Skin pigmentation, biogeographical ancestry and admixture mapping

被引:379
作者
Shriver, MD
Parra, EJ
Dios, S
Bonilla, C
Norton, H
Jovel, C
Pfaff, C
Jones, C
Massac, A
Cameron, N
Baron, A
Jackson, T
Argyropoulos, G
Jin, L
Hoggart, CJ
McKeigue, PM
Kittles, RA
机构
[1] Penn State Univ, Dept Anthropol, University Pk, PA 16802 USA
[2] Howard Univ, Natl Human Genome Ctr, Washington, DC 20060 USA
[3] Takeway Media, London EC1R 0BD, England
[4] Pennington Biomed Res Ctr, Baton Rouge, LA USA
[5] Univ Cincinnati, Dept Environm Hlth, Cincinnati, OH USA
[6] Univ London London Sch Hyg & Trop Med, Dept Epidemiol & Populat Hlth, London WC1E 7HT, England
关键词
D O I
10.1007/s00439-002-0896-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ancestry informative markers (AIMs) are genetic loci showing alleles with large frequency differences between populations. AIMs can be used to estimate biogeographical ancestry at the level of the population, subgroup (e.g. cases and controls) and individual. Ancestry estimates at both the subgroup and individual level can be directly instructive regarding the genetics of the phenotypes that differ qualitatively or in frequency between populations. These estimates can provide a compelling foundation for the use of admixture mapping (AM) methods to identify the genes underlying these traits. We present details of a panel of 34 AIMs and demonstrate how such studies can proceed, by using skin pigmentation as a model phenotype. We have genotyped these markers in two population samples with primarily African ancestry, viz. African Americans from Washington D.C. and an African Caribbean sample from Britain, and in a sample of European Americans from Pennsylvania. In the two African population samples, we observed significant correlations between estimates of individual ancestry and skin pigmentation as measured by reflectometry (R-2 = 0.21, P < 0.0001 for the African-American sample and R-2 = 0.16, P < 0.0001 for the British African-Caribbean sample). These correlations confirm the validity of the ancestry estimates and also indicate the high level of population structure related to admixture, a level that characterizes these populations and that is detectable by using other tests to identify genetic structure. We have also applied two methods of admixture mapping to test for the effects of three candidate genes (TYR, OCA2, MC1R) on pigmentation. We show that TYR and OCA2 have measurable effects on skin pigmentation differences between the west African and west European parental populations. This work indicates that it is possible to estimate the individual ancestry of a person based on DNA analysis with a reasonable number of well-defined genetic markers. The implications and applications of ancestry estimates in biomedical research are discussed.
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收藏
页码:387 / 399
页数:13
相关论文
共 53 条
[1]   Melting curve analysis of SNPs (McSNP®):: A gel-free and inexpensive approach for SNP genotyping [J].
Akey, JM ;
Sosnoski, D ;
Parra, E ;
Dios, S ;
Hiester, K ;
Su, B ;
Bonilla, C ;
Jin, L ;
Shriver, MD .
BIOTECHNIQUES, 2001, 30 (02) :358-+
[2]   Interaction between the melanocortin-1 receptor and P genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population [J].
Akey, JM ;
Wang, H ;
Xiong, M ;
Wu, H ;
Liu, W ;
Shriver, MD ;
Jin, L .
HUMAN GENETICS, 2001, 108 (06) :516-520
[3]  
[Anonymous], 1991, Biological perspectives on human pigmentation
[4]   The genetics of pigmentation: From fancy genes to complex traits [J].
Barsh, GS .
TRENDS IN GENETICS, 1996, 12 (08) :299-305
[5]   The melanocortin-1-receptor gene is the major freckle gene [J].
Bastiaens, M ;
ter Huurne, J ;
Gruis, N ;
Bergman, W ;
Westendorp, R ;
Vermeer, BJ ;
Bavinck, JNB .
HUMAN MOLECULAR GENETICS, 2001, 10 (16) :1701-1708
[6]   Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair [J].
Bastiaens, MT ;
ter Huurne, JAC ;
Kielich, C ;
Gruis, NA ;
Westendorp, RGJ ;
Vermeer, BJ ;
Bavinck, NJB .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (04) :884-894
[7]  
Brilliant MH, 2001, PIGM CELL RES, V14, P86, DOI 10.1034/j.1600-0749.2001.140203.x
[8]  
BRISCOE D, 1994, J HERED, V85, P59
[9]  
BYARD PJ, 1981, YEARB PHYS ANTHROPOL, V24, P123
[10]   ADMIXTURE AS A TOOL FOR FINDING LINKED GENES AND DETECTING THAT DIFFERENCE FROM ALLELIC ASSOCIATION BETWEEN LOCI [J].
CHAKRABORTY, R ;
WEISS, KM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9119-9123