A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia

被引:53
作者
Hardwick, Robert J. [1 ]
Machado, Lee R. [1 ]
Zuccherato, Luciana W. [2 ]
Antolinos, Suzanne [1 ]
Xue, Yali [3 ]
Shawa, Nyambura [4 ,5 ]
Gilman, Robert H. [6 ,7 ]
Cabrera, Lilia [7 ]
Berg, Douglas E. [8 ]
Tyler-Smith, Chris [3 ]
Kelly, Paul [4 ,5 ]
Tarazona-Santos, Eduardo [2 ]
Hollox, Edward J. [1 ]
机构
[1] Univ Leicester, Dept Genet, Leicester LE1 7RH, Leics, England
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Biol Geral, Belo Horizonte, MG, Brazil
[3] Wellcome Trust Sanger Inst, Hinxton, S Cambs, England
[4] Univ Zambia, Sch Med, Trop Gastroenterol & Nutr Grp, Lusaka, Zambia
[5] Queen Mary Univ London, Barts & London Sch Med, Inst Cell & Mol Sci, London, England
[6] Johns Hopkins Univ, Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[7] Ascociac Benef PRISMA, Lima, Peru
[8] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
基金
英国医学研究理事会; 英国惠康基金; 美国国家卫生研究院;
关键词
CNV; defensin; antimicrobial; influenza; paralogue ratio test; HUMAN BETA-DEFENSIN-3; EVOLUTION; GENOME; POLYMORPHISM; DIVERSITY; DUPLICATIONS; LOCUS; COALESCENT; PSORIASIS; INVERSION;
D O I
10.1002/humu.21491
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Beta-defensins are a family of multifunctional genes with roles in defense against pathogens, reproduction, and pigmentation. In humans, six beta-defensin genes are clustered in a repeated region which is copy-number variable (CNV) as a block, with a diploid copy number between 1 and 12. The role in host defense makes the evolutionary history of this CNV particularly interesting, because morbidity due to infectious disease is likely to have been an important selective force in human evolution, and to have varied between geographical locations. Here, we show CNV of the beta-defensin region in chimpanzees, and identify a beta-defensin block in the human lineage that contains rapidly evolving noncoding regulatory sequences. We also show that variation at one of these rapidly evolving sequences affects expression levels and cytokine responsiveness of DEFB103, a key inhibitor of influenza virus fusion at the cell surface. A worldwide analysis of beta-defensin CNV in 67 populations shows an unusually high frequency of high-DEFB103-expressing copies in East Asia, the geographical origin of historical and modern influenza epidemics, possibly as a result of selection for increased resistance to influenza in this region. Hum Mutat 32:743-750, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:743 / 750
页数:8
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