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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Series: | PLoS Computational Biology |
Online Access: | https://doi.org/10.1371/journal.pcbi.1004504 |
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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 |
work_keys_str_mv |
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1714668017421385728 |