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Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks
BACKGROUND: Network co-regulated modules are believed to have the functionality of packaging multiple biological entities, and can thus be assumed to coordinate many biological functions in their network neighbouring regions. RESULTS: Here, we weighted edges of a human protein interaction network an...
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/PMC2914056/ https://www.ncbi.nlm.nih.gov/pubmed/20649980 http://dx.doi.org/10.1186/1471-2105-11-392 |
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author | Chen, Lina Wang, Hong Zhang, Liangcai Li, Wan Wang, Qian Shang, Yukui He, Yuehan He, Weiming Li, Xu Tai, Jingxie Li, Xia |
author_facet | Chen, Lina Wang, Hong Zhang, Liangcai Li, Wan Wang, Qian Shang, Yukui He, Yuehan He, Weiming Li, Xu Tai, Jingxie Li, Xia |
author_sort | Chen, Lina |
collection | PubMed |
description | BACKGROUND: Network co-regulated modules are believed to have the functionality of packaging multiple biological entities, and can thus be assumed to coordinate many biological functions in their network neighbouring regions. RESULTS: Here, we weighted edges of a human protein interaction network and a transcriptional regulatory network to construct an integrated network, and introduce a probabilistic model and a bipartite graph framework to exploit human co-regulated modules and uncover their specific features in packaging different biological entities (genes, protein complexes or metabolic pathways). Finally, we identified 96 human co-regulated modules based on this method, and evaluate its effectiveness by comparing it with four other methods. CONCLUSIONS: Dysfunctions in co-regulated interactions often occur in the development of cancer. Therefore, we focussed on an example co-regulated module and found that it could integrate a number of cancer-related genes. This was extended to causal dysfunctions of some complexes maintained by several physically interacting proteins, thus coordinating several metabolic pathways that directly underlie cancer. |
format | Text |
id | pubmed-2914056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29140562010-08-03 Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks Chen, Lina Wang, Hong Zhang, Liangcai Li, Wan Wang, Qian Shang, Yukui He, Yuehan He, Weiming Li, Xu Tai, Jingxie Li, Xia BMC Bioinformatics Research Article BACKGROUND: Network co-regulated modules are believed to have the functionality of packaging multiple biological entities, and can thus be assumed to coordinate many biological functions in their network neighbouring regions. RESULTS: Here, we weighted edges of a human protein interaction network and a transcriptional regulatory network to construct an integrated network, and introduce a probabilistic model and a bipartite graph framework to exploit human co-regulated modules and uncover their specific features in packaging different biological entities (genes, protein complexes or metabolic pathways). Finally, we identified 96 human co-regulated modules based on this method, and evaluate its effectiveness by comparing it with four other methods. CONCLUSIONS: Dysfunctions in co-regulated interactions often occur in the development of cancer. Therefore, we focussed on an example co-regulated module and found that it could integrate a number of cancer-related genes. This was extended to causal dysfunctions of some complexes maintained by several physically interacting proteins, thus coordinating several metabolic pathways that directly underlie cancer. BioMed Central 2010-07-22 /pmc/articles/PMC2914056/ /pubmed/20649980 http://dx.doi.org/10.1186/1471-2105-11-392 Text en Copyright ©2010 Chen 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 Chen, Lina Wang, Hong Zhang, Liangcai Li, Wan Wang, Qian Shang, Yukui He, Yuehan He, Weiming Li, Xu Tai, Jingxie Li, Xia Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title | Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title_full | Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title_fullStr | Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title_full_unstemmed | Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title_short | Uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
title_sort | uncovering packaging features of co-regulated modules based on human protein interaction and transcriptional regulatory networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914056/ https://www.ncbi.nlm.nih.gov/pubmed/20649980 http://dx.doi.org/10.1186/1471-2105-11-392 |
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