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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Authors :
Laura J. Scott
Neil Robertson
Anders Hamsten
Domenico Palli
Susanne Moebus
Bernhard O. Boehm
Gunnar Sigurðsson
Paul W. Franks
C. N. A. Palmer
Sonali Pechlivanis
Katharine R. Owen
Michael E. Reschen
Sarah Edkins
Jason Carey
Christopher A. O’Callaghan
Norman Klopp
Caroline S. Fox
Petter Storm
N. William Rayner
Johan G. Eriksson
Thomas Illig
Anubha Mahajan
Erik Ingelsson
Allan Linneberg
Andrew R. Wood
Oddgeir L. Holmen
Nicola L. Beer
Mark I. McCarthy
Frank B. Hu
Peter Almgren
Heiner Boeing
Peter Donnelly
Carl Platou
Veikko Salomaa
Karl-Heinz Jöcke
Wen-Hong L. Kao
Lori L. Bonnycastle
Denis Rybin
Benjamin F. Voight
Peter Kraft
Inês Barroso
Claudia Langenberg
Teresa Ferreira
Peter Kovacs
Anne Raimondo
Christian Theil Have
Ulf de Faire
Torben Hansen
Han Chen
James B. Meigs
Timothy M. Frayling
Noël P. Burtt
Gerald Steinbach
Eric Boerwinkle
Michael Stumvoll
Stefan Gustafsson
Lars Lind
Andrew D. Morris
Alena Stančáková
Panagiotis Deloukas
Kari Stefansson
Augustine Kong
Hans A. Kestler
Andrew T. Hattersley
Beverley Balkau
Lorenzo Pasquali
Yingchang Lu
Nicola D. Kerrison
George B. Grant
Eeva Korpi-Hyövälti
Steven Wiltshire
Karl Gertow
Jorge Ferrer
Barbara Thorand
Inga Prokopenko
Matthias Blüher
Yvonne T. van der Schouw
Olga McLeod
Oluf Pedersen
Leena Peltonen
Anil Chalisey
Eleftheria Zeggini
Joseph Trakalo
Eric J.G. Sijbrands
Rainer Rauramaa
Guillaume Charpentier
Satu Männistö
Cordelia Langford
Lewin Eisele
Damiano Baldassarre
Lennart C. Karssen
Rona J. Strawbridge
Ghazala Mirza
Peter S. Chines
Roman Wennauer
Sara M. Willems
Erwin P. Bottinger
Timo Saaristo
Stéphane Cauchi
Ching-Ti Liu
Martijn van de Bunt
Valgerdur Steinthorsdottir
David Altshuler
Hyun Min Kang
Michael Boehnke
Jaakko Tuomilehto
Peter M. Nilsson
Kyle J. Gaulton
Jian'an Luan
Loic Yengo
David Couper
Reedik Mägi
Harald Grallert
Simone Wahl
Juha Saltevo
Phoenix Kwan
Cecilia M. Lindgren
Peter Lichtner
Richard N. Bergman
Andrew Crenshaw
João Fadista
Michael Roden
Annette Peters
Robert A. Scott
Unnur Thorsteinsdottir
James S. Pankow
Yeji Lee
Cornelia M. van Duijn
Samuli Ripatti
Francis S. Collins
Stéphane Lobbens
Niels Grarup
Ruth J. F. Loos
Julia Meyer
Marit E. Jørgensen
Christian Herder
Inger Njølstad
John R. B. Perry
Markus M. Nöthen
Man Li
Martina Müller-Nurasyid
Valeriya Lyssenko
Pierre Fontanillas
Michael D. Linderman
Leena Kinnunen
Jana K. Rundle
Elena Tremoli
Marilyn C. Cornelis
Tanya M. Teslovich
Todd Green
Raimund Erbel
Elisabeth M. van Leeuwen
Bengt Sennblad
Olle Melander
Sirkka Keinänen-Kiukaanniemi
Markku Laakso
Eero Lindholm
Alex S. F. Doney
Anke Tönjes
Maija Hassinen
Thomas W. Mühleisen
Gonçalo R. Abecasis
Nancy L. Pedersen
Thomas Sparsø
Johanna Kuusisto
Dorothée Thuillier
Qi Sun
Ian Dunham
Himanshu Chheda
Adam E. Locke
Philippe Froguel
Nicholas J. Wareham
Bruna Gigante
Jose C. Florez
Mozhgan Dorkhan
Omri Gottesman
Liming Liang
Anna Jonsson
Tiinamaija Tuomi
Leif Groop
Steve E. Humphries
Heikki A. Koistinen
Kristian Hveem
Astradur B. Hreidarsson
Jason Flannick
Torben Jørgensen
Clement Ma
Mattias Frånberg
Ewan Birney
Andrew P. Morris
Timo A. Lakka
Rob M. van Dam
Heather M. Stringham
Christian Gieger
Elodie Eury
Konstantin Strauch
Anna L. Gloyn
Rafn Benediktsson
Andres Metspalu
David J. Hunter
Karen L. Mohlke
Gudmar Thorleifsson
Josée Dupuis
Emmi Tikkanen
Christian Fuchsberger
Evelin Mihailov
Christopher J. Groves
Soren K. Thomsen
Tõnu Esko
Anne U. Jackson
Karin Leander
Douglas M. Ruderfer
Nikolay Oskolkov
Sekar Kathiresan
Robert Sladek
Lu Qi
Jasmina Kravic
Carmen Navarro
Epidemiology
Dermatology
Internal Medicine
ACS - Amsterdam Cardiovascular Sciences
