Date:  2007-01       Impact factor: 16.971

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  1 in total

1.  Utility of ForenSeq™ DNA Signature Prep Kit in the research of pairwise 2nd-degree kinship identification.

Authors:  Miao Xu; Qingqing Du; Guanju Ma; Zifan Chen; Qingxia Liu; Lihong Fu; Bin Cong; Shujin Li
Journal:  Int J Legal Med       Date:  2019-01-28       Impact factor: 2.686

  1 in total

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