The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans

被引:54
作者
Donnelly, Michael P. [1 ]
Paschou, Peristera [4 ]
Grigorenko, Elena [2 ]
Gurwitz, David [5 ]
Mehdi, Syed Qasim [6 ]
Kajuna, Sylvester L. B. [7 ]
Barta, Csaba [8 ]
Kungulilo, Selemani [9 ]
Karoma, N. J. [7 ]
Lu, Ru-Band [10 ]
Zhukova, Olga V. [11 ]
Kim, Jong-Jin [12 ]
Comas, David [13 ,14 ]
Siniscalco, Marcello [15 ]
New, Maria [16 ]
Li, Peining [3 ]
Li, Hui [17 ,18 ,19 ]
Manolopoulos, Vangelis G. [20 ]
Speed, William C. [1 ]
Rajeevan, Haseena [1 ]
Pakstis, Andrew J. [1 ]
Kidd, Judith R. [1 ]
Kidd, Kenneth K. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Genet, Mol Cytogenet Lab, New Haven, CT 06520 USA
[4] Democritus Univ Thrace, Dept Mol Biol & Genet, Alexandropoulis 68100, Greece
[5] Tel Aviv Univ, Sackler Fac Med, Dept Human Mol Genet & Biochem, Natl Lab Genet Israeli Populat, IL-69978 Tel Aviv, Israel
[6] SIUT, Karachi 74200, Pakistan
[7] Hubert Kairuki Mem Univ, Dept Biochem & Mol Biol, Dar Es Salaam, Tanzania
[8] Semmelweis, Inst Med Chem Mol Biol & Pathobiochem, Budapest, Hungary
[9] Muhimbili Univ, Coll Hlth Sci, Dar Es Salaam, Tanzania
[10] Natl Cheng Kung Univ, Coll Med & Hosp, Dept Psychiat, Tainan 70101, Taiwan
[11] Russian Acad Sci, NI Vavilov Gen Genet Res Inst, Moscow, Russia
[12] Inst Nat Sci Invest, DNA Anal Div, Seoul, South Korea
[13] UPF, PRBB, Dept Expt & Hlth Sci, CSIC,Inst Evolutionary Biol, Barcelona 08003, Spain
[14] Ctr Invest Biomed Red CIBER Epidemiol & Salud Pub, Barcelona 08003, Spain
[15] Rockefeller Univ, Lab Stat Genet, New York, NY 10021 USA
[16] Mt Sinai Sch Med, New York, NY 10029 USA
[17] Fudan Univ, Key Lab Contemporary Anthropol, Minist Educ, Shanghai 200433, Peoples R China
[18] Fudan Univ, Sch Life Sci, Ctr Evolutionary Biol, Shanghai 200433, Peoples R China
[19] Fudan Univ, Inst Biomed Sci, Shanghai 200433, Peoples R China
[20] Democritus Univ Thrace, Sch Med, Pharmacol Lab, Alexandroupolis 68100, Greece
基金
美国国家卫生研究院;
关键词
PROGRESSIVE SUPRANUCLEAR PALSY; POPULATION GENOTYPE DATA; H2 MAPT HAPLOTYPE; FRONTOTEMPORAL DEMENTIA; PARKINSONS-DISEASE; TAU HAPLOTYPE; HUMAN GENOME; ARCHITECTURE; ASSOCIATION; H1;
D O I
10.1016/j.ajhg.2010.01.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The polymorphic inversion on 17q21, sometimes called the microtubular associated protein tau (MAPT) inversion, is an similar to 900 kb inversion found primarily in Europeans and Southwest Asians. We have identified 21. SNPs that act as markers of the inverted, i.e., H2, haplotype. The inversion is found at the highest frequencies in Southwest Asia and Southern Europe (frequencies of similar to 30%); elsewhere in Europe, frequencies vary from <5%, in Finns, to 28%, in Orcadians. The H2 inversion haplotype also Occurs at low frequencies in Africa, Central Asia, East Asia, and the Americas, though the East Asian and Amerindian alleles may be due to recent gene flow from Europe. Molecular evolution analyses indicate that the H2 haplotype originally arose in Africa or Southwest Asia. Though the H2 inversion has many fixed differences across the similar to 900 kb, short tandem repeat polymorphism data indicate a very recent date for the most recent common ancestor, with dates ranging from 13,600 to 108,400 years, depending on assumptions and estimation methods. This estimate range is much more recent than the 3 million year age estimated by Stefansson et al. in 2005.(1)
引用
收藏
页码:161 / 171
页数:11
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