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From association to mechanism in complex disease genetics: the role of the 3D genome
Genome-wide association studies (GWAS) and fine mapping studies in autoimmune diseases have identified thousands of genetic variants, the majority of which are located in non-protein-coding enhancer regions. Enhancers function within the context of the three-dimensional (3D) genome to form long-rang...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162955/ https://www.ncbi.nlm.nih.gov/pubmed/30268153 http://dx.doi.org/10.1186/s13075-018-1721-x |
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author | Fu, Yao Tessneer, Kandice L Li, Chuang Gaffney, Patrick M |
author_facet | Fu, Yao Tessneer, Kandice L Li, Chuang Gaffney, Patrick M |
author_sort | Fu, Yao |
collection | PubMed |
description | Genome-wide association studies (GWAS) and fine mapping studies in autoimmune diseases have identified thousands of genetic variants, the majority of which are located in non-protein-coding enhancer regions. Enhancers function within the context of the three-dimensional (3D) genome to form long-range DNA looping events with target gene promoters that spatially and temporally regulate gene expression. Investigating the functional significance of GWAS variants in the context of the 3D genome is essential for mechanistic understanding of these variants and how they influence disease pathology by altering DNA looping between enhancers and the target gene promoters they regulate. In this review, we discuss the functional complexity of the 3D genome and the technological approaches used to characterize DNA looping events. We then highlight examples from the literature that illustrate how functional mapping of the 3D genome can assist in defining mechanisms that influence pathogenic gene expression. We conclude by highlighting future advances necessary to fully integrate 3D genome analyses into the functional workup of GWAS variants in the continuing effort to improve the health of patients with autoimmune diseases. |
format | Online Article Text |
id | pubmed-6162955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61629552018-10-04 From association to mechanism in complex disease genetics: the role of the 3D genome Fu, Yao Tessneer, Kandice L Li, Chuang Gaffney, Patrick M Arthritis Res Ther Review Genome-wide association studies (GWAS) and fine mapping studies in autoimmune diseases have identified thousands of genetic variants, the majority of which are located in non-protein-coding enhancer regions. Enhancers function within the context of the three-dimensional (3D) genome to form long-range DNA looping events with target gene promoters that spatially and temporally regulate gene expression. Investigating the functional significance of GWAS variants in the context of the 3D genome is essential for mechanistic understanding of these variants and how they influence disease pathology by altering DNA looping between enhancers and the target gene promoters they regulate. In this review, we discuss the functional complexity of the 3D genome and the technological approaches used to characterize DNA looping events. We then highlight examples from the literature that illustrate how functional mapping of the 3D genome can assist in defining mechanisms that influence pathogenic gene expression. We conclude by highlighting future advances necessary to fully integrate 3D genome analyses into the functional workup of GWAS variants in the continuing effort to improve the health of patients with autoimmune diseases. BioMed Central 2018-09-29 2018 /pmc/articles/PMC6162955/ /pubmed/30268153 http://dx.doi.org/10.1186/s13075-018-1721-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Fu, Yao Tessneer, Kandice L Li, Chuang Gaffney, Patrick M From association to mechanism in complex disease genetics: the role of the 3D genome |
title | From association to mechanism in complex disease genetics: the role of the 3D genome |
title_full | From association to mechanism in complex disease genetics: the role of the 3D genome |
title_fullStr | From association to mechanism in complex disease genetics: the role of the 3D genome |
title_full_unstemmed | From association to mechanism in complex disease genetics: the role of the 3D genome |
title_short | From association to mechanism in complex disease genetics: the role of the 3D genome |
title_sort | from association to mechanism in complex disease genetics: the role of the 3d genome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162955/ https://www.ncbi.nlm.nih.gov/pubmed/30268153 http://dx.doi.org/10.1186/s13075-018-1721-x |
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