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Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies

Genetic risk for complex traits is strongly enriched in non-coding genomic regions involved in gene regulation, especially enhancers. However, we lack adequate tools to connect the characteristics of these disruptions to genetic risk. Here, we propose RWAS (Regulome Wide Association Study), a new ap...

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Autores principales: Casella, Alex M., Colantuoni, Carlo, Ament, Seth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484640/
https://www.ncbi.nlm.nih.gov/pubmed/36070311
http://dx.doi.org/10.1371/journal.pcbi.1010430
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author Casella, Alex M.
Colantuoni, Carlo
Ament, Seth A.
author_facet Casella, Alex M.
Colantuoni, Carlo
Ament, Seth A.
author_sort Casella, Alex M.
collection PubMed
description Genetic risk for complex traits is strongly enriched in non-coding genomic regions involved in gene regulation, especially enhancers. However, we lack adequate tools to connect the characteristics of these disruptions to genetic risk. Here, we propose RWAS (Regulome Wide Association Study), a new application of the MAGMA software package to identify the characteristics of enhancers that contribute to genetic risk for disease. RWAS involves three steps: (i) assign genotyped SNPs to cell type- or tissue-specific regulatory features (e.g., enhancers); (ii) test associations of each regulatory feature with a trait of interest for which genome-wide association study (GWAS) summary statistics are available; (iii) perform enhancer-set enrichment analyses to identify quantitative or categorical features of regulatory elements that are associated with the trait. These steps are implemented as a novel application of MAGMA, a tool originally developed for gene-based GWAS analyses. Applying RWAS to interrogate genetic risk for schizophrenia, we discovered a class of risk-associated AT-rich enhancers that are active in the developing brain and harbor binding sites for multiple transcription factors with neurodevelopmental functions. RWAS utilizes open-source software, and we provide a comprehensive collection of annotations for tissue-specific enhancer locations and features, including their evolutionary conservation, AT content, and co-localization with binding sites for hundreds of TFs. RWAS will enable researchers to characterize properties of regulatory elements associated with any trait of interest for which GWAS summary statistics are available.
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spelling pubmed-94846402022-09-20 Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies Casella, Alex M. Colantuoni, Carlo Ament, Seth A. PLoS Comput Biol Research Article Genetic risk for complex traits is strongly enriched in non-coding genomic regions involved in gene regulation, especially enhancers. However, we lack adequate tools to connect the characteristics of these disruptions to genetic risk. Here, we propose RWAS (Regulome Wide Association Study), a new application of the MAGMA software package to identify the characteristics of enhancers that contribute to genetic risk for disease. RWAS involves three steps: (i) assign genotyped SNPs to cell type- or tissue-specific regulatory features (e.g., enhancers); (ii) test associations of each regulatory feature with a trait of interest for which genome-wide association study (GWAS) summary statistics are available; (iii) perform enhancer-set enrichment analyses to identify quantitative or categorical features of regulatory elements that are associated with the trait. These steps are implemented as a novel application of MAGMA, a tool originally developed for gene-based GWAS analyses. Applying RWAS to interrogate genetic risk for schizophrenia, we discovered a class of risk-associated AT-rich enhancers that are active in the developing brain and harbor binding sites for multiple transcription factors with neurodevelopmental functions. RWAS utilizes open-source software, and we provide a comprehensive collection of annotations for tissue-specific enhancer locations and features, including their evolutionary conservation, AT content, and co-localization with binding sites for hundreds of TFs. RWAS will enable researchers to characterize properties of regulatory elements associated with any trait of interest for which GWAS summary statistics are available. Public Library of Science 2022-09-07 /pmc/articles/PMC9484640/ /pubmed/36070311 http://dx.doi.org/10.1371/journal.pcbi.1010430 Text en © 2022 Casella et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Casella, Alex M.
Colantuoni, Carlo
Ament, Seth A.
Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title_full Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title_fullStr Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title_full_unstemmed Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title_short Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
title_sort identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484640/
https://www.ncbi.nlm.nih.gov/pubmed/36070311
http://dx.doi.org/10.1371/journal.pcbi.1010430
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