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
References (29)
29 references, click to expand
-
The structure of the tau haplotype in controls and in progressive supranuclear palsy.
Hum Mol Genet. 2004 Jun 15;13(12):1267-74
PMID: 15115761
-
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts.
Neurobiol Dis. 2007 Mar;25(3):561-70
PMID: 17174556
-
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
Hum Mol Genet. 2005 Jul 1;14(13):1753-62
PMID: 15888485
-
Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
Am J Hum Genet. 2004 Oct;75(4):669-77
PMID: 15297935
-
A new statistical method for haplotype reconstruction from population data.
Am J Hum Genet. 2001 Apr;68(4):978-89
PMID: 11254454
-
Tau-mediated neurodegeneration in Alzheimer's disease and related disorders.
Nat Rev Neurosci. 2007 Sep;8(9):663-72
PMID: 17684513
-
Evolutionary toggling of the MAPT 17q21.31 inversion region.
Nat Genet. 2008 Sep;40(9):1076-83
PMID: 19165922
-
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase.
Am J Hum Genet. 2006 Apr;78(4):629-44
PMID: 16532393
-
Tau haplotypes regulate transcription and are associated with Parkinson's disease.
Ann Neurol. 2004 Mar;55(3):329-34
PMID: 14991810
-
The tau H2 haplotype is almost exclusively Caucasian in origin.
Neurosci Lett. 2004 Oct 21;369(3):183-5
PMID: 15464261
-
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
Nat Genet. 2006 Sep;38(9):1038-42
PMID: 16906162
-
Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.
DNA Seq. 1998;8(5):317-27
PMID: 10993602
-
A common inversion under selection in Europeans.
Nat Genet. 2005 Feb;37(2):129-37
PMID: 15654335
-
Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens.
Biochem Soc Trans. 2005 Aug;33(Pt 4):582-5
PMID: 16042549
-
Genotype, haplotype and copy-number variation in worldwide human populations.
Nature. 2008 Feb 21;451(7181):998-1003
PMID: 18288195
-
Further extension of the H1 haplotype associated with progressive supranuclear palsy.
Mov Disord. 2002 May;17(3):550-6
PMID: 12112206
-
Tau gene (MAPT) sequence variation among primates.
Gene. 2004 Oct 27;341:313-22
PMID: 15474313
-
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.
Am J Hum Genet. 1998 Jun;62(6):1507-15
PMID: 9585595
-
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.
Nat Genet. 2006 Sep;38(9):1032-7
PMID: 16906163
-
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
Nat Genet. 2006 Sep;38(9):999-1001
PMID: 16906164
-
Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.
In Vitro. 1984 Nov;20(11):856-8
PMID: 6519667
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy.
Hum Mol Genet. 1999 Apr;8(4):711-5
PMID: 10072441
-
The architecture of the tau haplotype block in different ethnicities.
Neurosci Lett. 2005 Mar 29;377(2):81-4
PMID: 15740841
-
Worldwide human relationships inferred from genome-wide patterns of variation.
Science. 2008 Feb 22;319(5866):1100-4
PMID: 18292342
-
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease.
Eur J Hum Genet. 2007 Nov;15(11):1163-8
PMID: 17637803
-
The H2 MAPT haplotype is associated with familial frontotemporal dementia.
Neurobiol Dis. 2006 May;22(2):357-62
PMID: 16410051
-
Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients.
Hum Mutat. 2006 Oct;27(10):1057-9
PMID: 16906510
-
Standardized subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, accounting for atypical and duplicated samples and pairs of close relatives.
Ann Hum Genet. 2006 Nov;70(Pt 6):841-7
PMID: 17044859
-
A comparison of bayesian methods for haplotype reconstruction from population genotype data.
Am J Hum Genet. 2003 Nov;73(5):1162-9
PMID: 14574645