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PMID: 20116045 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

The distribution and most recent common ancestor of the 17q21 inversion in humans.

American journal of human genetics ·Vol. 86 ·No. 2 ·2010-02-12 ·Pages 161-71

Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK

Abstract

The polymorphic inversion on 17q21, sometimes called the microtubular associated protein tau (MAPT) inversion, is an approximately 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 approximately 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 approximately 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.

MeSH Terms
Animals Chromosome Inversion/genetics Chromosomes, Human, Pair 17/genetics Heterozygote Humans In Situ Hybridization, Fluorescence Ireland Microsatellite Repeats/genetics Phylogeny Polymorphism, Single Nucleotide/genetics Primates/genetics
Authors & Affiliations
23 authors, click to expand affiliations / ORCID
Donnelly Michael P
Department of Genetics, School of Medicine, Yale University, New Haven, CT 06520, USA.
Paschou Peristera
Grigorenko Elena
Gurwitz David
Mehdi Syed Qasim
Kajuna Sylvester L B
Barta Csaba
Kungulilo Selemani
Karoma N J
Lu Ru-Band
Zhukova Olga V
Kim Jong-Jin
Comas David
Siniscalco Marcello
New Maria
Li Peining
Li Hui
Manolopoulos Vangelis G
Speed William C
Rajeevan Haseena
Pakstis Andrew J
Kidd Judith R
Kidd Kenneth K
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
1537-6605
Published
2010-02-12
Epub
2010-00-28
Pages
161-71
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC2820164
Subset
IM
Grants
NIGMS NIH HHS · P01 GM057672 · United States
NIGMS NIH HHS · GM57672 · United States
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