Vascular Medicine
Cardiology
Wellcome Trust
Imperial College Healthcare NHS Trust- BRC Funding
Medical Research Council (MRC)
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Luan, Jian'an [0000-0003-3137-6337]
Perry, John [0000-0001-6483-3771]
Barroso, Ines [0000-0001-5800-4520]
Langenberg, Claudia [0000-0002-5017-7344]
Wareham, Nicholas [0000-0003-1422-2993]
Apollo - University of Cambridge Repository
Source :
Nature Genetics, 47, 1415. Nature Publishing Group, Nature Genetics, 47(12), 1415-+. Nature Publishing Group, Nature genetics, 47(12), 1415-+. Nature Publishing Group, Gaulton, K J, Ferreira, T, Lee, Y, Raimondo, A, Mägi, R, Reschen, M E, Mahajan, A, Locke, A E, Rayner, N W, Robertson, N, Scott, R A, Prokopenko, I, Scott, L J, Green, T, Sparso, T, Thuillier, D, Yengo, L, Grallert, H, Wahl, S, Frånberg, M, Strawbridge, R J, Kestler, H, Chheda, H, Eisele, L, Gustafsson, S, Steinthorsdottir, V, Thorleifsson, G, Qi, L, Karssen, L C, van Leeuwen, E M, Willems, S M, Li, M, Chen, H, Fuchsberger, C, Kwan, P, Ma, C, Linderman, M, Lu, Y, Thomsen, S K, Rundle, J K, Beer, N L, van de Bunt, M, Chalisey, A, Kang, H M, Voight, B F, Abecasis, G R, Almgren, P, Baldassarre, D, Jørgensen, M E, Hansen, T & DIAGRAM Consortium 2015, ' Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ', Nature Genetics, vol. 47, no. 12, pp. 1415-1425 . https://doi.org/10.1038/ng.3437, Nature Genetics, Gaulton, K J, Ferreira, T, Lee, Y, Raimondo, A, Mägi, R, Reschen, M E, Mahajan, A, Locke, A, William Rayner, N, Robertson, N, Scott, R A, Prokopenko, I, Scott, L J, Green, T, Sparso, T, Thuillier, D, Yengo, L, Grallert, H, Wahl, S, Frånberg, M, Strawbridge, R J, Kestler, H, Chheda, H, Eisele, L, Gustafsson, S, Steinthorsdottir, V, Thorleifsson, G, Qi, L, Karssen, L C, van Leeuwen, E M, Willems, S M, Li, M, Chen, H, Fuchsberger, C, Kwan, P, Ma, C, Linderman, M, Lu, Y, Thomsen, S K, Rundle, J K, Beer, N L, van de Bunt, M, Chalisey, A, Kang, H M, Voight, B F, Abecasis, G R, Almgren, P, Baldassarre, D, Balkau, B, Jørgensen, T & DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium 2015, ' Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ', Nature Genetics, vol. 47, no. 12, pp. 1415-1425 . https://doi.org/10.1038/ng.3437, Nature genetics, Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Publication Year :
2015

Abstract

To access publisher's full text version of this article click on the hyperlink at the bottom of the page We performed fine mapping of 39 established type 2 diabetes (T2D) loci in 27,206 cases and 57,574 controls of European ancestry. We identified 49 distinct association signals at these loci, including five mapping in or near KCNQ1. 'Credible sets' of the variants most likely to drive each distinct signal mapped predominantly to noncoding sequence, implying that association with T2D is mediated through gene regulation. Credible set variants were enriched for overlap with FOXA2 chromatin immunoprecipitation binding sites in human islet and liver cells, including at MTNR1B, where fine mapping implicated rs10830963 as driving T2D association. We confirmed that the T2D risk allele for this SNP increases FOXA2-bound enhancer activity in islet- and liver-derived cells. We observed allele-specific differences in NEUROD1 binding in islet-derived cells, consistent with evidence that the T2D risk allele increases islet MTNR1B expression. Our study demonstrates how integration of genetic and genomic information can define molecular mechanisms through which variants underlying association signals exert their effects on disease. cademy of Finland 77299 102318 10493 118065 123885 124243 129293 129680 136895 139635 211119 213506 251217 