Abstract
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.
MeSH Terms
Africa
African Americans
Alleles
Blacks/genetics
Computer Simulation
Europe
False Positive Reactions
Gene Frequency/genetics
Genetics, Population
Humans
Linkage Disequilibrium/genetics
Mississippi
Models, Genetic
South Carolina
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Pfaff C L
Department of Anthropology, Pennsylvania State University, University Park, PA, 16802, USA.
Parra E J
Bonilla C
Hiester K
McKeigue P M
Kamboh M I
Hutchinson R G
Ferrell R E
Boerwinkle E
Shriver M D
References (23)
23 references, click to expand
-
Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans.
Am J Hum Genet. 2000 Mar;66(3):969-78
PMID: 10712211
-
Mapping genes underlying ethnic differences in disease risk by linkage disequilibrium in recently admixed populations.
Am J Hum Genet. 1997 Jan;60(1):188-96
PMID: 8981962
-
A look at linkage disequilibrium.
Nat Genet. 2000 Jul;25(3):246-7
PMID: 10888861
-
The genetically isolated populations of Finland and sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes.
Nat Genet. 2000 Jul;25(3):320-3
PMID: 10888882
-
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28.
Nat Genet. 2000 Jul;25(3):324-8
PMID: 10888883
-
Ancestral proportions and admixture dynamics in geographically defined African Americans living in South Carolina.
Am J Phys Anthropol. 2001 Jan;114(1):18-29
PMID: 11150049
-
Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations.
Ann Hum Genet. 2000 Mar;64(Pt 2):171-86
PMID: 11246470
-
Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci.
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9119-23
PMID: 3194414
-
The genetic structure of admixed populations.
Genetics. 1991 Feb;127(2):417-28
PMID: 2004712
-
Linkage disequilibrium in admixed populations: applications in gene mapping.
J Hered. 1994 Jan-Feb;85(1):59-63
PMID: 8120361
-
Mapping by admixture linkage disequilibrium in human populations: limits and guidelines.
Am J Hum Genet. 1994 Oct;55(4):809-24
PMID: 7942858
-
An E-M algorithm and testing strategy for multiple-locus haplotypes.
Am J Hum Genet. 1995 Mar;56(3):799-810
PMID: 7887436
-
The transmission/disequilibrium test: history, subdivision, and admixture.
Am J Hum Genet. 1995 Aug;57(2):455-64
PMID: 7668272
-
Ethnic-affiliation estimation by use of population-specific DNA markers.
Am J Hum Genet. 1997 Apr;60(4):957-64
PMID: 9106543
-
Genomewide transmission/disequilibrium testing--consideration of the genotypic relative risks at disease loci.
Am J Hum Genet. 1997 Dec;61(6):1424-30
PMID: 9399906
-
Mapping genes through the use of linkage disequilibrium generated by genetic drift: 'drift mapping' in small populations with no demographic expansion.
Hum Hered. 1998 May-Jun;48(3):138-54
PMID: 9618061
-
Mapping genes that underlie ethnic differences in disease risk: methods for detecting linkage in admixed populations, by conditioning on parental admixture.
Am J Hum Genet. 1998 Jul;63(1):241-51
PMID: 9634509
-
Mapping genes by drift-generated linkage disequilibrium.
Am J Hum Genet. 1998 Aug;63(2):654-6
PMID: 9683603
-
Estimating African American admixture proportions by use of population-specific alleles.
Am J Hum Genet. 1998 Dec;63(6):1839-51
PMID: 9837836
-
Linkage disequilibrium mapping of complex disease: fantasy or reality?
Curr Opin Biotechnol. 1998 Dec;9(6):578-94
PMID: 9889136
-
Use of unlinked genetic markers to detect population stratification in association studies.
Am J Hum Genet. 1999 Jul;65(1):220-8
PMID: 10364535
-
The future of genetic studies of complex human diseases.
Science. 1996 Sep 13;273(5281):1516-7
PMID: 8801636
-
Detection of the signature of natural selection in humans: evidence from the Duffy blood group locus.
Am J Hum Genet. 2000 May;66(5):1669-79
PMID: 10762551