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Extracting proteins involved in disease progression using temporally connected networks

BACKGROUND: Metabolic disorders such as obesity and diabetes are diseases which develop gradually over time in an individual and through the perturbations of genes. Systematic experiments tracking disease progression at gene level are usually conducted giving a temporal microarray data. There is a n...

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Autores principales: Anand, Rajat, Sarmah, Dipanka Tanu, Chatterjee, Samrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060549/
https://www.ncbi.nlm.nih.gov/pubmed/30045727
http://dx.doi.org/10.1186/s12918-018-0600-z
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author Anand, Rajat
Sarmah, Dipanka Tanu
Chatterjee, Samrat
author_facet Anand, Rajat
Sarmah, Dipanka Tanu
Chatterjee, Samrat
author_sort Anand, Rajat
collection PubMed
description BACKGROUND: Metabolic disorders such as obesity and diabetes are diseases which develop gradually over time in an individual and through the perturbations of genes. Systematic experiments tracking disease progression at gene level are usually conducted giving a temporal microarray data. There is a need for developing methods to analyze such complex data and extract important proteins which could be involved in temporal progression of the data and hence progression of the disease. RESULTS: In the present study, we have considered a temporal microarray data from an experiment conducted to study development of obesity and diabetes in mice. We have used this data along with an available Protein-Protein Interaction network to find a network of interactions between proteins which reproduces the next time point data from previous time point data. We show that the resulting network can be mined to identify critical nodes involved in the temporal progression of perturbations. We further show that published algorithms can be applied on such connected network to mine important proteins and show an overlap between outputs from published and our algorithms. The importance of set of proteins identified was supported by literature as well as was further validated by comparing them with the positive genes dataset from OMIM database which shows significant overlap. CONCLUSIONS: The critical proteins identified from algorithms can be hypothesized to play important role in temporal progression of the data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0600-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-60605492018-07-31 Extracting proteins involved in disease progression using temporally connected networks Anand, Rajat Sarmah, Dipanka Tanu Chatterjee, Samrat BMC Syst Biol Research Article BACKGROUND: Metabolic disorders such as obesity and diabetes are diseases which develop gradually over time in an individual and through the perturbations of genes. Systematic experiments tracking disease progression at gene level are usually conducted giving a temporal microarray data. There is a need for developing methods to analyze such complex data and extract important proteins which could be involved in temporal progression of the data and hence progression of the disease. RESULTS: In the present study, we have considered a temporal microarray data from an experiment conducted to study development of obesity and diabetes in mice. We have used this data along with an available Protein-Protein Interaction network to find a network of interactions between proteins which reproduces the next time point data from previous time point data. We show that the resulting network can be mined to identify critical nodes involved in the temporal progression of perturbations. We further show that published algorithms can be applied on such connected network to mine important proteins and show an overlap between outputs from published and our algorithms. The importance of set of proteins identified was supported by literature as well as was further validated by comparing them with the positive genes dataset from OMIM database which shows significant overlap. CONCLUSIONS: The critical proteins identified from algorithms can be hypothesized to play important role in temporal progression of the data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0600-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-25 /pmc/articles/PMC6060549/ /pubmed/30045727 http://dx.doi.org/10.1186/s12918-018-0600-z Text en © The Author(s). 2018 Open AccessThis 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
Anand, Rajat
Sarmah, Dipanka Tanu
Chatterjee, Samrat
Extracting proteins involved in disease progression using temporally connected networks
title Extracting proteins involved in disease progression using temporally connected networks
title_full Extracting proteins involved in disease progression using temporally connected networks
title_fullStr Extracting proteins involved in disease progression using temporally connected networks
title_full_unstemmed Extracting proteins involved in disease progression using temporally connected networks
title_short Extracting proteins involved in disease progression using temporally connected networks
title_sort extracting proteins involved in disease progression using temporally connected networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060549/
https://www.ncbi.nlm.nih.gov/pubmed/30045727
http://dx.doi.org/10.1186/s12918-018-0600-z
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