Population structure in admired populations: Effect of admixture dynamics on the pattern of linkage disequilibrium

被引:195
作者
Pfaff, CL
Parra, EJ
Bonilla, C
Hiester, K
McKeigue, PM
Kamboh, MI
Hutchinson, RG
Ferrell, RE
Boerwinkle, E
Shriver, MD
机构
[1] Penn State Univ, Dept Anthropol, University Pk, PA 16802 USA
[2] London Sch Hyg & Trop Med, Dept Epidemiol & Populat Hlth, London, England
[3] Univ Pittsburgh, Dept Human Genet, Pittsburgh, PA USA
[4] Univ Mississippi, Med Ctr, Dept Med, Jackson, MS 39216 USA
[5] Univ Texas, Ctr Human Genet, Houston, TX USA
[6] Univ Texas, Inst Mol Med, Houston, TX USA
基金
美国国家卫生研究院;
关键词
D O I
10.1086/316935
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene now between genetically distinct populations creates linkage disequilibrium (admixture linkage disequilibrium [ALD]) among all loci (linked and unlinked) that have different allele frequencies in the founding populations, We have explored the distribution of ALD by using computer simulation of two extreme models of admixture: the hybrid-isolation (HI) model, in which admixture occurs in a single generation, and the continuous-gene-flow (CGF) model, in which admixture occurs at a steady rate in every generation. Linkage disequilibrium patterns in African American population samples from Jackson, MS, and from coastal South Carolina resemble patterns observed in the simulated CGF populations, in two respects. First, significant association between two loci (FY and AT3) separated by 22 cM was detected in both samples. The retention of ALD over relatively large (>10 cM) chromosomal segments is characteristic of a CGF pattern of admixture but not of an HI pattern. Second, significant associations were also detected between many pairs of unlinked loci, as observed in the CGF simulation results but not in the simulated HI populations. Such a high rate of association between unlinked markers in these populations could result in false-positive linkage signals in an admixture-mapping study. However, we demonstrate that by conditioning on parental admixture, we can distinguish between true linkage and association resulting from shared ancestry. Therefore, populations with a CGF history of admixture not only are appropriate for admixture mapping but also have greater power for detection of linkage disequilibrium over large chromosomal regions than do populations that have experienced a pattern of admixture more similar to the HI model, if methods are employed that detect and adjust for disequilibrium caused by continuous admixture.
引用
收藏
页码:198 / 207
页数:10
相关论文
共 24 条
[11]  
LONG JC, 1995, AM J HUM GENET, V56, P799
[12]   Mapping genes that underlie ethnic differences in disease risk: Methods for detecting linkage in admixed populations, by conditioning on parental admixture [J].
McKeigue, PM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :241-251
[13]  
McKeigue PM, 2000, ANN HUM GENET, V64, P171, DOI 10.1017/S0003480000008022
[14]  
McKeigue PM, 1997, AM J HUM GENET, V60, P188
[15]   Estimating African American admixture proportions by use of population-specific alleles [J].
Parra, EJ ;
Marcini, A ;
Akey, L ;
Martinson, J ;
Batzer, MA ;
Cooper, R ;
Forrester, T ;
Allison, DB ;
Deka, R ;
Ferrell, RE ;
Shriver, MD .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (06) :1839-1851
[16]  
PARRA EJ, IN PRESS AM J PHYS A
[17]   Use of unlinked genetic markers to detect population stratification in association studies [J].
Pritchard, JK ;
Rosenberg, NA .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (01) :220-228
[18]   The future of genetic studies of complex human diseases [J].
Risch, N ;
Merikangas, K .
SCIENCE, 1996, 273 (5281) :1516-1517
[19]  
Shriver MD, 1997, AM J HUM GENET, V60, P957
[20]  
Sokal R. R., 1995, BIOMETRY PRINCIPLES