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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits.
Brown, Andrew A; Fernandez-Tajes, Juan J; Hong, Mun-Gwan; Brorsson, Caroline A; Koivula, Robert W; Davtian, David; Dupuis, Théo; Sartori, Ambra; Michalettou, Theodora-Dafni; Forgie, Ian M; Adam, Jonathan; Allin, Kristine H; Caiazzo, Robert; Cederberg, Henna; De Masi, Federico; Elders, Petra J M; Giordano, Giuseppe N; Haid, Mark; Hansen, Torben; Hansen, Tue H; Hattersley, Andrew T; Heggie, Alison J; Howald, Cédric; Jones, Angus G; Kokkola, Tarja; Laakso, Markku; Mahajan, Anubha; Mari, Andrea; McDonald, Timothy J; McEvoy, Donna; Mourby, Miranda; Musholt, Petra B; Nilsson, Birgitte; Pattou, Francois; Penet, Deborah; Raverdy, Violeta; Ridderstråle, Martin; Romano, Luciana; Rutters, Femke; Sharma, Sapna; Teare, Harriet; 't Hart, Leen; Tsirigos, Konstantinos D; Vangipurapu, Jagadish; Vestergaard, Henrik; Brunak, Søren; Franks, Paul W; Frost, Gary; Grallert, Harald; Jablonka, Bernd.
Afiliação
  • Brown AA; Population Health and Genomics, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, United Kingdom.
  • Fernandez-Tajes JJ; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, United Kingdom.
  • Hong MG; Science for Life Laboratory, School of Biotechnology, KTH - Royal Institute of Technology, Solna, SE-171 21, Sweden.
  • Brorsson CA; Department of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
  • Koivula RW; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, DK-2100, Denmark.
  • Davtian D; Oxford Centre for Diabetes Endocrinology and Metabolism, University of Oxford, Oxford, OX3 7LJ, United Kingdom.
  • Dupuis T; Population Health and Genomics, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, United Kingdom.
  • Sartori A; Population Health and Genomics, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, United Kingdom.
  • Michalettou TD; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, 1211, Switzerland.
  • Forgie IM; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, 1211, Switzerland.
  • Adam J; Swiss Institute of Bioinformatics, Geneva, 1211, Switzerland.
  • Allin KH; Biosciences Institute, Faculty of Medical Sciences, University of Newcastle, Newcastle upon Tyne, NE1 4EP, United Kingdom.
  • Caiazzo R; Population Health and Genomics, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, United Kingdom.
  • Cederberg H; German Center for Diabetes Research (DZD), Neuherberg, 85764, Germany.
  • De Masi F; Research Unit of Molecular Epidemiology, Institute of Epidemiology, German Research Center for Environmental Health, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
  • Elders PJM; The Novo Nordisk Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, DK-2100, Denmark.
  • Giordano GN; University of Lille, Inserm, Lille Pasteur Institute, Lille, France.
  • Haid M; Internal Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Hansen T; Department of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
  • Hansen TH; Department of General Practice, Amsterdam UMC- location Vumc, Amsterdam Public Health research institute, Amsterdam, The Netherlands.
  • Hattersley AT; Department of Clinical Science, Genetic and Molecular Epidemiology, Lund University Diabetes Centre, Malmö, Sweden.
  • Heggie AJ; Metabolomics and Proteomics Core, German Research Center for Environmental Health, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
  • Howald C; The Novo Nordisk Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, DK-2100, Denmark.
  • Jones AG; The Novo Nordisk Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, DK-2100, Denmark.
  • Kokkola T; Department of Clinical and Biomedical Sciences, University of Exeter College of Medicine & Health, Exeter, EX25DW, United Kingdom.
  • Laakso M; Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Mahajan A; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, 1211, Switzerland.
  • Mari A; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, 1211, Switzerland.
  • McDonald TJ; Swiss Institute of Bioinformatics, Geneva, 1211, Switzerland.
  • McEvoy D; Department of Clinical and Biomedical Sciences, University of Exeter College of Medicine & Health, Exeter, EX25DW, United Kingdom.
  • Mourby M; Internal Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Musholt PB; Internal Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
  • Nilsson B; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, United Kingdom.
  • Pattou F; Institute of Neuroscience, National Research Council, Padova, 35127, Italy.
  • Penet D; Blood Sciences, Royal Devon and Exeter NHS Foundation Trust, Exeter, EX2 5DW, United Kingdom.
  • Raverdy V; Diabetes Research Network, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Ridderstråle M; Nuffield Department of Population Health, Centre for Health, Law and Emerging Technologies (HeLEX), University of Oxford, Oxford, OX2 7DD, United Kingdom.
  • Romano L; Global Development, Sanofi-Aventis Deutschland GmbH, Hoechst Industrial Park, Frankfurt am Main, 65926, Germany.
  • Rutters F; Department of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
  • Sharma S; University of Lille, Inserm, Lille Pasteur Institute, Lille, France.
  • Teare H; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, 1211, Switzerland.
  • 't Hart L; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, 1211, Switzerland.
  • Tsirigos KD; Swiss Institute of Bioinformatics, Geneva, 1211, Switzerland.
  • Vangipurapu J; University of Lille, Inserm, Lille Pasteur Institute, Lille, France.
  • Vestergaard H; Department of Clinical Science, Lund University, Malmö, Sweden.
  • Brunak S; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, 1211, Switzerland.
  • Franks PW; Institute for Genetics and Genomics in Geneva (iGE3), University of Geneva, Geneva, 1211, Switzerland.
  • Frost G; Swiss Institute of Bioinformatics, Geneva, 1211, Switzerland.
  • Grallert H; Epidemiology and Data Science, VUMC, Amsterdam, The Netherlands.
  • Jablonka B; Research Unit of Molecular Epidemiology, Institute of Epidemiology, German Research Center for Environmental Health, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
Nat Commun ; 14(1): 5062, 2023 08 21.
Article em En | MEDLINE | ID: mdl-37604891
ABSTRACT
We evaluate the shared genetic regulation of mRNA molecules, proteins and metabolites derived from whole blood from 3029 human donors. We find abundant allelic heterogeneity, where multiple variants regulate a particular molecular phenotype, and pleiotropy, where a single variant associates with multiple molecular phenotypes over multiple genomic regions. The highest proportion of share genetic regulation is detected between gene expression and proteins (66.6%), with a further median shared genetic associations across 49 different tissues of 78.3% and 62.4% between plasma proteins and gene expression. We represent the genetic and molecular associations in networks including 2828 known GWAS variants, showing that GWAS variants are more often connected to gene expression in trans than other molecular phenotypes in the network. Our work provides a roadmap to understanding molecular networks and deriving the underlying mechanism of action of GWAS variants using different molecular phenotypes in an accessible tissue.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Herança Multifatorial / Genômica Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Herança Multifatorial / Genômica Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido