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Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection
BACKGROUND: The immune response to viral infection is a temporal process, represented by a dynamic and complex network of gene and protein interactions. Here, we present a reverse engineering strategy aimed at capturing the temporal evolution of the underlying Gene Regulatory Networks (GRN). The pro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219564/ https://www.ncbi.nlm.nih.gov/pubmed/22017961 http://dx.doi.org/10.1186/2043-9113-1-27 |
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author | Dimitrakopoulou, Konstantina Tsimpouris, Charalampos Papadopoulos, George Pommerenke, Claudia Wilk, Esther Sgarbas, Kyriakos N Schughart, Klaus Bezerianos, Anastasios |
author_facet | Dimitrakopoulou, Konstantina Tsimpouris, Charalampos Papadopoulos, George Pommerenke, Claudia Wilk, Esther Sgarbas, Kyriakos N Schughart, Klaus Bezerianos, Anastasios |
author_sort | Dimitrakopoulou, Konstantina |
collection | PubMed |
description | BACKGROUND: The immune response to viral infection is a temporal process, represented by a dynamic and complex network of gene and protein interactions. Here, we present a reverse engineering strategy aimed at capturing the temporal evolution of the underlying Gene Regulatory Networks (GRN). The proposed approach will be an enabling step towards comprehending the dynamic behavior of gene regulation circuitry and mapping the network structure transitions in response to pathogen stimuli. RESULTS: We applied the Time Varying Dynamic Bayesian Network (TV-DBN) method for reconstructing the gene regulatory interactions based on time series gene expression data for the mouse C57BL/6J inbred strain after infection with influenza A H1N1 (PR8) virus. Initially, 3500 differentially expressed genes were clustered with the use of k-means algorithm. Next, the successive in time GRNs were built over the expression profiles of cluster centroids. Finally, the identified GRNs were examined with several topological metrics and available protein-protein and protein-DNA interaction data, transcription factor and KEGG pathway data. CONCLUSIONS: Our results elucidate the potential of TV-DBN approach in providing valuable insights into the temporal rewiring of the lung transcriptome in response to H1N1 virus. |
format | Online Article Text |
id | pubmed-3219564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32195642011-11-18 Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection Dimitrakopoulou, Konstantina Tsimpouris, Charalampos Papadopoulos, George Pommerenke, Claudia Wilk, Esther Sgarbas, Kyriakos N Schughart, Klaus Bezerianos, Anastasios J Clin Bioinforma Methodology BACKGROUND: The immune response to viral infection is a temporal process, represented by a dynamic and complex network of gene and protein interactions. Here, we present a reverse engineering strategy aimed at capturing the temporal evolution of the underlying Gene Regulatory Networks (GRN). The proposed approach will be an enabling step towards comprehending the dynamic behavior of gene regulation circuitry and mapping the network structure transitions in response to pathogen stimuli. RESULTS: We applied the Time Varying Dynamic Bayesian Network (TV-DBN) method for reconstructing the gene regulatory interactions based on time series gene expression data for the mouse C57BL/6J inbred strain after infection with influenza A H1N1 (PR8) virus. Initially, 3500 differentially expressed genes were clustered with the use of k-means algorithm. Next, the successive in time GRNs were built over the expression profiles of cluster centroids. Finally, the identified GRNs were examined with several topological metrics and available protein-protein and protein-DNA interaction data, transcription factor and KEGG pathway data. CONCLUSIONS: Our results elucidate the potential of TV-DBN approach in providing valuable insights into the temporal rewiring of the lung transcriptome in response to H1N1 virus. BioMed Central 2011-10-21 /pmc/articles/PMC3219564/ /pubmed/22017961 http://dx.doi.org/10.1186/2043-9113-1-27 Text en Copyright ©2011 Dimitrakopoulou 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 | Methodology Dimitrakopoulou, Konstantina Tsimpouris, Charalampos Papadopoulos, George Pommerenke, Claudia Wilk, Esther Sgarbas, Kyriakos N Schughart, Klaus Bezerianos, Anastasios Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title | Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title_full | Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title_fullStr | Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title_full_unstemmed | Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title_short | Dynamic gene network reconstruction from gene expression data in mice after influenza A (H1N1) infection |
title_sort | dynamic gene network reconstruction from gene expression data in mice after influenza a (h1n1) infection |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219564/ https://www.ncbi.nlm.nih.gov/pubmed/22017961 http://dx.doi.org/10.1186/2043-9113-1-27 |
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