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Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma

BACKGROUND: Many studies have attempted to identify gene-gene interactions affecting asthma susceptibility. However, these studies have typically used candidate gene approaches in limiting the genetic search space, and there have been few searches for gene-gene interactions on a genome-wide scale. W...

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Autores principales: Murk, William, DeWan, Andrew T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936310/
https://www.ncbi.nlm.nih.gov/pubmed/27387956
http://dx.doi.org/10.1186/s12863-016-0376-3
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author Murk, William
DeWan, Andrew T.
author_facet Murk, William
DeWan, Andrew T.
author_sort Murk, William
collection PubMed
description BACKGROUND: Many studies have attempted to identify gene-gene interactions affecting asthma susceptibility. However, these studies have typically used candidate gene approaches in limiting the genetic search space, and there have been few searches for gene-gene interactions on a genome-wide scale. We aimed to conduct a genome-wide gene-gene interaction study for asthma, using data from the GABRIEL Consortium. RESULTS: A two-stage study design was used, including a screening analysis (N = 1625 subjects) and a follow-up analysis (N = 5264 subjects). In the screening analysis, all pairwise interactions among 301,547 SNPs were evaluated, encompassing a total of 4.55 × 10(10) interactions. Those with a screening interaction p-value < 10(−5) were evaluated in the follow-up analysis. No interaction selected from the screening analysis met strict statistical significance in the follow-up (p-value < 1.45 × 10(−7)). However, the top-ranked interaction (rs910652 [20p13] × rs11684871 [2q14]) in the follow-up (p-value = 1.58 × 10(−6)) was significant in one component of a replication analysis. This interaction was notable in that rs910652 is located within 78 kilobases of ADAM33, which is one of the most well studied asthma susceptibility genes. In addition, rs11684871 is located in or near GLI2, which may have biologically relevant roles in asthma. CONCLUSIONS: Using a genome-wide approach, we identified and found suggestive evidence of replication for a gene-gene interaction in asthma involving loci that are potentially highly relevant in asthma pathogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-016-0376-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-49363102016-07-08 Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma Murk, William DeWan, Andrew T. BMC Genet Research Article BACKGROUND: Many studies have attempted to identify gene-gene interactions affecting asthma susceptibility. However, these studies have typically used candidate gene approaches in limiting the genetic search space, and there have been few searches for gene-gene interactions on a genome-wide scale. We aimed to conduct a genome-wide gene-gene interaction study for asthma, using data from the GABRIEL Consortium. RESULTS: A two-stage study design was used, including a screening analysis (N = 1625 subjects) and a follow-up analysis (N = 5264 subjects). In the screening analysis, all pairwise interactions among 301,547 SNPs were evaluated, encompassing a total of 4.55 × 10(10) interactions. Those with a screening interaction p-value < 10(−5) were evaluated in the follow-up analysis. No interaction selected from the screening analysis met strict statistical significance in the follow-up (p-value < 1.45 × 10(−7)). However, the top-ranked interaction (rs910652 [20p13] × rs11684871 [2q14]) in the follow-up (p-value = 1.58 × 10(−6)) was significant in one component of a replication analysis. This interaction was notable in that rs910652 is located within 78 kilobases of ADAM33, which is one of the most well studied asthma susceptibility genes. In addition, rs11684871 is located in or near GLI2, which may have biologically relevant roles in asthma. CONCLUSIONS: Using a genome-wide approach, we identified and found suggestive evidence of replication for a gene-gene interaction in asthma involving loci that are potentially highly relevant in asthma pathogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-016-0376-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-07 /pmc/articles/PMC4936310/ /pubmed/27387956 http://dx.doi.org/10.1186/s12863-016-0376-3 Text en © The Author(s). 2016 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 Research Article
Murk, William
DeWan, Andrew T.
Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title_full Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title_fullStr Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title_full_unstemmed Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title_short Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
title_sort genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936310/
https://www.ncbi.nlm.nih.gov/pubmed/27387956
http://dx.doi.org/10.1186/s12863-016-0376-3
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