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Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption

To identify brain transcriptional networks that may predispose an animal to consume alcohol, we used weighted gene coexpression network analysis (WGCNA). Candidate coexpression modules are those with an eigengene expression level that correlates significantly with the level of alcohol consumption ac...

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Autores principales: Vanderlinden, Lauren A., Saba, Laura M., Kechris, Katerina, Miles, Michael F., Hoffman, Paula L., Tabakoff, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720886/
https://www.ncbi.nlm.nih.gov/pubmed/23894363
http://dx.doi.org/10.1371/journal.pone.0068878
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author Vanderlinden, Lauren A.
Saba, Laura M.
Kechris, Katerina
Miles, Michael F.
Hoffman, Paula L.
Tabakoff, Boris
author_facet Vanderlinden, Lauren A.
Saba, Laura M.
Kechris, Katerina
Miles, Michael F.
Hoffman, Paula L.
Tabakoff, Boris
author_sort Vanderlinden, Lauren A.
collection PubMed
description To identify brain transcriptional networks that may predispose an animal to consume alcohol, we used weighted gene coexpression network analysis (WGCNA). Candidate coexpression modules are those with an eigengene expression level that correlates significantly with the level of alcohol consumption across a panel of BXD recombinant inbred mouse strains, and that share a genomic region that regulates the module transcript expression levels (mQTL) with a genomic region that regulates alcohol consumption (bQTL). To address a controversy regarding utility of gene expression profiles from whole brain, vs specific brain regions, as indicators of the relationship of gene expression to phenotype, we compared candidate coexpression modules from whole brain gene expression data (gathered with Affymetrix 430 v2 arrays in the Colorado laboratories) and from gene expression data from 6 brain regions (nucleus accumbens (NA); prefrontal cortex (PFC); ventral tegmental area (VTA); striatum (ST); hippocampus (HP); cerebellum (CB)) available from GeneNetwork. The candidate modules were used to construct candidate eigengene networks across brain regions, resulting in three “meta-modules”, composed of candidate modules from two or more brain regions (NA, PFC, ST, VTA) and whole brain. To mitigate the potential influence of chromosomal location of transcripts and cis-eQTLs in linkage disequilibrium, we calculated a semi-partial correlation of the transcripts in the meta-modules with alcohol consumption conditional on the transcripts' cis-eQTLs. The function of transcripts that retained the correlation with the phenotype after correction for the strong genetic influence, implicates processes of protein metabolism in the ER and Golgi as influencing susceptibility to variation in alcohol consumption. Integration of these data with human GWAS provides further information on the function of polymorphisms associated with alcohol-related traits.
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spelling pubmed-37208862013-07-26 Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption Vanderlinden, Lauren A. Saba, Laura M. Kechris, Katerina Miles, Michael F. Hoffman, Paula L. Tabakoff, Boris PLoS One Research Article To identify brain transcriptional networks that may predispose an animal to consume alcohol, we used weighted gene coexpression network analysis (WGCNA). Candidate coexpression modules are those with an eigengene expression level that correlates significantly with the level of alcohol consumption across a panel of BXD recombinant inbred mouse strains, and that share a genomic region that regulates the module transcript expression levels (mQTL) with a genomic region that regulates alcohol consumption (bQTL). To address a controversy regarding utility of gene expression profiles from whole brain, vs specific brain regions, as indicators of the relationship of gene expression to phenotype, we compared candidate coexpression modules from whole brain gene expression data (gathered with Affymetrix 430 v2 arrays in the Colorado laboratories) and from gene expression data from 6 brain regions (nucleus accumbens (NA); prefrontal cortex (PFC); ventral tegmental area (VTA); striatum (ST); hippocampus (HP); cerebellum (CB)) available from GeneNetwork. The candidate modules were used to construct candidate eigengene networks across brain regions, resulting in three “meta-modules”, composed of candidate modules from two or more brain regions (NA, PFC, ST, VTA) and whole brain. To mitigate the potential influence of chromosomal location of transcripts and cis-eQTLs in linkage disequilibrium, we calculated a semi-partial correlation of the transcripts in the meta-modules with alcohol consumption conditional on the transcripts' cis-eQTLs. The function of transcripts that retained the correlation with the phenotype after correction for the strong genetic influence, implicates processes of protein metabolism in the ER and Golgi as influencing susceptibility to variation in alcohol consumption. Integration of these data with human GWAS provides further information on the function of polymorphisms associated with alcohol-related traits. Public Library of Science 2013-07-23 /pmc/articles/PMC3720886/ /pubmed/23894363 http://dx.doi.org/10.1371/journal.pone.0068878 Text en © 2013 Vanderlinden 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
Vanderlinden, Lauren A.
Saba, Laura M.
Kechris, Katerina
Miles, Michael F.
Hoffman, Paula L.
Tabakoff, Boris
Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title_full Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title_fullStr Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title_full_unstemmed Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title_short Whole Brain and Brain Regional Coexpression Network Interactions Associated with Predisposition to Alcohol Consumption
title_sort whole brain and brain regional coexpression network interactions associated with predisposition to alcohol consumption
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720886/
https://www.ncbi.nlm.nih.gov/pubmed/23894363
http://dx.doi.org/10.1371/journal.pone.0068878
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