263836 Agence National de la Recherche Association de Langue Francaise pour l'Etude du Diabete et des Maladies Metaboliques Association Diabeete Risque Vasculaire Association Francaise des Diabetiques Association of Danish Pharmacies Augustinus Foundation Becket Foundation British Diabetes Association (BDA) Research British Heart Foundation Central Norway Health Authority Central Finland Hospital District Center for Inherited Disease Research (CIDR) City of Kuopio City of Leutkirch Copenhagen County Danish Centre for Evaluation and Health Technology Assessment Danish Council for Independent Research Danish Heart Foundation Danish Research Councils Deutsche Forschungsgemeinschaft ER 155/6-2 Diabetes Research Foundation Diabetes UK Doris Duke Charitable Foundation Erasmus Medical Center Erasmus University Estonian government SF0180142s08 European Commission ENGAGE HEALTH-F4-2007-201413 FP7-201413 FP7-245536 EXGENESIS LSHM-CT-2004-005272 FP6 LSHM_CT_2006_037197 LSHM-CT-2007-037273 C-Public Health 2004310 European Regional Development Fund Federal Ministry of Education and Research, Germany FKZ 01GI1128 FKZ 01EO1001 Federal Ministry of Health, Germany Finnish Diabetes Association Finnish Diabetes Research Foundation Finnish Foundation for Cardiovascular Research Finnish Medical Society Folkhalsan Research Foundation Foundation for Life and Health in Finland Foundation for Old Servants Fredrick och Ingrid Thuring Foundation French region of Nord-Pas-de-Calais (Contrat de Projets Etat-Region) German Center for Diabetes Research German Research Council GRK1041 German National Genome Research Network Groupe d'Etude des Maladies Metaboliques et Systemiques Health Care Centers in Vasa, Narpes and Korsholm, Finland Health Foundation Heinz Nixdorf Foundation Helmholtz Zentrum Munchen Helsinki University Central Hospital Research Foundation Hospital District of Southwest Finland Ib Henriksens Foundation IngaBritt and Arne Lundberg's Research Foundation 359 Karolinska Institutet Knut and Alice Wallenberg Foundation KAW 2009.0243 Kuopio University Hospital Lundbeck Foundation Magnus Bergvall Foundation Medical Faculty of University Duisburg-Essen Medical Research Council, UK G0000649 G0601261 Ministry for Health, Welfare and Sports, the Netherlands Ministry of Education and Culture, Finland 722 627 Ministry of Education, Culture and Science, the Netherlands Ministry of Health and Prevention, Denmark Ministry of Social Affairs and Health, Finland Ministry of Innovation, Science, Research and Technology of North Rhine-Westphalia, Germany Munich Center of Health Sciences Municipal Health Care Center and Hospital in Jakobstad, Finland municipality of Rotterdam, the Netherlands Narpes Health Care Foundation National Health Screening Service of Norway National Heart, Lung, and Blood Institute, USA HHSN268201100005C HHSN268201100006C HHSN268201100007C HHSN268201100008C HHSN268201100009C HHSN268201100010C HHSN268201100011C HHSN268201100012C N01HC25195 N02HL64278 R01HL087641 R01HL59367 R01HL086694 National Human Genome Research Institute, USA U01HG004402 N01HG65403 National Institute for Diabetes and Digestive and Kidney Diseases, USA R01DK078616 U01DK085526 K24DK080140 R01DK073490 National Institute for Health and Welfare, Finland National Institutes of Health, USA HHSN268200625226C UL1RR025005 R01DK062370 R01DK072193 1Z01HG000024 AG028555 AG08724 AG04563 AG10175 AG08861 U01HG004399 DK58845 CA055075 DK085545 DK098032 Netherlands Genomics Initiative Netherlands Organisation for Health Research and Development Netherlands Organisation of Scientific Research NOW Investments 175.010.2005.011 911-03-012 050-060-810 Nord-Trondelag County Council Nordic