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Detecting microRNA activity from gene expression data
BACKGROUND: MicroRNAs (miRNAs) are non-coding RNAs that regulate gene expression by binding to the messenger RNA (mRNA) of protein coding genes. They control gene expression by either inhibiting translation or inducing mRNA degradation. A number of computational techniques have been developed to ide...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885376/ https://www.ncbi.nlm.nih.gov/pubmed/20482775 http://dx.doi.org/10.1186/1471-2105-11-257 |
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author | Madden, Stephen F Carpenter, Susan B Jeffery, Ian B Björkbacka, Harry Fitzgerald, Katherine A O'Neill, Luke A Higgins, Desmond G |
author_facet | Madden, Stephen F Carpenter, Susan B Jeffery, Ian B Björkbacka, Harry Fitzgerald, Katherine A O'Neill, Luke A Higgins, Desmond G |
author_sort | Madden, Stephen F |
collection | PubMed |
description | BACKGROUND: MicroRNAs (miRNAs) are non-coding RNAs that regulate gene expression by binding to the messenger RNA (mRNA) of protein coding genes. They control gene expression by either inhibiting translation or inducing mRNA degradation. A number of computational techniques have been developed to identify the targets of miRNAs. In this study we used predicted miRNA-gene interactions to analyse mRNA gene expression microarray data to predict miRNAs associated with particular diseases or conditions. RESULTS: Here we combine correspondence analysis, between group analysis and co-inertia analysis (CIA) to determine which miRNAs are associated with differences in gene expression levels in microarray data sets. Using a database of miRNA target predictions from TargetScan, TargetScanS, PicTar4way PicTar5way, and miRanda and combining these data with gene expression levels from sets of microarrays, this method produces a ranked list of miRNAs associated with a specified split in samples. We applied this to three different microarray datasets, a papillary thyroid carcinoma dataset, an in-house dataset of lipopolysaccharide treated mouse macrophages, and a multi-tissue dataset. In each case we were able to identified miRNAs of biological importance. CONCLUSIONS: We describe a technique to integrate gene expression data and miRNA target predictions from multiple sources. |
format | Text |
id | pubmed-2885376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28853762010-06-15 Detecting microRNA activity from gene expression data Madden, Stephen F Carpenter, Susan B Jeffery, Ian B Björkbacka, Harry Fitzgerald, Katherine A O'Neill, Luke A Higgins, Desmond G BMC Bioinformatics Research article BACKGROUND: MicroRNAs (miRNAs) are non-coding RNAs that regulate gene expression by binding to the messenger RNA (mRNA) of protein coding genes. They control gene expression by either inhibiting translation or inducing mRNA degradation. A number of computational techniques have been developed to identify the targets of miRNAs. In this study we used predicted miRNA-gene interactions to analyse mRNA gene expression microarray data to predict miRNAs associated with particular diseases or conditions. RESULTS: Here we combine correspondence analysis, between group analysis and co-inertia analysis (CIA) to determine which miRNAs are associated with differences in gene expression levels in microarray data sets. Using a database of miRNA target predictions from TargetScan, TargetScanS, PicTar4way PicTar5way, and miRanda and combining these data with gene expression levels from sets of microarrays, this method produces a ranked list of miRNAs associated with a specified split in samples. We applied this to three different microarray datasets, a papillary thyroid carcinoma dataset, an in-house dataset of lipopolysaccharide treated mouse macrophages, and a multi-tissue dataset. In each case we were able to identified miRNAs of biological importance. CONCLUSIONS: We describe a technique to integrate gene expression data and miRNA target predictions from multiple sources. BioMed Central 2010-05-18 /pmc/articles/PMC2885376/ /pubmed/20482775 http://dx.doi.org/10.1186/1471-2105-11-257 Text en Copyright ©2010 Madden et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research article Madden, Stephen F Carpenter, Susan B Jeffery, Ian B Björkbacka, Harry Fitzgerald, Katherine A O'Neill, Luke A Higgins, Desmond G Detecting microRNA activity from gene expression data |
title | Detecting microRNA activity from gene expression data |
title_full | Detecting microRNA activity from gene expression data |
title_fullStr | Detecting microRNA activity from gene expression data |
title_full_unstemmed | Detecting microRNA activity from gene expression data |
title_short | Detecting microRNA activity from gene expression data |
title_sort | detecting microrna activity from gene expression data |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885376/ https://www.ncbi.nlm.nih.gov/pubmed/20482775 http://dx.doi.org/10.1186/1471-2105-11-257 |
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