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Proportionally more deleterious genetic variation in European than in African populations.

Proportionally more deleterious genetic variation in European than in African populations. Research Abstract Details 

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  • Proportionally more deleterious genetic variation in European than in African populations. Abstract Text:

    kirk e lohmuellerKirk E Lohmueller,amit r indapAmit R Indap,steffen schmidtSteffen Schmidt,adam r boykoAdam R Boyko,ryan d hernandezRyan D Hernandez,melissa j hubiszMelissa J Hubisz,john j sninskyJohn J Sninsky,thomas j whiteThomas J White,shamil r sunyaevShamil R Sunyaev,rasmus nielsenRasmus Nielsen,andrew g clarkAndrew G Clark,carlos d bustamanteCarlos D Bustamante,kirk e lohmuellerKirk E Lohmueller,amit r indapAmit R Indap,steffen schmidtSteffen Schmidt,adam r boykoAdam R Boyko,ryan d hernandezRyan D Hernandez,melissa j hubiszMelissa J Hubisz,john j sninskyJohn J Sninsky,thomas j whiteThomas J White,shamil r sunyaevShamil R Sunyaev,rasmus nielsenRasmus Nielsen,andrew g clarkAndrew G Clark,carlos d bustamanteCarlos D Bustamante,

    Quantifying the number of deleterious mutations per diploid human genome is of crucial concern to both evolutionary and medical geneticists. Here we combine genome-wide polymorphism data from PCR-based exon resequencing, comparative genomic data across mammalian species, and protein structure predictions to estimate the number of functionally consequential single-nucleotide polymorphisms (SNPs) carried by each of 15 African American (AA) and 20 European American (EA) individuals. We find that AAs show significantly higher levels of nucleotide heterozygosity than do EAs for all categories of functional SNPs considered, including synonymous, non-synonymous, predicted 'benign', predicted 'possibly damaging' and predicted 'probably damaging' SNPs. This result is wholly consistent with previous work showing higher overall levels of nucleotide variation in African populations than in Europeans. EA individuals, in contrast, have significantly more genotypes homozygous for the derived allele at synonymous and non-synonymous SNPs and for the damaging allele at 'probably damaging' SNPs than AAs do. For SNPs segregating only in one population or the other, the proportion of non-synonymous SNPs is significantly higher in the EA sample (55.4%) than in the AA sample (47.0%; P < 2.3 x 10(-37)). We observe a similar proportional excess of SNPs that are inferred to be 'probably damaging' (15.9% in EA; 12.1% in AA; P < 3.3 x 10(-11)). Using extensive simulations, we show that this excess proportion of segregating damaging alleles in Europeans is probably a consequence of a bottleneck that Europeans experienced at about the time of the migration out of Africa.

    Proportionally more deleterious genetic variation in European than in African populations. Publishing Authors By Initials

    ke lohmuellerKE Lohmueller,ar indapAR Indap,s schmidtS Schmidt,ar boykoAR Boyko,rd hernandezRD Hernandez,mj hubiszMJ Hubisz,jj sninskyJJ Sninsky,tj whiteTJ White,sr sunyaevSR Sunyaev,r nielsenR Nielsen,ag clarkAG Clark,cd bustamanteCD Bustamante,ke lohmuellerKE Lohmueller,ar indapAR Indap,s schmidtS Schmidt,ar boykoAR Boyko,rd hernandezRD Hernandez,mj hubiszMJ Hubisz,jj sninskyJJ Sninsky,tj whiteTJ White,sr sunyaevSR Sunyaev,r nielsenR Nielsen,ag clarkAG Clark,cd bustamanteCD Bustamante,

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    Proportionally more deleterious genetic variation in European than in African populations. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Nature

    VOLUME: 451

    Page Numbers: 994-7

    Journal Abbreviation: Nature

    ISSN: 1476-4687

    DAY: 21

    MONTH: Feb

    YEAR: 2008

    Proportionally more deleterious genetic variation in European than in African populations. Information

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    LANGUAGE: eng

    NlmUniqueID: 410462

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    Grant and Affiliation Information for Proportionally more deleterious genetic variation in European than in African populations.

    AFFILIATION: Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853, USA.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Nature

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