Three Novel mtDNA Restriction Site Polymorphisms Allow Exploration of Population Affinities of African Americans

2003 
1 Abstract To develop informative tools for the study of population affini- ties in African Americans, we sequenced the hypervariable segments I and II (HVS I and HVS II) of mitochondrial DNA (mtDNA) from 96 Sierra Leoneans; European Americans; rural, Gullah-speaking African Americans; urban African Americans living in Charleston, South Carolina; and Ja- maicans. We identified single nucleotide polymorphisms (SNPs) exhibiting ethnic affinities, and developed restriction endonuclease tools to screen these SNPs. Here we show that three HVS restriction site polymorphisms (RSPs), EcoRV, Fok I, and MfeI, exhibit appreciable differences in frequency (average δ = 0.4165) between putative African American parental populations (i.e., ex- tant Africans living in Sierra Leone and European Americans). Estimates of European American mtDNA admixture, calculated from haplotypes com- posed of these three novel RSPs, show a cline of increasing admixture from Gullah-speaking African American (m = 0.0300) to urban Charleston African American (m = 0.0689) to West Coast African American (m = 0.1769) popu- lations. This haplotype admixture in the Gullahs is the lowest recorded to date among African Americans, consistent with previous studies using auto- somal markers. These RSPs may become valuable new tools in the study of ancestral affinities and admixture dynamics of African Americans. As sequencing efforts for the human genome near completion, interest is increas- ing in genetic diversity. Of particular interest to population geneticists are poly- morphisms that vary predictably within and between populations. Mitochondrial DNA (mtDNA), specifically the hypervariable segments I and II (HVS I and HVS II) of the D-loop, has several general features that make it valuable for studying
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    23
    References
    33
    Citations
    NaN
    KQI
    []