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Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease
BACKGROUND: Reduced lung function in patients with chronic obstructive pulmonary disease (COPD) is likely due to both environmental and genetic factors. We report here a targeted high-throughput DNA sequencing approach to identify new and previously known genetic variants in a set of candidate genes...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106844/ https://www.ncbi.nlm.nih.gov/pubmed/27835950 http://dx.doi.org/10.1186/s12890-016-0309-y |
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author | Matsson, Hans Söderhäll, Cilla Einarsdottir, Elisabet Lamontagne, Maxime Gudmundsson, Sanna Backman, Helena Lindberg, Anne Rönmark, Eva Kere, Juha Sin, Don Postma, Dirkje S. Bossé, Yohan Lundbäck, Bo Klar, Joakim |
author_facet | Matsson, Hans Söderhäll, Cilla Einarsdottir, Elisabet Lamontagne, Maxime Gudmundsson, Sanna Backman, Helena Lindberg, Anne Rönmark, Eva Kere, Juha Sin, Don Postma, Dirkje S. Bossé, Yohan Lundbäck, Bo Klar, Joakim |
author_sort | Matsson, Hans |
collection | PubMed |
description | BACKGROUND: Reduced lung function in patients with chronic obstructive pulmonary disease (COPD) is likely due to both environmental and genetic factors. We report here a targeted high-throughput DNA sequencing approach to identify new and previously known genetic variants in a set of candidate genes for COPD. METHODS: Exons in 22 genes implicated in lung development as well as 61 genes and 10 genomic regions previously associated with COPD were sequenced using individual DNA samples from 68 cases with moderate or severe COPD and 66 controls matched for age, gender and smoking. Cases and controls were selected from the Obstructive Lung Disease in Northern Sweden (OLIN) studies. RESULTS: In total, 37 genetic variants showed association with COPD (p < 0.05, uncorrected). Several variants previously discovered to be associated with COPD from genetic genome-wide analysis studies were replicated using our sample. Two high-risk variants were followed-up for functional characterization in a large eQTL mapping study of 1,111 human lung specimens. The C allele of a synonymous variant, rs8040868, predicting a p.(S45=) in the gene for cholinergic receptor nicotinic alpha 3 (CHRNA3) was associated with COPD (p = 8.8 x 10(−3)). This association remained (p = 0.003 and OR = 1.4, 95 % CI 1.1-1.7) when analysing all available cases and controls in OLIN (n = 1,534). The rs8040868 variant is in linkage disequilibrium with rs16969968 previously associated with COPD and altered expression of the CHRNA5 gene. A follow-up analysis for detection of expression quantitative trait loci revealed that rs8040868-C was found to be significantly associated with a decreased expression of the nearby gene cholinergic receptor, nicotinic, alpha 5 (CHRNA5) in lung tissue. CONCLUSION: Our data replicate previous result suggesting CHRNA5 as a candidate gene for COPD and rs8040868 as a risk variant for the development of COPD in the Swedish population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0309-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5106844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51068442016-11-28 Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease Matsson, Hans Söderhäll, Cilla Einarsdottir, Elisabet Lamontagne, Maxime Gudmundsson, Sanna Backman, Helena Lindberg, Anne Rönmark, Eva Kere, Juha Sin, Don Postma, Dirkje S. Bossé, Yohan Lundbäck, Bo Klar, Joakim BMC Pulm Med Research Article BACKGROUND: Reduced lung function in patients with chronic obstructive pulmonary disease (COPD) is likely due to both environmental and genetic factors. We report here a targeted high-throughput DNA sequencing approach to identify new and previously known genetic variants in a set of candidate genes for COPD. METHODS: Exons in 22 genes implicated in lung development as well as 61 genes and 10 genomic regions previously associated with COPD were sequenced using individual DNA samples from 68 cases with moderate or severe COPD and 66 controls matched for age, gender and smoking. Cases and controls were selected from the Obstructive Lung Disease in Northern Sweden (OLIN) studies. RESULTS: In total, 37 genetic variants showed association with COPD (p < 0.05, uncorrected). Several variants previously discovered to be associated with COPD from genetic genome-wide analysis studies were replicated using our sample. Two high-risk variants were followed-up for functional characterization in a large eQTL mapping study of 1,111 human lung specimens. The C allele of a synonymous variant, rs8040868, predicting a p.(S45=) in the gene for cholinergic receptor nicotinic alpha 3 (CHRNA3) was associated with COPD (p = 8.8 x 10(−3)). This association remained (p = 0.003 and OR = 1.4, 95 % CI 1.1-1.7) when analysing all available cases and controls in OLIN (n = 1,534). The rs8040868 variant is in linkage disequilibrium with rs16969968 previously associated with COPD and altered expression of the CHRNA5 gene. A follow-up analysis for detection of expression quantitative trait loci revealed that rs8040868-C was found to be significantly associated with a decreased expression of the nearby gene cholinergic receptor, nicotinic, alpha 5 (CHRNA5) in lung tissue. CONCLUSION: Our data replicate previous result suggesting CHRNA5 as a candidate gene for COPD and rs8040868 as a risk variant for the development of COPD in the Swedish population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0309-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-11 /pmc/articles/PMC5106844/ /pubmed/27835950 http://dx.doi.org/10.1186/s12890-016-0309-y 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 Matsson, Hans Söderhäll, Cilla Einarsdottir, Elisabet Lamontagne, Maxime Gudmundsson, Sanna Backman, Helena Lindberg, Anne Rönmark, Eva Kere, Juha Sin, Don Postma, Dirkje S. Bossé, Yohan Lundbäck, Bo Klar, Joakim Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title | Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title_full | Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title_fullStr | Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title_full_unstemmed | Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title_short | Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
title_sort | targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106844/ https://www.ncbi.nlm.nih.gov/pubmed/27835950 http://dx.doi.org/10.1186/s12890-016-0309-y |
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