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Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions
Current microRNA target predictions are based on sequence information and empirically derived rules but do not make use of the expression of microRNAs and their targets. This study aimed to improve microRNA target predictions in a given biological context, using in silico predictions, microRNA and m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753644/ https://www.ncbi.nlm.nih.gov/pubmed/23771142 http://dx.doi.org/10.1093/nar/gkt525 |
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author | van Iterson, Maarten Bervoets, Sander de Meijer, Emile J. Buermans, Henk P. ’t Hoen, Peter A. C. Menezes, Renée X. Boer, Judith M. |
author_facet | van Iterson, Maarten Bervoets, Sander de Meijer, Emile J. Buermans, Henk P. ’t Hoen, Peter A. C. Menezes, Renée X. Boer, Judith M. |
author_sort | van Iterson, Maarten |
collection | PubMed |
description | Current microRNA target predictions are based on sequence information and empirically derived rules but do not make use of the expression of microRNAs and their targets. This study aimed to improve microRNA target predictions in a given biological context, using in silico predictions, microRNA and mRNA expression. We used target prediction tools to produce lists of predicted targets and used a gene set test designed to detect consistent effects of microRNAs on the joint expression of multiple targets. In a single test, association between microRNA expression and target gene set expression as well as the contribution of the individual target genes on the association are determined. The strongest negatively associated mRNAs as measured by the test were prioritized. We applied our integration method to a well-defined muscle differentiation model. Validation of our predictions in C2C12 cells confirmed predicted targets of known as well as novel muscle-related microRNAs. We further studied associations between microRNA–mRNA pairs in human prostate cancer, finding some pairs that have been recently experimentally validated by others. Using the same study, we showed the advantages of the global test over Pearson correlation and lasso. We conclude that our integrated approach successfully identifies regulated microRNAs and their targets. |
format | Online Article Text |
id | pubmed-3753644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37536442013-08-27 Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions van Iterson, Maarten Bervoets, Sander de Meijer, Emile J. Buermans, Henk P. ’t Hoen, Peter A. C. Menezes, Renée X. Boer, Judith M. Nucleic Acids Res Methods Online Current microRNA target predictions are based on sequence information and empirically derived rules but do not make use of the expression of microRNAs and their targets. This study aimed to improve microRNA target predictions in a given biological context, using in silico predictions, microRNA and mRNA expression. We used target prediction tools to produce lists of predicted targets and used a gene set test designed to detect consistent effects of microRNAs on the joint expression of multiple targets. In a single test, association between microRNA expression and target gene set expression as well as the contribution of the individual target genes on the association are determined. The strongest negatively associated mRNAs as measured by the test were prioritized. We applied our integration method to a well-defined muscle differentiation model. Validation of our predictions in C2C12 cells confirmed predicted targets of known as well as novel muscle-related microRNAs. We further studied associations between microRNA–mRNA pairs in human prostate cancer, finding some pairs that have been recently experimentally validated by others. Using the same study, we showed the advantages of the global test over Pearson correlation and lasso. We conclude that our integrated approach successfully identifies regulated microRNAs and their targets. Oxford University Press 2013-08 2013-06-14 /pmc/articles/PMC3753644/ /pubmed/23771142 http://dx.doi.org/10.1093/nar/gkt525 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online van Iterson, Maarten Bervoets, Sander de Meijer, Emile J. Buermans, Henk P. ’t Hoen, Peter A. C. Menezes, Renée X. Boer, Judith M. Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title | Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title_full | Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title_fullStr | Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title_full_unstemmed | Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title_short | Integrated analysis of microRNA and mRNA expression: adding biological significance to microRNA target predictions |
title_sort | integrated analysis of microrna and mrna expression: adding biological significance to microrna target predictions |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753644/ https://www.ncbi.nlm.nih.gov/pubmed/23771142 http://dx.doi.org/10.1093/nar/gkt525 |
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