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Survey of allele specific expression in bovine muscle
Allelic imbalance is a common phenomenon in mammals that plays an important role in gene regulation. An Allele Specific Expression (ASE) approach can be used to detect variants with a cis-regulatory effect on gene expression. In cattle, this type of study has only been done once in Holstein. In our...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414783/ https://www.ncbi.nlm.nih.gov/pubmed/30862965 http://dx.doi.org/10.1038/s41598-019-40781-6 |
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author | Guillocheau, Gabriel M. El Hou, Abdelmajid Meersseman, Cédric Esquerré, Diane Rebours, Emmanuelle Letaief, Rabia Simao, Morgane Hypolite, Nicolas Bourneuf, Emmanuelle Bruneau, Nicolas Vaiman, Anne Vander Jagt, Christy J. Chamberlain, Amanda J. Rocha, Dominique |
author_facet | Guillocheau, Gabriel M. El Hou, Abdelmajid Meersseman, Cédric Esquerré, Diane Rebours, Emmanuelle Letaief, Rabia Simao, Morgane Hypolite, Nicolas Bourneuf, Emmanuelle Bruneau, Nicolas Vaiman, Anne Vander Jagt, Christy J. Chamberlain, Amanda J. Rocha, Dominique |
author_sort | Guillocheau, Gabriel M. |
collection | PubMed |
description | Allelic imbalance is a common phenomenon in mammals that plays an important role in gene regulation. An Allele Specific Expression (ASE) approach can be used to detect variants with a cis-regulatory effect on gene expression. In cattle, this type of study has only been done once in Holstein. In our study we performed a genome-wide analysis of ASE in 19 Limousine muscle samples. We identified 5,658 ASE SNPs (Single Nucleotide Polymorphisms showing allele specific expression) in 13% of genes with detectable expression in the Longissimus thoraci muscle. Interestingly we found allelic imbalance in AOX1, PALLD and CAST genes. We also found 2,107 ASE SNPs located within genomic regions associated with meat or carcass traits. In order to identify causative cis-regulatory variants explaining ASE we searched for SNPs altering binding sites of transcription factors or microRNAs. We identified one SNP in the 3’UTR region of PRNP that could be a causal regulatory variant modifying binding sites of several miRNAs. We showed that ASE is frequent within our muscle samples. Our data could be used to elucidate the molecular mechanisms underlying gene expression imbalance. |
format | Online Article Text |
id | pubmed-6414783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64147832019-03-15 Survey of allele specific expression in bovine muscle Guillocheau, Gabriel M. El Hou, Abdelmajid Meersseman, Cédric Esquerré, Diane Rebours, Emmanuelle Letaief, Rabia Simao, Morgane Hypolite, Nicolas Bourneuf, Emmanuelle Bruneau, Nicolas Vaiman, Anne Vander Jagt, Christy J. Chamberlain, Amanda J. Rocha, Dominique Sci Rep Article Allelic imbalance is a common phenomenon in mammals that plays an important role in gene regulation. An Allele Specific Expression (ASE) approach can be used to detect variants with a cis-regulatory effect on gene expression. In cattle, this type of study has only been done once in Holstein. In our study we performed a genome-wide analysis of ASE in 19 Limousine muscle samples. We identified 5,658 ASE SNPs (Single Nucleotide Polymorphisms showing allele specific expression) in 13% of genes with detectable expression in the Longissimus thoraci muscle. Interestingly we found allelic imbalance in AOX1, PALLD and CAST genes. We also found 2,107 ASE SNPs located within genomic regions associated with meat or carcass traits. In order to identify causative cis-regulatory variants explaining ASE we searched for SNPs altering binding sites of transcription factors or microRNAs. We identified one SNP in the 3’UTR region of PRNP that could be a causal regulatory variant modifying binding sites of several miRNAs. We showed that ASE is frequent within our muscle samples. Our data could be used to elucidate the molecular mechanisms underlying gene expression imbalance. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414783/ /pubmed/30862965 http://dx.doi.org/10.1038/s41598-019-40781-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guillocheau, Gabriel M. El Hou, Abdelmajid Meersseman, Cédric Esquerré, Diane Rebours, Emmanuelle Letaief, Rabia Simao, Morgane Hypolite, Nicolas Bourneuf, Emmanuelle Bruneau, Nicolas Vaiman, Anne Vander Jagt, Christy J. Chamberlain, Amanda J. Rocha, Dominique Survey of allele specific expression in bovine muscle |
title | Survey of allele specific expression in bovine muscle |
title_full | Survey of allele specific expression in bovine muscle |
title_fullStr | Survey of allele specific expression in bovine muscle |
title_full_unstemmed | Survey of allele specific expression in bovine muscle |
title_short | Survey of allele specific expression in bovine muscle |
title_sort | survey of allele specific expression in bovine muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414783/ https://www.ncbi.nlm.nih.gov/pubmed/30862965 http://dx.doi.org/10.1038/s41598-019-40781-6 |
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