The case for selection at CCR5-Δ32

被引:152
作者
Sabeti, PC
Walsh, E
Schaffner, SF
Varilly, P
Fry, B
Hutcheson, HB
Cullen, M
Mikkelsen, TS
Roy, J
Patterson, N
Cooper, R
Reich, D
Altshuler, D
O'Brien, S
Lander, ES
机构
[1] MIT, Broad Inst, Cambridge, MA 02139 USA
[2] Harvard Univ, Cambridge, MA 02138 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[4] NCI, Lab Genom Divers, Frederick, MD 21701 USA
[5] Loyola Univ, Sch Med, Dept Epidemiol & Prevent Med, Maywood, IL 60153 USA
[6] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[7] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[8] Massachusetts Gen Hosp, Dept Med, Diabet Unit, Ctr Human Genet Res, Boston, MA 02114 USA
[9] MIT, Dept Biol, Cambridge, MA USA
[10] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[11] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA
关键词
D O I
10.1371/journal.pbio.0030378
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1963 / 1969
页数:7
相关论文
共 32 条
[1]   Population history and natural selection shape patterns of genetic variation in 132 genes [J].
Akey, JM ;
Eberle, MA ;
Rieder, MJ ;
Carlson, CS ;
Shriver, MD ;
Nickerson, DA ;
Kruglyak, L .
PLOS BIOLOGY, 2004, 2 (10) :1591-1599
[2]   Interrogating a high-density SNP map for signatures of natural selection [J].
Akey, JM ;
Zhang, G ;
Zhang, K ;
Jin, L ;
Shriver, MD .
GENOME RESEARCH, 2002, 12 (12) :1805-1814
[3]   Signatures of natural selection in the human genome [J].
Bamshad, M ;
Wooding, SP .
NATURE REVIEWS GENETICS, 2003, 4 (02) :99-111A
[4]   A strong signature of balancing selection in the 5′ cis-regulatory region of CCR5 [J].
Bamshad, MJ ;
Mummidi, S ;
Gonzalez, E ;
Ahuja, SS ;
Dunn, DM ;
Watkins, WS ;
Wooding, S ;
Stone, AC ;
Jorde, LB ;
Weiss, RB ;
Ahuja, SK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10539-10544
[5]  
Carr E. G., 1999, J POSIT BEHAV INTERV, V1, P5, DOI DOI 10.1177/109830079900100103
[6]   Novel alleles of the chemokine-receptor gene CCR5 [J].
Carrington, M ;
Kissner, T ;
Gerrard, B ;
Ivanov, S ;
O'Brien, SJ ;
Dean, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (06) :1261-1267
[7]   Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene [J].
Dean, M ;
Carrington, M ;
Winkler, C ;
Huttley, GA ;
Smith, MW ;
Allikmets, R ;
Goedert, JJ ;
Buchbinder, SP ;
Vittinghoff, E ;
Gomperts, E ;
Donfield, S ;
Vlahov, D ;
Kaslow, R ;
Saah, A ;
Rinaldo, C ;
Detels, R ;
OBrien, SJ .
SCIENCE, 1996, 273 (5283) :1856-1862
[8]   Reappraisal of the historical selective pressures for the CCR5-Δ32 mutation [J].
Duncan, SR ;
Scott, S ;
Duncan, CJ .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (03) :205-208
[9]  
Fay JC, 2000, GENETICS, V155, P1405
[10]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229