TY - JOUR
T1 - Population structure in admixed populations
T2 - Effect of admixture dynamics on the pattern of linkage disequilibrium
AU - Pfaff, C. L.
AU - Parra, E. J.
AU - Bonilla, C.
AU - Hiester, K.
AU - McKeigue, P. M.
AU - Kamboh, M. I.
AU - Hutchinson, R. G.
AU - Ferrell, R. E.
AU - Boerwinkle, E.
AU - Shriver, M. D.
N1 - Funding Information:
We would like to thank the populations of Jackson, MS, and South Carolina, for their participation in this study. Thanks also go to Ken Weiss and Andy Clark, for comments, suggestions, and critiques of earlier versions of the manuscript, and to Jeff Long, for providing some of the computer programs used in the analysis. This research has been supported in part by grants from the National Institutes of Health: National Human Genome Research Institute grant HG02154 and National Institute of Diabetes & Digestive & Kidney Diseases grant DK53958 (both to M.D.S) and National Heart, Lung, and Blood Institute grant HL44672 (to M.I.K.).
PY - 2001
Y1 - 2001
N2 - Gene flow 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.
AB - Gene flow 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.
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U2 - 10.1086/316935
DO - 10.1086/316935
M3 - Article
C2 - 11112661
AN - SCOPUS:0035163561
SN - 0002-9297
VL - 68
SP - 198
EP - 207
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 1
ER -