Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.

Human gene regulatory networks (GRN) can be difficult to interpret due to a tangle of edges interconnecting thousands of genes. We constructed a general human GRN from extensive transcription factor and microRNA target data obtained from public databases. In a subnetwork of this GRN that is active d...

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Main Authors: Vipin Narang, Muhamad Azfar Ramli, Amit Singhal, Pavanish Kumar, Gennaro de Libero, Michael Poidinger, Christopher Monterola
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1004504
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spelling doaj-4636c259c95c43e2af1c2101047ecb082021-04-21T14:59:40ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582015-01-01119e100450410.1371/journal.pcbi.1004504Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.Vipin NarangMuhamad Azfar RamliAmit SinghalPavanish KumarGennaro de LiberoMichael PoidingerChristopher MonterolaHuman gene regulatory networks (GRN) can be difficult to interpret due to a tangle of edges interconnecting thousands of genes. We constructed a general human GRN from extensive transcription factor and microRNA target data obtained from public databases. In a subnetwork of this GRN that is active during estrogen stimulation of MCF-7 breast cancer cells, we benchmarked automated algorithms for identifying core regulatory genes (transcription factors and microRNAs). Among these algorithms, we identified K-core decomposition, pagerank and betweenness centrality algorithms as the most effective for discovering core regulatory genes in the network evaluated based on previously known roles of these genes in MCF-7 biology as well as in their ability to explain the up or down expression status of up to 70% of the remaining genes. Finally, we validated the use of K-core algorithm for organizing the GRN in an easier to interpret layered hierarchy where more influential regulatory genes percolate towards the inner layers. The integrated human gene and miRNA network and software used in this study are provided as supplementary materials (S1 Data) accompanying this manuscript.https://doi.org/10.1371/journal.pcbi.1004504
collection DOAJ
language English
format Article
sources DOAJ
author Vipin Narang
Muhamad Azfar Ramli
Amit Singhal
Pavanish Kumar
Gennaro de Libero
Michael Poidinger
Christopher Monterola
spellingShingle Vipin Narang
Muhamad Azfar Ramli
Amit Singhal
Pavanish Kumar
Gennaro de Libero
Michael Poidinger
Christopher Monterola
Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
PLoS Computational Biology
author_facet Vipin Narang
Muhamad Azfar Ramli
Amit Singhal
Pavanish Kumar
Gennaro de Libero
Michael Poidinger
Christopher Monterola
author_sort Vipin Narang
title Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
title_short Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
title_full Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
title_fullStr Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
title_full_unstemmed Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks.
title_sort automated identification of core regulatory genes in human gene regulatory networks.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2015-01-01
description Human gene regulatory networks (GRN) can be difficult to interpret due to a tangle of edges interconnecting thousands of genes. We constructed a general human GRN from extensive transcription factor and microRNA target data obtained from public databases. In a subnetwork of this GRN that is active during estrogen stimulation of MCF-7 breast cancer cells, we benchmarked automated algorithms for identifying core regulatory genes (transcription factors and microRNAs). Among these algorithms, we identified K-core decomposition, pagerank and betweenness centrality algorithms as the most effective for discovering core regulatory genes in the network evaluated based on previously known roles of these genes in MCF-7 biology as well as in their ability to explain the up or down expression status of up to 70% of the remaining genes. Finally, we validated the use of K-core algorithm for organizing the GRN in an easier to interpret layered hierarchy where more influential regulatory genes percolate towards the inner layers. The integrated human gene and miRNA network and software used in this study are provided as supplementary materials (S1 Data) accompanying this manuscript.
url https://doi.org/10.1371/journal.pcbi.1004504
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