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Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits

Regulation of gene expression is an important mechanism through which genetic variation can affect complex traits. A substantial portion of gene expression variation can be explained by both local (cis) and distal (trans) genetic variation. Much progress has been made in uncovering cis‐acting expres...

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Autores principales: Wheeler, Heather E., Ploch, Sally, Barbeira, Alvaro N., Bonazzola, Rodrigo, Andaleon, Angela, Fotuhi Siahpirani, Alireza, Saha, Ashis, Battle, Alexis, Roy, Sushmita, Im, Hae Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687523/
https://www.ncbi.nlm.nih.gov/pubmed/30950127
http://dx.doi.org/10.1002/gepi.22205
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author Wheeler, Heather E.
Ploch, Sally
Barbeira, Alvaro N.
Bonazzola, Rodrigo
Andaleon, Angela
Fotuhi Siahpirani, Alireza
Saha, Ashis
Battle, Alexis
Roy, Sushmita
Im, Hae Kyung
author_facet Wheeler, Heather E.
Ploch, Sally
Barbeira, Alvaro N.
Bonazzola, Rodrigo
Andaleon, Angela
Fotuhi Siahpirani, Alireza
Saha, Ashis
Battle, Alexis
Roy, Sushmita
Im, Hae Kyung
author_sort Wheeler, Heather E.
collection PubMed
description Regulation of gene expression is an important mechanism through which genetic variation can affect complex traits. A substantial portion of gene expression variation can be explained by both local (cis) and distal (trans) genetic variation. Much progress has been made in uncovering cis‐acting expression quantitative trait loci (cis‐eQTL), but trans‐eQTL have been more difficult to identify and replicate. Here we take advantage of our ability to predict the cis component of gene expression coupled with gene mapping methods such as PrediXcan to identify high confidence candidate trans‐acting genes and their targets. That is, we correlate the cis component of gene expression with observed expression of genes in different chromosomes. Leveraging the shared cis‐acting regulation across tissues, we combine the evidence of association across all available Genotype‐Tissue Expression Project tissues and find 2,356 trans‐acting/target gene pairs with high mappability scores. Reassuringly, trans‐acting genes are enriched in transcription and nucleic acid binding pathways and target genes are enriched in known transcription factor binding sites. Interestingly, trans‐acting genes are more significantly associated with selected complex traits and diseases than target or background genes, consistent with percolating trans effects. Our scripts and summary statistics are publicly available for future studies of trans‐acting gene regulation.
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spelling pubmed-66875232019-10-01 Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits Wheeler, Heather E. Ploch, Sally Barbeira, Alvaro N. Bonazzola, Rodrigo Andaleon, Angela Fotuhi Siahpirani, Alireza Saha, Ashis Battle, Alexis Roy, Sushmita Im, Hae Kyung Genet Epidemiol Research Articles Regulation of gene expression is an important mechanism through which genetic variation can affect complex traits. A substantial portion of gene expression variation can be explained by both local (cis) and distal (trans) genetic variation. Much progress has been made in uncovering cis‐acting expression quantitative trait loci (cis‐eQTL), but trans‐eQTL have been more difficult to identify and replicate. Here we take advantage of our ability to predict the cis component of gene expression coupled with gene mapping methods such as PrediXcan to identify high confidence candidate trans‐acting genes and their targets. That is, we correlate the cis component of gene expression with observed expression of genes in different chromosomes. Leveraging the shared cis‐acting regulation across tissues, we combine the evidence of association across all available Genotype‐Tissue Expression Project tissues and find 2,356 trans‐acting/target gene pairs with high mappability scores. Reassuringly, trans‐acting genes are enriched in transcription and nucleic acid binding pathways and target genes are enriched in known transcription factor binding sites. Interestingly, trans‐acting genes are more significantly associated with selected complex traits and diseases than target or background genes, consistent with percolating trans effects. Our scripts and summary statistics are publicly available for future studies of trans‐acting gene regulation. John Wiley and Sons Inc. 2019-04-04 2019-09 /pmc/articles/PMC6687523/ /pubmed/30950127 http://dx.doi.org/10.1002/gepi.22205 Text en © 2019 The Authors. Genetic Epidemiology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Wheeler, Heather E.
Ploch, Sally
Barbeira, Alvaro N.
Bonazzola, Rodrigo
Andaleon, Angela
Fotuhi Siahpirani, Alireza
Saha, Ashis
Battle, Alexis
Roy, Sushmita
Im, Hae Kyung
Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title_full Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title_fullStr Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title_full_unstemmed Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title_short Imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
title_sort imputed gene associations identify replicable trans‐acting genes enriched in transcription pathways and complex traits
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687523/
https://www.ncbi.nlm.nih.gov/pubmed/30950127
http://dx.doi.org/10.1002/gepi.22205
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