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Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes
Glucocorticoids (GCs) mediate physiological responses to environmental stress and are commonly used as pharmaceuticals. GCs act primarily through the GC receptor (GR, a transcription factor). Despite their clear biomedical importance, little is known about the genetic architecture of variation in GC...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131293/ https://www.ncbi.nlm.nih.gov/pubmed/21750684 http://dx.doi.org/10.1371/journal.pgen.1002162 |
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author | Maranville, Joseph C. Luca, Francesca Richards, Allison L. Wen, Xiaoquan Witonsky, David B. Baxter, Shaneen Stephens, Matthew Di Rienzo, Anna |
author_facet | Maranville, Joseph C. Luca, Francesca Richards, Allison L. Wen, Xiaoquan Witonsky, David B. Baxter, Shaneen Stephens, Matthew Di Rienzo, Anna |
author_sort | Maranville, Joseph C. |
collection | PubMed |
description | Glucocorticoids (GCs) mediate physiological responses to environmental stress and are commonly used as pharmaceuticals. GCs act primarily through the GC receptor (GR, a transcription factor). Despite their clear biomedical importance, little is known about the genetic architecture of variation in GC response. Here we provide an initial assessment of variability in the cellular response to GC treatment by profiling gene expression and protein secretion in 114 EBV-transformed B lymphocytes of African and European ancestry. We found that genetic variation affects the response of nearby genes and exhibits distinctive patterns of genotype-treatment interactions, with genotypic effects evident in either only GC-treated or only control-treated conditions. Using a novel statistical framework, we identified interactions that influence the expression of 26 genes known to play central roles in GC-related pathways (e.g. NQO1, AIRE, and SGK1) and that influence the secretion of IL6. |
format | Online Article Text |
id | pubmed-3131293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31312932011-07-12 Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes Maranville, Joseph C. Luca, Francesca Richards, Allison L. Wen, Xiaoquan Witonsky, David B. Baxter, Shaneen Stephens, Matthew Di Rienzo, Anna PLoS Genet Research Article Glucocorticoids (GCs) mediate physiological responses to environmental stress and are commonly used as pharmaceuticals. GCs act primarily through the GC receptor (GR, a transcription factor). Despite their clear biomedical importance, little is known about the genetic architecture of variation in GC response. Here we provide an initial assessment of variability in the cellular response to GC treatment by profiling gene expression and protein secretion in 114 EBV-transformed B lymphocytes of African and European ancestry. We found that genetic variation affects the response of nearby genes and exhibits distinctive patterns of genotype-treatment interactions, with genotypic effects evident in either only GC-treated or only control-treated conditions. Using a novel statistical framework, we identified interactions that influence the expression of 26 genes known to play central roles in GC-related pathways (e.g. NQO1, AIRE, and SGK1) and that influence the secretion of IL6. Public Library of Science 2011-07-07 /pmc/articles/PMC3131293/ /pubmed/21750684 http://dx.doi.org/10.1371/journal.pgen.1002162 Text en Maranville et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Maranville, Joseph C. Luca, Francesca Richards, Allison L. Wen, Xiaoquan Witonsky, David B. Baxter, Shaneen Stephens, Matthew Di Rienzo, Anna Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title | Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title_full | Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title_fullStr | Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title_full_unstemmed | Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title_short | Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes |
title_sort | interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131293/ https://www.ncbi.nlm.nih.gov/pubmed/21750684 http://dx.doi.org/10.1371/journal.pgen.1002162 |
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