Literature DB >> 20116045

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

Michael P Donnelly1, Peristera Paschou, Elena Grigorenko, David Gurwitz, Syed Qasim Mehdi, Sylvester L B Kajuna, Csaba Barta, Selemani Kungulilo, N J Karoma, Ru-Band Lu, Olga V Zhukova, Jong-Jin Kim, David Comas, Marcello Siniscalco, Maria New, Peining Li, Hui Li, Vangelis G Manolopoulos, William C Speed, Haseena Rajeevan, Andrew J Pakstis, Judith R Kidd, Kenneth K Kidd.   

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. Copyright (c) 2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20116045      PMCID: PMC2820164          DOI: 10.1016/j.ajhg.2010.01.007

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  29 in total

1.  The tau H2 haplotype is almost exclusively Caucasian in origin.

Authors:  Whitney Evans; Hon Chung Fung; John Steele; Johanna Eerola; Pentti Tienari; Alan Pittman; Rohan de Silva; Amanda Myers; Fabienne Wavrant-De Vrieze; Andrew Singleton; John Hardy
Journal:  Neurosci Lett       Date:  2004-10-21       Impact factor: 3.046

2.  A common inversion under selection in Europeans.

Authors:  Hreinn Stefansson; Agnar Helgason; Gudmar Thorleifsson; Valgerdur Steinthorsdottir; Gisli Masson; John Barnard; Adam Baker; Aslaug Jonasdottir; Andres Ingason; Vala G Gudnadottir; Natasa Desnica; Andrew Hicks; Arnaldur Gylfason; Daniel F Gudbjartsson; Gudrun M Jonsdottir; Jesus Sainz; Kari Agnarsson; Birgitta Birgisdottir; Shyamali Ghosh; Adalheidur Olafsdottir; Jean-Baptiste Cazier; Kristleifur Kristjansson; Michael L Frigge; Thorgeir E Thorgeirsson; Jeffrey R Gulcher; Augustine Kong; Kari Stefansson
Journal:  Nat Genet       Date:  2005-01-16       Impact factor: 38.330

3.  Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.

Authors:  J C Stephens; D E Reich; D B Goldstein; H D Shin; M W Smith; M Carrington; C Winkler; G A Huttley; R Allikmets; L Schriml; B Gerrard; M Malasky; M D Ramos; S Morlot; M Tzetis; C Oddoux; F S di Giovine; G Nasioulas; D Chandler; M Aseev; M Hanson; L Kalaydjieva; D Glavac; P Gasparini; E Kanavakis; M Claustres; M Kambouris; H Ostrer; G Duff; V Baranov; H Sibul; A Metspalu; D Goldman; N Martin; D Duffy; J Schmidtke; X Estivill; S J O'Brien; M Dean
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

4.  Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.

Authors:  M A Anderson; J F Gusella
Journal:  In Vitro       Date:  1984-11

5.  Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.

Authors:  Marc Cruts; Rosa Rademakers; Ilse Gijselinck; Julie van der Zee; Bart Dermaut; Tim de Pooter; Peter de Rijk; Jurgen Del-Favero; Christine van Broeckhoven
Journal:  Hum Mol Genet       Date:  2005-05-11       Impact factor: 6.150

6.  Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

Authors:  M Baker; I Litvan; H Houlden; J Adamson; D Dickson; J Perez-Tur; J Hardy; T Lynch; E Bigio; M Hutton
Journal:  Hum Mol Genet       Date:  1999-04       Impact factor: 6.150

7.  The architecture of the tau haplotype block in different ethnicities.

Authors:  Hon Chung Fung; Jessica Evans; Whitney Evans; Jaime Duckworth; Alan Pittman; Rohan de Silva; Amanda Myers; John Hardy
Journal:  Neurosci Lett       Date:  2004-12-22       Impact factor: 3.046

8.  Tau gene (MAPT) sequence variation among primates.

Authors:  Max Holzer; Molly Craxton; Ross Jakes; Thomas Arendt; Michel Goedert
Journal:  Gene       Date:  2004-10-27       Impact factor: 3.688

9.  Tau haplotypes regulate transcription and are associated with Parkinson's disease.

Authors:  John B J Kwok; Erdahl T Teber; Clement Loy; Marianne Hallupp; Garth Nicholson; George D Mellick; Daniel D Buchanan; Peter A Silburn; Peter R Schofield
Journal:  Ann Neurol       Date:  2004-03       Impact factor: 10.422

10.  The structure of the tau haplotype in controls and in progressive supranuclear palsy.

Authors:  Alan M Pittman; Amanda J Myers; Jaime Duckworth; Leslie Bryden; Melissa Hanson; Patrick Abou-Sleiman; Nicholas W Wood; John Hardy; Andrew Lees; Rohan de Silva
Journal:  Hum Mol Genet       Date:  2004-04-28       Impact factor: 6.150

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  30 in total

1.  Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs.

Authors:  Andrew J Pakstis; Rixun Fang; Manohar R Furtado; Judith R Kidd; Kenneth K Kidd
Journal:  Eur J Hum Genet       Date:  2012-04-25       Impact factor: 4.246

2.  Structural and functional characterization of H2 haplotype MAPT promoter: unique neurospecific domains and a hypoxia-inducible element would enhance rationally targeted tauopathy research for Alzheimer's disease.

