Positive Selection on the Osteoarthritis-Risk and Decreased-Height Associated Variants at the GDF5 Gene in East Asians

被引:21
作者
Wu, Dong-Dong [1 ]
Li, Gui-Mei [2 ]
Jin, Wei [2 ]
Li, Yan [1 ]
Zhang, Ya-Ping [1 ,2 ]
机构
[1] Chinese Acad Sci, Kunming Inst Zool, State Key Lab Genet Resources & Evolut, Kunming, Peoples R China
[2] Yunnan Univ, Lab Conservat & Utilizat Bioresource, Kunming, Peoples R China
基金
中国国家自然科学基金;
关键词
HUMAN GENOME; POPULATION DIFFERENTIATION; HAPLOTYPE RECONSTRUCTION; STATISTICAL-METHOD; NATURAL-SELECTION; BODY-SIZE; MUTATION; SUSCEPTIBILITY; SNP; POLYMORPHISM;
D O I
10.1371/journal.pone.0042553
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
GDF5 is a member of the bone morphogenetic protein (BMP) gene family, and plays an important role in the development of the skeletal system. Variants of the gene are associated with osteoarthritis and height in some human populations. Here, we resequenced the gene in individuals from four geographically separated human populations, and found that the evolution of the promoter region deviated from neutral expectations, with the sequence evolution driven by positive selection in the East Asian population, especially the haplotypes carrying the derived alleles of 5' UTR SNPs rs143384 and rs143383. The derived alleles of rs143384 and rs143383, which are associated with a risk of osteoarthritis and decreased height, have high frequencies in non-Africans and show strong extended haplotype homozygosity and high population differentiation in East Asian. It is concluded that positive selection has driven the rapid evolution of the two osteoarthritis osteoarthritis-risk and decreased height associated variants of the human GDF5 gene, and supports the suggestion that the reduction in body size during the terminal Pleistocene and Holocene period might have been an adaptive process influenced by genetic factors.
引用
收藏
页数:9
相关论文
共 46 条
[1]   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
[2]  
[Anonymous], ARXIV11025604V1
[3]   Signatures of natural selection in the human genome [J].
Bamshad, M ;
Wooding, SP .
NATURE REVIEWS GENETICS, 2003, 4 (02) :99-111A
[4]   Median-joining networks for inferring intraspecific phylogenies [J].
Bandelt, HJ ;
Forster, P ;
Röhl, A .
MOLECULAR BIOLOGY AND EVOLUTION, 1999, 16 (01) :37-48
[5]  
Cann HM, 2002, SCIENCE, V296, P261
[6]  
CHANG SC, 1994, J BIOL CHEM, V269, P28227
[7]   A meta-analysis of European and Asian cohorts reveals a global role of a functional SNP in the 5′ UTR of GDF5 with osteoarthritis susceptibility [J].
Chapman, Kay ;
Takahashi, Atsushi ;
Meulenbelt, Ingrid ;
Watson, Chris ;
Rodriguez-Lopez, Julio ;
Egli, Rainer ;
Tsezou, Aspasia ;
Malizos, Konstantinos N. ;
Kloppenburg, Margreet ;
Shi, Dongquan ;
Southam, Lorraine ;
van der Breggen, Ruud ;
Donn, Rachelle ;
Qin, Jianghui ;
Doherty, Michael ;
Slagboom, P. Eline ;
Wallis, Gillian ;
Kamatani, Naoyuki ;
Jiang, Qing ;
Gonzalez, Antonio ;
Loughlin, John ;
Ikegawa, Shiro .
HUMAN MOLECULAR GENETICS, 2008, 17 (10) :1497-1504
[8]   Evidence of positive selection acting at the human dopamine receptor D4 gene locus [J].
Ding, YC ;
Chi, HC ;
Grady, DL ;
Morishima, A ;
Kidd, JR ;
Kidd, KK ;
Flodman, P ;
Spence, MA ;
Schuck, S ;
Swanson, JM ;
Zhang, YP ;
Moyzis, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :309-314
[9]   Functional Analysis of the Osteoarthritis Susceptibility-Associated GDF5 Regulatory Polymorphism [J].
Egli, Rainer J. ;
Southam, Lorraine ;
Wilkins, James M. ;
Lorenzen, Inken ;
Pombo-Suarez, Manuel ;
Gonzalez, Antonio ;
Carr, Andrew ;
Chapman, Kay ;
Loughlin, John .
ARTHRITIS AND RHEUMATISM, 2009, 60 (07) :2055-2064
[10]   Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome) [J].
Faiyaz-Ul-Haque, M ;
Ahmad, W ;
Zaidi, SHE ;
Haque, S ;
Teebi, AS ;
Ahmad, M ;
Cohn, DH ;
Tsui, LC .
CLINICAL GENETICS, 2002, 61 (06) :454-458