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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation

We apply integrative approaches to expression quantitative loci (eQTLs) from 44 tissues from the GTEx Project and genome-wide association study (GWAS) data. About 60% of known trait-associated loci are in linkage disequilibrium with a cis-eQTL, over half of which were not found in previous large-sca...

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Autores principales: Gamazon, Eric R., Segrè, Ayellet V., van de Bunt, Martijn, Wen, Xiaoquan, Xi, Hualin S., Hormozdiari, Farhad, Ongen, Halit, Konkashbaev, Anuar, Derks, Eske M., Aguet, François, Quan, Jie, Nicolae, Dan L., Eskin, Eleazar, Kellis, Manolis, Getz, Gad, McCarthy, Mark I., Dermitzakis, Emmanouil T., Cox, Nancy J., Ardlie, Kristin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248311/
https://www.ncbi.nlm.nih.gov/pubmed/29955180
http://dx.doi.org/10.1038/s41588-018-0154-4
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author Gamazon, Eric R.
Segrè, Ayellet V.
van de Bunt, Martijn
Wen, Xiaoquan
Xi, Hualin S.
Hormozdiari, Farhad
Ongen, Halit
Konkashbaev, Anuar
Derks, Eske M.
Aguet, François
Quan, Jie
Nicolae, Dan L.
Eskin, Eleazar
Kellis, Manolis
Getz, Gad
McCarthy, Mark I.
Dermitzakis, Emmanouil T.
Cox, Nancy J.
Ardlie, Kristin G.
author_facet Gamazon, Eric R.
Segrè, Ayellet V.
van de Bunt, Martijn
Wen, Xiaoquan
Xi, Hualin S.
Hormozdiari, Farhad
Ongen, Halit
Konkashbaev, Anuar
Derks, Eske M.
Aguet, François
Quan, Jie
Nicolae, Dan L.
Eskin, Eleazar
Kellis, Manolis
Getz, Gad
McCarthy, Mark I.
Dermitzakis, Emmanouil T.
Cox, Nancy J.
Ardlie, Kristin G.
author_sort Gamazon, Eric R.
collection PubMed
description We apply integrative approaches to expression quantitative loci (eQTLs) from 44 tissues from the GTEx Project and genome-wide association study (GWAS) data. About 60% of known trait-associated loci are in linkage disequilibrium with a cis-eQTL, over half of which were not found in previous large-scale whole blood studies. Applying polygenic analyses to metabolic, cardiovascular, anthropometric, autoimmune, and neurodegenerative traits, we find that eQTLs are significantly enriched for trait associations in relevant pathogenic tissues and explain a substantial proportion of the heritability (40-80%). For most traits, tissue-shared eQTLs underlie a greater proportion of trait associations, though tissue-specific eQTLs have a greater contribution to some traits, such as blood pressure. By integrating information from biological pathways with eQTL target genes and applying a gene-based approach, we validate previously implicated causal genes and pathways, and propose new variant- and gene-associations for several complex traits, which we replicate in the UK BioBank and BioVU.
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spelling pubmed-62483112018-12-28 Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation Gamazon, Eric R. Segrè, Ayellet V. van de Bunt, Martijn Wen, Xiaoquan Xi, Hualin S. Hormozdiari, Farhad Ongen, Halit Konkashbaev, Anuar Derks, Eske M. Aguet, François Quan, Jie Nicolae, Dan L. Eskin, Eleazar Kellis, Manolis Getz, Gad McCarthy, Mark I. Dermitzakis, Emmanouil T. Cox, Nancy J. Ardlie, Kristin G. Nat Genet Article We apply integrative approaches to expression quantitative loci (eQTLs) from 44 tissues from the GTEx Project and genome-wide association study (GWAS) data. About 60% of known trait-associated loci are in linkage disequilibrium with a cis-eQTL, over half of which were not found in previous large-scale whole blood studies. Applying polygenic analyses to metabolic, cardiovascular, anthropometric, autoimmune, and neurodegenerative traits, we find that eQTLs are significantly enriched for trait associations in relevant pathogenic tissues and explain a substantial proportion of the heritability (40-80%). For most traits, tissue-shared eQTLs underlie a greater proportion of trait associations, though tissue-specific eQTLs have a greater contribution to some traits, such as blood pressure. By integrating information from biological pathways with eQTL target genes and applying a gene-based approach, we validate previously implicated causal genes and pathways, and propose new variant- and gene-associations for several complex traits, which we replicate in the UK BioBank and BioVU. 2018-06-28 2018-07 /pmc/articles/PMC6248311/ /pubmed/29955180 http://dx.doi.org/10.1038/s41588-018-0154-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Gamazon, Eric R.
Segrè, Ayellet V.
van de Bunt, Martijn
Wen, Xiaoquan
Xi, Hualin S.
Hormozdiari, Farhad
Ongen, Halit
Konkashbaev, Anuar
Derks, Eske M.
Aguet, François
Quan, Jie
Nicolae, Dan L.
Eskin, Eleazar
Kellis, Manolis
Getz, Gad
McCarthy, Mark I.
Dermitzakis, Emmanouil T.
Cox, Nancy J.
Ardlie, Kristin G.
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title_full Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title_fullStr Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title_full_unstemmed Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title_short Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
title_sort using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248311/
https://www.ncbi.nlm.nih.gov/pubmed/29955180
http://dx.doi.org/10.1038/s41588-018-0154-4
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