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Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels
BACKGROUND: CCL16 is a chemokine predominantly expressed in the liver, but is also found in the blood and brain, and is known to play important roles in immune response and angiogenesis. Little is known about the gene’s regulation. METHODS: Here, we test for potential causal SNPs that affect CCL16 p...
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/PMC4943476/ https://www.ncbi.nlm.nih.gov/pubmed/27357396 http://dx.doi.org/10.1186/s12864-016-2788-x |
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author | Ebbert, Mark T. W. Staley, Lyndsay A. Parker, Joshua Parker, Sheradyn Bailey, Matthew Ridge, Perry G. Goate, Alison M. Kauwe, John S. K. |
author_facet | Ebbert, Mark T. W. Staley, Lyndsay A. Parker, Joshua Parker, Sheradyn Bailey, Matthew Ridge, Perry G. Goate, Alison M. Kauwe, John S. K. |
author_sort | Ebbert, Mark T. W. |
collection | PubMed |
description | BACKGROUND: CCL16 is a chemokine predominantly expressed in the liver, but is also found in the blood and brain, and is known to play important roles in immune response and angiogenesis. Little is known about the gene’s regulation. METHODS: Here, we test for potential causal SNPs that affect CCL16 protein levels in both blood plasma and cerebrospinal fluid in a genome-wide association study across two datasets. We then use METAL to performed meta-analyses with a significance threshold of p < 5x10(−8). We removed SNPs where the direction of the effect was different between the two datasets. RESULTS: We identify 10 SNPs associated with increased CCL16 protein levels in both biological fluids. CONCLUSIONS: Our results will help understand CCL16’s regulation, allowing researchers to better understand the gene’s effects on human health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2788-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4943476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49434762016-07-20 Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels Ebbert, Mark T. W. Staley, Lyndsay A. Parker, Joshua Parker, Sheradyn Bailey, Matthew Ridge, Perry G. Goate, Alison M. Kauwe, John S. K. BMC Genomics Research BACKGROUND: CCL16 is a chemokine predominantly expressed in the liver, but is also found in the blood and brain, and is known to play important roles in immune response and angiogenesis. Little is known about the gene’s regulation. METHODS: Here, we test for potential causal SNPs that affect CCL16 protein levels in both blood plasma and cerebrospinal fluid in a genome-wide association study across two datasets. We then use METAL to performed meta-analyses with a significance threshold of p < 5x10(−8). We removed SNPs where the direction of the effect was different between the two datasets. RESULTS: We identify 10 SNPs associated with increased CCL16 protein levels in both biological fluids. CONCLUSIONS: Our results will help understand CCL16’s regulation, allowing researchers to better understand the gene’s effects on human health. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2788-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-29 /pmc/articles/PMC4943476/ /pubmed/27357396 http://dx.doi.org/10.1186/s12864-016-2788-x 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 Ebbert, Mark T. W. Staley, Lyndsay A. Parker, Joshua Parker, Sheradyn Bailey, Matthew Ridge, Perry G. Goate, Alison M. Kauwe, John S. K. Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title | Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title_full | Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title_fullStr | Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title_full_unstemmed | Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title_short | Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels |
title_sort | variants in ccl16 are associated with blood plasma and cerebrospinal fluid ccl16 protein levels |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943476/ https://www.ncbi.nlm.nih.gov/pubmed/27357396 http://dx.doi.org/10.1186/s12864-016-2788-x |
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