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The case for selection at CCR5-Delta 32

  1. Author:
    Sabeti, P. C.
    Walsh, E.
    Schaffner, S. F.
    Varilly, P.
    Fry, B.
    Hutcheson, H. B.
    Cullen, M.
    Mikkelsen, T. S.
    Roy, J.
    Patterson, N.
    Cooper, R.
    Reich, D.
    Altshuler, D.
    O'Brien, S.
    Lander, E. S.
  2. Author Address

    MIT, Broad Inst, Cambridge, MA 02139 USA. Harvard Univ, Cambridge, MA 02138 USA. Harvard Univ, Sch Med, Dept Genet, Boston, MA USA. NCI, Lab Genom Divers, Frederick, MD 21701 USA. Loyola Univ, Sch Med, Dept Epidemiol & Prevent Med, Maywood, IL 60153 USA. Harvard Univ, Sch Med, Dept Med, Boston, MA USA. Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA. Massachusetts Gen Hosp, Dept Med, Diabet Unit, Ctr Human Genet Res, Boston, MA 02114 USA. MIT, Dept Biol, Cambridge, MA USA. Whitehead Inst Biomed Res, Cambridge, MA 02142 USA. Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA Sabeti, PC, MIT, Broad Inst, 77 Massachusetts Ave, Cambridge, MA 02139 USA
    1. Year: 2005
    2. Date: NOV
  1. Journal: Plos Biology
    1. 3
    2. 11
    3. Pages: 1963-1969
  2. Type of Article: Article
  1. Abstract:

    The C-C chemokine receptor 5, 32 base-pair deletion (CCR5-Delta 32) allele confers strong resistance to infection by the AIDS virus HIV. Previous studies have suggested that CCR5-Delta 32 arose within the past 1,000 y and rose to its present high frequency (5% - 14%) in Europe as a result of strong positive selection, perhaps by such selective agents as the bubonic plague or smallpox during the Middle Ages. This hypothesis was based on several lines of evidence, including the absence of the allele outside of Europe and long-range linkage disequilibrium at the locus. We reevaluated this evidence with the benefit of much denser genetic maps and extensive control data. We find that the pattern of genetic variation at CCR5-Delta 32 does not stand out as exceptional relative to other loci across the genome. Moreover using newer genetic maps, we estimated that the CCR5-Delta 32 allele is likely to have arisen more than 5,000 y ago. While such results can not rule out the possibility that some selection may have occurred at C-C chemokine receptor 5 (CCR5), they imply that the pattern of genetic variation seen at CCR5-Delta 32 is consistent with neutral evolution. More broadly, the results have general implications for the design of future studies to detect the signs of positive selection in the human genome

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External Sources

  1. WOS: 000233609300015

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