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本文引用的文献

1
Genome-wide detection and characterization of positive selection in human populations.人类群体中正选择的全基因组检测与特征分析。
Nature. 2007 Oct 18;449(7164):913-8. doi: 10.1038/nature06250.
2
A second generation human haplotype map of over 3.1 million SNPs.一张包含超过310万个单核苷酸多态性的第二代人类单倍型图谱。
Nature. 2007 Oct 18;449(7164):851-61. doi: 10.1038/nature06258.
3
Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2.色素沉着相关基因SLC24A5和SLC45A2中两个编码单核苷酸多态性的人群差异。
Int J Legal Med. 2007 Jan;121(1):36-9. doi: 10.1007/s00414-006-0112-z. Epub 2006 Jul 18.
4
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans.溶质载体家族24成员5(SLC24A5)是一种假定的阳离子交换剂,它会影响斑马鱼和人类的色素沉着。
Science. 2005 Dec 16;310(5755):1782-6. doi: 10.1126/science.1116238.
5
A haplotype map of the human genome.人类基因组单倍型图谱。
Nature. 2005 Oct 27;437(7063):1299-320. doi: 10.1038/nature04226.
6
Genetics of hair and skin color.头发和肤色的遗传学
Annu Rev Genet. 2003;37:67-90. doi: 10.1146/annurev.genet.37.110801.143233.
7
A classifier for the SNP-based inference of ancestry.一种用于基于单核苷酸多态性(SNP)推断祖先的分类器。
J Forensic Sci. 2003 Jul;48(4):771-82.
8
Apportionment of global human genetic diversity based on craniometrics and skin color.基于颅骨测量学和肤色的全球人类遗传多样性分配
Am J Phys Anthropol. 2002 Aug;118(4):393-8. doi: 10.1002/ajpa.10079.
9
Inferring ethnic origin by means of an STR profile.
Forensic Sci Int. 2001 Jun 1;119(1):17-22. doi: 10.1016/s0379-0738(00)00387-x.
10
A new statistical method for haplotype reconstruction from population data.一种从群体数据中重建单倍型的新统计方法。
Am J Hum Genet. 2001 Apr;68(4):978-89. doi: 10.1086/319501. Epub 2001 Mar 9.

SLC24A5 基因单倍型作为不同人群的祖籍信息标记。

Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations.

机构信息

Centre of Excellence for Genomic Risk Assessment in Multifactorial and Complex Diseases, School of Medicine, Tor Vergata University of Rome, Italy.

出版信息

Curr Genomics. 2008 Apr;9(2):110-4. doi: 10.2174/138920208784139528.

DOI:10.2174/138920208784139528
PMID:19440451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2674805/
Abstract

Ancestry informative markers (AIMs) are human polymorphisms that exhibit substantially allele frequency differences among populations. These markers can be useful to provide information about ancestry of samples which may be useful in predicting a perpetrator's ethnic origin to aid criminal investigations. Variations in human pigmentation are the most obvious phenotypes to distinguish individuals. It has been recently shown that the variation of a G in an A allele of the coding single-nucleotide polymorphism (SNP) rs1426654 within SLC24A5 gene varies in frequency among several population samples according to skin pigmentation. Because of these observations, the SLC24A5 locus has been evaluated as Ancestry Informative Region (AIR) by typing rs1426654 together with two additional intragenic markers (rs2555364 and rs16960620) in 471 unrelated individuals originating from three different continents (Africa, Asia and Europe). This study further supports the role of human SLC24A5 gene in skin pigmentation suggesting that variations in SLC24A5 haplotypes can correlate with human migration and ancestry. Furthermore, our data do reveal the utility of haplotype and combined unphased genotype analysis of SLC24A5 in predicting ancestry and provide a good example of usefulness of genetic characterization of larger regions, in addition to single polymorphisms, as candidates for population-specific sweeps in the ancestral population.

摘要

祖源信息标记 (AIMs) 是人类多态性,在不同人群中表现出显著的等位基因频率差异。这些标记可以提供有关样本祖源的信息,这可能有助于预测犯罪者的种族起源,以协助刑事调查。人类色素沉着的变化是区分个体最明显的表型。最近已经表明,编码单核苷酸多态性 (SNP) rs1426654 中的 A 等位基因中的 G 变异在根据皮肤色素沉着的几个人群样本中的频率不同。由于这些观察结果,SLC24A5 基因座已被评估为祖源信息区 (AIR),通过在来自三个不同大陆(非洲、亚洲和欧洲)的 471 个无关个体中一起对 rs1426654 以及两个额外的内含子标记 (rs2555364 和 rs16960620) 进行分型。这项研究进一步支持了人类 SLC24A5 基因在皮肤色素沉着中的作用,表明 SLC24A5 单倍型的变异可以与人类迁移和祖源相关。此外,我们的数据确实揭示了 SLC24A5 单倍型和组合无相位基因型分析在预测祖源方面的效用,并提供了一个很好的例子,即除了单核苷酸多态性之外,对更大区域的遗传特征作为祖先群体中特定人群的选择候选物的有用性。