Authors:  Bryan Maloney; Debomoy K Lahiri
Journal:  Gene       Date:  2012-01-30       Impact factor: 3.688

3.  Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

Authors:  Vladimir Vacic; Laurie J Ozelius; Lorraine N Clark; Anat Bar-Shira; Mali Gana-Weisz; Tanya Gurevich; Alexander Gusev; Merav Kedmi; Eimear E Kenny; Xinmin Liu; Helen Mejia-Santana; Anat Mirelman; Deborah Raymond; Rachel Saunders-Pullman; Robert J Desnick; Gil Atzmon; Edward R Burns; Harry Ostrer; Hakon Hakonarson; Aviv Bergman; Nir Barzilai; Ariel Darvasi; Inga Peter; Saurav Guha; Todd Lencz; Nir Giladi; Karen Marder; Itsik Pe'er; Susan B Bressman; Avi Orr-Urtreger
Journal:  Hum Mol Genet       Date:  2014-05-19       Impact factor: 6.150

4.  Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country.

Authors:  Miguel A Alfonso-Sánchez; Ibone Espinosa; Luis Gómez-Pérez; Alaitz Poveda; Esther Rebato; Jose A Peña
Journal:  Heredity (Edinb)       Date:  2017-12-11       Impact factor: 3.821

5.  Hunter-gatherer genomic diversity suggests a southern African origin for modern humans.

Authors:  Brenna M Henn; Christopher R Gignoux; Matthew Jobin; Julie M Granka; J M Macpherson; Jeffrey M Kidd; Laura Rodríguez-Botigué; Sohini Ramachandran; Lawrence Hon; Abra Brisbin; Alice A Lin; Peter A Underhill; David Comas; Kenneth K Kidd; Paul J Norman; Peter Parham; Carlos D Bustamante; Joanna L Mountain; Marcus W Feldman
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-07       Impact factor: 11.205

6.  Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.

Authors:  Farren B S Briggs; Selena E Bartlett; Benjamin A Goldstein; Joanne Wang; Jacob L McCauley; Rebecca L Zuvich; Philip L De Jager; John D Rioux; Adrian J Ivinson; Alastair Compston; David A Hafler; Stephen L Hauser; Jorge R Oksenberg; Stephen J Sawcer; Margaret A Pericak-Vance; Jonathan L Haines; Lisa F Barcellos
Journal:  Hum Mol Genet       Date:  2010-08-10       Impact factor: 6.150

7.  The microcephalin ancestral allele in a Neanderthal individual.

Authors:  Martina Lari; Ermanno Rizzi; Lucio Milani; Giorgio Corti; Carlotta Balsamo; Stefania Vai; Giulio Catalano; Elena Pilli; Laura Longo; Silvana Condemi; Paolo Giunti; Catherine Hänni; Gianluca De Bellis; Ludovic Orlando; Guido Barbujani; David Caramelli
Journal:  PLoS One       Date:  2010-05-14       Impact factor: 3.240

8.  Tau pathology: predictive diagnostics, targeted preventive and personalized medicine and application of advanced research in medical practice.

Authors:  Illana Gozes
Journal:  EPMA J       Date:  2010-06-12       Impact factor: 6.543

9.  Common variants at 6q22 and 17q21 are associated with intracranial volume.

Authors:  M Arfan Ikram; Myriam Fornage; Albert V Smith; Sudha Seshadri; Reinhold Schmidt; Stéphanie Debette; Henri A Vrooman; Sigurdur Sigurdsson; Stefan Ropele; H Rob Taal; Dennis O Mook-Kanamori; Laura H Coker; W T Longstreth; Wiro J Niessen; Anita L DeStefano; Alexa Beiser; Alex P Zijdenbos; Maksim Struchalin; Clifford R Jack; Fernando Rivadeneira; Andre G Uitterlinden; David S Knopman; Anna-Liisa Hartikainen; Craig E Pennell; Elisabeth Thiering; Eric A P Steegers; Hakon Hakonarson; Joachim Heinrich; Lyle J Palmer; Marjo-Riitta Jarvelin; Mark I McCarthy; Struan F A Grant; Beate St Pourcain; Nicholas J Timpson; George Davey Smith; Ulla Sovio; Mike A Nalls; Rhoda Au; Albert Hofman; Haukur Gudnason; Aad van der Lugt; Tamara B Harris; William M Meeks; Meike W Vernooij; Mark A van Buchem; Diane Catellier; Vincent W V Jaddoe; Vilmundur Gudnason; B Gwen Windham; Philip A Wolf; Cornelia M van Duijn; Thomas H Mosley; Helena Schmidt; Lenore J Launer; Monique M B Breteler; Charles DeCarli
Journal:  Nat Genet       Date:  2012-04-15       Impact factor: 38.330

10.  Structural diversity and African origin of the 17q21.31 inversion polymorphism.

Authors:  Karyn Meltz Steinberg; Francesca Antonacci; Peter H Sudmant; Jeffrey M Kidd; Catarina D Campbell; Laura Vives; Maika Malig; Laura Scheinfeldt; William Beggs; Muntaser Ibrahim; Godfrey Lema; Thomas B Nyambo; Sabah A Omar; Jean-Marie Bodo; Alain Froment; Michael P Donnelly; Kenneth K Kidd; Sarah A Tishkoff; Evan E Eichler
Journal:  Nat Genet       Date:  2012-07-01       Impact factor: 38.330

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