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Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse
BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that bind messenger RNAs and promote their degradation or repress their translation. There is increasing evidence of miRNAs playing an important role in alcohol related disorders. However, the role of miRNAs as mediators of the genetic effect...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114181/ https://www.ncbi.nlm.nih.gov/pubmed/30157779 http://dx.doi.org/10.1186/s12864-018-5004-3 |
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author | Rudra, Pratyaydipta Shi, Wen J. Russell, Pamela Vestal, Brian Tabakoff, Boris Hoffman, Paula Kechris, Katerina Saba, Laura |
author_facet | Rudra, Pratyaydipta Shi, Wen J. Russell, Pamela Vestal, Brian Tabakoff, Boris Hoffman, Paula Kechris, Katerina Saba, Laura |
author_sort | Rudra, Pratyaydipta |
collection | PubMed |
description | BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that bind messenger RNAs and promote their degradation or repress their translation. There is increasing evidence of miRNAs playing an important role in alcohol related disorders. However, the role of miRNAs as mediators of the genetic effect on alcohol phenotypes is not fully understood. We conducted a high-throughput sequencing study to measure miRNA expression levels in alcohol naïve animals in the LXS panel of recombinant inbred (RI) mouse strains. We then combined the sequencing data with genotype data, microarry gene expression data, and data on alcohol-related behavioral phenotypes such as ’Drinking in the dark’, ’Sleep time’, and ’Low dose activation’ from the same RI panel. SNP-miRNA-gene triplets with strong association within the triplet that were also associated with one of the 4 alcohol phenotypes were selected and a Bayesian network analysis was used to aggregate results into a directed network model. RESULTS: We found several triplets with strong association within the triplet that were also associated with one of the alcohol phenotypes. The Bayesian network analysis found two networks where a miRNA mediates the genetic effect on the alcohol phenotype. The miRNAs were found to influence the expression of protein-coding genes, which in turn influences the quantitative phenotypes. The pathways in which these genes are enriched have been previously associated with alcohol-related traits. CONCLUSION: This work enhances association studies by identifying miRNAs that may be mediating the association between genetic markers (SNPs) and the alcohol phenotypes. It suggests a mechanism of how genetic variants are affecting traits of interest through the modification of miRNA expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5004-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6114181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61141812018-09-04 Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse Rudra, Pratyaydipta Shi, Wen J. Russell, Pamela Vestal, Brian Tabakoff, Boris Hoffman, Paula Kechris, Katerina Saba, Laura BMC Genomics Research Article BACKGROUND: MicroRNAs (miRNAs) are small non-coding RNAs that bind messenger RNAs and promote their degradation or repress their translation. There is increasing evidence of miRNAs playing an important role in alcohol related disorders. However, the role of miRNAs as mediators of the genetic effect on alcohol phenotypes is not fully understood. We conducted a high-throughput sequencing study to measure miRNA expression levels in alcohol naïve animals in the LXS panel of recombinant inbred (RI) mouse strains. We then combined the sequencing data with genotype data, microarry gene expression data, and data on alcohol-related behavioral phenotypes such as ’Drinking in the dark’, ’Sleep time’, and ’Low dose activation’ from the same RI panel. SNP-miRNA-gene triplets with strong association within the triplet that were also associated with one of the 4 alcohol phenotypes were selected and a Bayesian network analysis was used to aggregate results into a directed network model. RESULTS: We found several triplets with strong association within the triplet that were also associated with one of the alcohol phenotypes. The Bayesian network analysis found two networks where a miRNA mediates the genetic effect on the alcohol phenotype. The miRNAs were found to influence the expression of protein-coding genes, which in turn influences the quantitative phenotypes. The pathways in which these genes are enriched have been previously associated with alcohol-related traits. CONCLUSION: This work enhances association studies by identifying miRNAs that may be mediating the association between genetic markers (SNPs) and the alcohol phenotypes. It suggests a mechanism of how genetic variants are affecting traits of interest through the modification of miRNA expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5004-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-29 /pmc/articles/PMC6114181/ /pubmed/30157779 http://dx.doi.org/10.1186/s12864-018-5004-3 Text en © The Author(s) 2018 Open Access This 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 Rudra, Pratyaydipta Shi, Wen J. Russell, Pamela Vestal, Brian Tabakoff, Boris Hoffman, Paula Kechris, Katerina Saba, Laura Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title | Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title_full | Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title_fullStr | Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title_full_unstemmed | Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title_short | Predictive modeling of miRNA-mediated predisposition to alcohol-related phenotypes in mouse |
title_sort | predictive modeling of mirna-mediated predisposition to alcohol-related phenotypes in mouse |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114181/ https://www.ncbi.nlm.nih.gov/pubmed/30157779 http://dx.doi.org/10.1186/s12864-018-5004-3 |
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