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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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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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. |
format | Online Article Text |
id | pubmed-6248311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
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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