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      History Shaped the Geographic Distribution of Genomic Admixture on the Island of Puerto Rico

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          Abstract

          Contemporary genetic variation among Latin Americans human groups reflects population migrations shaped by complex historical, social and economic factors. Consequently, admixture patterns may vary by geographic regions ranging from countries to neighborhoods. We examined the geographic variation of admixture across the island of Puerto Rico and the degree to which it could be explained by historic and social events. We analyzed a census-based sample of 642 Puerto Rican individuals that were genotyped for 93 ancestry informative markers (AIMs) to estimate African, European and Native American ancestry. Socioeconomic status (SES) data and geographic location were obtained for each individual. There was significant geographic variation of ancestry across the island. In particular, African ancestry demonstrated a decreasing East to West gradient that was partially explained by historical factors linked to the colonial sugar plantation system. SES also demonstrated a parallel decreasing cline from East to West. However, at a local level, SES and African ancestry were negatively correlated. European ancestry was strongly negatively correlated with African ancestry and therefore showed patterns complementary to African ancestry. By contrast, Native American ancestry showed little variation across the island and across individuals and appears to have played little social role historically. The observed geographic distributions of SES and genetic variation relate to historical social events and mating patterns, and have substantial implications for the design of studies in the recently admixed Puerto Rican population. More generally, our results demonstrate the importance of incorporating social and geographic data with genetics when studying contemporary admixed populations.

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          Mapping human genetic diversity in Asia.

          Asia harbors substantial cultural and linguistic diversity, but the geographic structure of genetic variation across the continent remains enigmatic. Here we report a large-scale survey of autosomal variation from a broad geographic sample of Asian human populations. Our results show that genetic ancestry is strongly correlated with linguistic affiliations as well as geography. Most populations show relatedness within ethnic/linguistic groups, despite prevalent gene flow among populations. More than 90% of East Asian (EA) haplotypes could be found in either Southeast Asian (SEA) or Central-South Asian (CSA) populations and show clinal structure with haplotype diversity decreasing from south to north. Furthermore, 50% of EA haplotypes were found in SEA only and 5% were found in CSA only, indicating that SEA was a major geographic source of EA populations.
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            Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico.

            Mexico is developing the basis for genomic medicine to improve healthcare of its population. The extensive study of genetic diversity and linkage disequilibrium structure of different populations has made it possible to develop tagging and imputation strategies to comprehensively analyze common genetic variation in association studies of complex diseases. We assessed the benefit of a Mexican haplotype map to improve identification of genes related to common diseases in the Mexican population. We evaluated genetic diversity, linkage disequilibrium patterns, and extent of haplotype sharing using genomewide data from Mexican Mestizos from regions with different histories of admixture and particular population dynamics. Ancestry was evaluated by including 1 Mexican Amerindian group and data from the HapMap. Our results provide evidence of genetic differences between Mexican subpopulations that should be considered in the design and analysis of association studies of complex diseases. In addition, these results support the notion that a haplotype map of the Mexican Mestizo population can reduce the number of tag SNPs required to characterize common genetic variation in this population. This is one of the first genomewide genotyping efforts of a recently admixed population in Latin America.
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              Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups.

              Information on the prevalence of pathogenic BRCA1 mutation carriers in racial/ethnic minority populations is limited. To estimate BRCA1 carrier prevalence in Hispanic, African American, and Asian American female breast cancer patients compared with non-Hispanic white patients with and without Ashkenazi Jewish ancestry. We estimated race/ethnicity-specific prevalence of BRCA1 in a population-based, multiethnic series of female breast cancer patients younger than 65 years at diagnosis who were enrolled at the Northern California site of the Breast Cancer Family Registry during the period 1996-2005. Race/ethnicity and religious ancestry were based on self-report. Weighted estimates of prevalence and 95% confidence intervals (CIs) were based on Horvitz-Thompson estimating equations. Estimates of BRCA1 prevalence. Estimates of BRCA1 prevalence were 3.5% (95% CI, 2.1%-5.8%) in Hispanic patients (n = 393), 1.3% (95% CI, 0.6%-2.6%) in African American patients (n = 341), and 0.5% (95% CI, 0.1%-2.0%) in Asian American patients (n = 444), compared with 8.3% (95% CI, 3.1%-20.1%) in Ashkenazi Jewish patients (n = 41) and 2.2% (95% CI, 0.7%-6.9%) in other non-Hispanic white patients (n = 508). Prevalence was particularly high in young (<35 years) African American patients (5/30 patients [16.7%]; 95% CI, 7.1%-34.3%). 185delAG was the most common mutation in Hispanics, found in 5 of 21 carriers (24%). Among African American, Asian American, and Hispanic patients in the Northern California Breast Cancer Family Registry, the prevalence of BRCA1 mutation carriers was highest in Hispanics and lowest in Asian Americans. The higher carrier prevalence in Hispanics may reflect the presence of unrecognized Jewish ancestry in this population.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                31 January 2011
                : 6
                : 1
                : e16513
                Affiliations
                [1 ]Department of Medicine, University of California San Francisco, San Francisco, California, United States of America
                [2 ]Institute for Human Genetics, University of California, San Francisco, California, United States of America
                [3 ]Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California, United States of America
                [4 ]Department of Urology, University of California San Francisco, San Francisco, California, United States of America
                [5 ]Department of Biology, University of Puerto Rico, Mayagüez, Puerto Rico
                [6 ]Department of Biology, University of Puerto Rico, Río Piedras, Puerto Rico
                [7 ]Department of Genetics, Cell Biology & Developmental Biology, University of Minnesota, Minneapolis, Minnesota, United States of America
                [8 ]Division of Research, Kaiser Permanente, Oakland, California, United States of America
                [9 ]Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America
                State University of New York College at Oneonta, United States of America
                Author notes

                Conceived and designed the experiments: MV CRG LF EZ NR EGB JCM-C. Performed the experiments: MV KB. Analyzed the data: MV CRG LAR JG SC NR JCM-C. Contributed reagents/materials/analysis tools: GT-L JV-V KB JCM-C. Wrote the paper: MV CRG LAR LF JG TKO EZ NR EGB JCM-C.

                [¤]

                Current address: Laboratory of Anthropology, Department of Animal Biology, University of Barcelona, Barcelona, Spain

                Article
                PONE-D-10-03795
                10.1371/journal.pone.0016513
                3031579
                21304981
                a499add1-9d2f-47eb-931d-6c6355123766
                Via et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 19 October 2010
                : 4 January 2011
                Page count
                Pages: 8
                Categories
                Research Article
                Biology
                Evolutionary Biology
                Evolutionary Processes
                Hybridization
                Population Genetics
                Gene Flow
                Genetic Polymorphism
                Genetics
                Heredity
                Genotypes
                Human Genetics
                Computer Science
                Geoinformatics
                Earth Sciences
                Geography
                Geoinformatics
                Human Geography
                Social and Behavioral Sciences
                Anthropology
                Cultural Anthropology
                Ethnic Groups
                Biological Anthropology
                Ethnobiology
                Physical Anthropology
                Social Anthropology
                Geography
                Geoinformatics
                Human Geography
                Sociology
                Demography
                Ethnic Groups

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