X-chromosomal genetic diversity and linkage disequilibrium patterns in Amerindians and non-Amerindian populations

Authors

  • Carlos Eduardo G. Amorim,

    1. Programa de Pós-Graduação em Genética e Biologia Molecular and Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501-970, Porto Alegre, RS, Brazil
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  • Sijia Wang,

    1. The Galton Laboratory, Department of Biology, University College London, London, United Kingdom
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  • Andrea R. Marrero,

    1. Programa de Pós-Graduação em Genética e Biologia Molecular and Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501-970, Porto Alegre, RS, Brazil
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  • Francisco M. Salzano,

    1. Programa de Pós-Graduação em Genética e Biologia Molecular and Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501-970, Porto Alegre, RS, Brazil
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  • Andrés Ruiz-Linares,

    1. The Galton Laboratory, Department of Biology, University College London, London, United Kingdom
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  • Maria Cátira Bortolini

    Corresponding author
    1. Programa de Pós-Graduação em Genética e Biologia Molecular and Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501-970, Porto Alegre, RS, Brazil
    • Programa de Pós-Graduação em Genética e Biologia Molecular and Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Caixa Postal 15053, 91501-970, Porto Alegre, RS, Brazil
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Abstract

Objectives: We report X-chromosomal linkage disequilibrium (LD) patterns in Amerindian (Kogi, Wayuu, and Zenu) and admixed Latin American (Central Valley of Costa Rica and Southern Brazilian Gaucho) populations.

Methods: Short tandem repeats (STRs) widespread along the X-chromosome were investigated in 132 and 124 chromosomes sampled from the Amerindian tribes and the admixed Latin American populations, respectively. Diversity indexes (gene diversity and average numbers of alleles per locus) were estimated for each population and the level of LD was inferred with an exact test.

Results: The Amerindian populations presented lower genetic diversity and a higher proportion of loci in LD than the admixed ones. Two haplotype blocks were identified in the X-chromosome, both restricted to the Amerindians. The first involved DXS8051 and DXS7108 in Xp22.22 and Xp22.3, while the second found only among the Kogi, included eight loci in a region between Xp11.4 and Xq21.1.

Conclusions: In accordance to previous work done with other populations, human isolates, such as Amerindian tribes, seem to be an optimal choice for the implementation of association studies due to the wide extent of LD which can be found in their gene pool. On the other hand, the low proportion of loci in LD found in both admixed populations studied here could be explained by events related to their history and similarities between the allele frequencies in the parental stocks. Am. J. Hum. Biol., 2011. © 2011 Wiley-Liss, Inc.

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