Center of Excellence in Disease Genetics Norwegian Institute of Public Health Norwegian Research Council Novo Nordisk Foundation Ollquist Foundation Oxford National Institute for Health Research (NIHR) Biomedical Research Centre Paavo Nurmi Foundation Paivikki and Sakari Sohlberg Foundation Perklen Foundation Pirkanmaa Hospital District, Finland Programme Hospitalier de Recherche Clinique Programme National de Recherche sur la Diabete Research Institute for Diseases in the Elderly 014-93-015 Robert Dawson Evans Endowment, Department of Medicine, Boston University School of Medicine and Boston Medical Center Royal Swedish Academy of Sciences Sarstedt, Germany Signe and Ane Gyllenberg Foundation Sigrid Juselius Foundation Slottery Machine Association, Finland Social Insurance Institution of Finland South OstroBothnia Hospital District state of Baden-Wurttemberg, Germany Stockholm County Council 560183 Swedish Cultural Foundation, Finland Swedish Diabetes Foundation Swedish e-science Research Center Swedish Foundation for Strategic Research Swedish Heart-Lung Foundation Swedish Research Council SFO EXODIAB 2009-1039 521-2010-3490 521-2007-4037 521-2008-2974 ANDIS 825-2010-5983 LUDC 349-2008-6589 8691 Swedish Society of Medicine Tore Nilsson Foundation Torsten and Ragnar Soderbergs Stiftelser MT33/09 University Hospital Essen University of Tromso University College London NIHR Biomedical Research Centre UK NIHR Cambridge Biomedical Research Centre Uppsala University Uppsala University Hospital Vaasa Hospital District Velux Foundation Wellcome Trust GR072960 076113 083948 090367 090532 083270 086596 098017 095101 098051 098381

Details

Language :
English
ISSN :
10614036
Database :
OpenAIRE
Journal :
Nature Genetics, 47, 1415. Nature Publishing Group, Nature Genetics, 47(12), 1415-+. Nature Publishing Group, Nature genetics, 47(12), 1415-+. Nature Publishing Group, Gaulton, K J, Ferreira, T, Lee, Y, Raimondo, A, Mägi, R, Reschen, M E, Mahajan, A, Locke, A E, Rayner, N W, Robertson, N, Scott, R A, Prokopenko, I, Scott, L J, Green, T, Sparso, T, Thuillier, D, Yengo, L, Grallert, H, Wahl, S, Frånberg, M, Strawbridge, R J, Kestler, H, Chheda, H, Eisele, L, Gustafsson, S, Steinthorsdottir, V, Thorleifsson, G, Qi, L, Karssen, L C, van Leeuwen, E M, Willems, S M, Li, M, Chen, H, Fuchsberger, C, Kwan, P, Ma, C, Linderman, M, Lu, Y, Thomsen, S K, Rundle, J K, Beer, N L, van de Bunt, M, Chalisey, A, Kang, H M, Voight, B F, Abecasis, G R, Almgren, P, Baldassarre, D, Jørgensen, M E, Hansen, T & DIAGRAM Consortium 2015, ' Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ', Nature Genetics, vol. 47, no. 12, pp. 1415-1425 . https://doi.org/10.1038/ng.3437, Nature Genetics, Gaulton, K J, Ferreira, T, Lee, Y, Raimondo, A, Mägi, R, Reschen, M E, Mahajan, A, Locke, A, William Rayner, N, Robertson, N, Scott, R A, Prokopenko, I, Scott, L J, Green, T, Sparso, T, Thuillier, D, Yengo, L, Grallert, H, Wahl, S, Frånberg, M, Strawbridge, R J, Kestler, H, Chheda, H, Eisele, L, Gustafsson, S, Steinthorsdottir, V, Thorleifsson, G, Qi, L, Karssen, L C, van Leeuwen, E M, Willems, S M, Li, M, Chen, H, Fuchsberger, C, Kwan, P, Ma, C, Linderman, M, Lu, Y, Thomsen, S K, Rundle, J K, Beer, N L, van de Bunt, M, Chalisey, A, Kang, H M, Voight, B F, Abecasis, G R, Almgren, P, Baldassarre, D, Balkau, B, Jørgensen, T & DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium 2015, ' Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci ', Nature Genetics, vol. 47, no. 12, pp. 1415-1425 . https://doi.org/10.1038/ng.3437, Nature genetics, Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid
Accession number :
edsair.doi.dedup.....0d0b5ee13e5230169a934120dd03c1e8