Evidence map›Paper›PMID 22569803›Full record

ArticleInternational journal of legal medicine2012

Understanding the Y chromosome variation in Korea--relevance of combined haplogroup and haplotype analyses.

Myung Jin Park, Hwan Young Lee, Woo Ick Yang, Kyoung-Jin Shin

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Article in International journal of legal medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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9citing papers in PubMed
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9 citing papers in PubMed.

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5 · Who and what money

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4 authors.

Myung Jin ParkDepartment of Forensic Medicine and Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, South Korea.
Hwan Young Lee
Woo Ick Yang
Kyoung-Jin Shin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We performed a molecular characterization of Korean Y-chromosomal haplogroups using a combination of Y-chromosomal single nucleotide polymorphisms (Y-SNPs) and Y-chromosomal short tandem repeats (Y-STRs). In a test using DNA samples from 706 Korean males, a total of 19 different haplogroups were identified by 26 Y-SNPs including the newly redefined markers (PK4, KL2, and P164) in haplogroup O. When genotyping the SNPs, phylogenetic nonequivalence was found between SNPs M117 and M133, which define haplogroup O3a3c1 (O3a2c1a according to the updated tree of haplogroup O by Yan et al. (European Journal of Human Genetics 19:1013-1015, 2011)), suggesting that the position of the M133 marker should be corrected. We have shown that the haplotypes consisted of DYS392, DYS393, DYS437, DYS438, DYS448, and DYS388 loci, which exhibit a relatively lower mutation rate, can preserve phylogenetic information and hence can be used to roughly distinguish Y-chromosome haplogroups, whereas more rapidly mutating Y-STRs such as DYS449 and DYS458 are useful for differentiating male lineages. However, at the relatively rapidly mutating DYS447, DYS449, DYS458, and DYS464 loci, unusually short alleles and intermediate alleles with common sequence structures are informative for elucidating the substructure within the context of a particular haplogroup. In addition, some deletion mutations in the DYS385 flanking region and the null allele at DYS448 were associated with a single haplogroup background. These high-resolution haplogroup and haplotype data will improve our understanding of regional Y-chromosome variation or recent migration routes and will also help to infer haplogroup background or common ancestry.

Indexed as

Chromosomes, Human, YHaplotypesMicrosatellite RepeatsPolymorphism, Single NucleotideAsian PeopleGenetic MarkersHumansMalePhylogenyPolymerase Chain ReactionRepublic of KoreaGenetic Markers

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