Information Flow Analysis of Interactome Networks

Recent studies of cellular networks have revealed modular organizations of genes and proteins. For example, in interactome networks, a module refers to a group of interacting proteins that form molecular complexes and/or biochemical pathways and together mediate a biological process. However, it is...

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Main Authors: Liu, Kesheng, Ge, Hui, Ross, Brian Christopher, Missiuro, Patrycja Vasilyev, Zhao, Guoyan, Liu, Jun S., Zou, Lihua
Other Authors: Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
Format: Article
Language:en_US
Published: Public Library of Science 2010
Online Access:http://hdl.handle.net/1721.1/54708
https://orcid.org/0000-0003-2432-4678
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author Liu, Kesheng
Ge, Hui
Ross, Brian Christopher
Missiuro, Patrycja Vasilyev
Zhao, Guoyan
Liu, Jun S.
Zou, Lihua
author2 Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
author_facet Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
Liu, Kesheng
Ge, Hui
Ross, Brian Christopher
Missiuro, Patrycja Vasilyev
Zhao, Guoyan
Liu, Jun S.
Zou, Lihua
author_sort Liu, Kesheng
collection MIT
description Recent studies of cellular networks have revealed modular organizations of genes and proteins. For example, in interactome networks, a module refers to a group of interacting proteins that form molecular complexes and/or biochemical pathways and together mediate a biological process. However, it is still poorly understood how biological information is transmitted between different modules. We have developed information flow analysis, a new computational approach that identifies proteins central to the transmission of biological information throughout the network. In the information flow analysis, we represent an interactome network as an electrical circuit, where interactions are modeled as resistors and proteins as interconnecting junctions. Construing the propagation of biological signals as flow of electrical current, our method calculates an information flow score for every protein. Unlike previous metrics of network centrality such as degree or betweenness that only consider topological features, our approach incorporates confidence scores of protein–protein interactions and automatically considers all possible paths in a network when evaluating the importance of each protein. We apply our method to the interactome networks of Saccharomyces cerevisiae and Caenorhabditis elegans. We find that the likelihood of observing lethality and pleiotropy when a protein is eliminated is positively correlated with the protein's information flow score. Even among proteins of low degree or low betweenness, high information scores serve as a strong predictor of loss-of-function lethality or pleiotropy. The correlation between information flow scores and phenotypes supports our hypothesis that the proteins of high information flow reside in central positions in interactome networks. We also show that the ranks of information flow scores are more consistent than that of betweenness when a large amount of noisy data is added to an interactome. Finally, we combine gene expression data with interaction data in C. elegans and construct an interactome network for muscle-specific genes. We find that genes that rank high in terms of information flow in the muscle interactome network but not in the entire network tend to play important roles in muscle function. This framework for studying tissue-specific networks by the information flow model can be applied to other tissues and other organisms as well.
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spelling mit-1721.1/547082022-09-29T10:50:02Z Information Flow Analysis of Interactome Networks Liu, Kesheng Ge, Hui Ross, Brian Christopher Missiuro, Patrycja Vasilyev Zhao, Guoyan Liu, Jun S. Zou, Lihua Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory Massachusetts Institute of Technology. Department of Physics Whitehead Institute for Biomedical Research Missiuro, Patrycja Vasilyev Liu, Kesheng Ge, Hui Ross, Brian Christopher Missiuro, Patrycja Vasilyev Recent studies of cellular networks have revealed modular organizations of genes and proteins. For example, in interactome networks, a module refers to a group of interacting proteins that form molecular complexes and/or biochemical pathways and together mediate a biological process. However, it is still poorly understood how biological information is transmitted between different modules. We have developed information flow analysis, a new computational approach that identifies proteins central to the transmission of biological information throughout the network. In the information flow analysis, we represent an interactome network as an electrical circuit, where interactions are modeled as resistors and proteins as interconnecting junctions. Construing the propagation of biological signals as flow of electrical current, our method calculates an information flow score for every protein. Unlike previous metrics of network centrality such as degree or betweenness that only consider topological features, our approach incorporates confidence scores of protein–protein interactions and automatically considers all possible paths in a network when evaluating the importance of each protein. We apply our method to the interactome networks of Saccharomyces cerevisiae and Caenorhabditis elegans. We find that the likelihood of observing lethality and pleiotropy when a protein is eliminated is positively correlated with the protein's information flow score. Even among proteins of low degree or low betweenness, high information scores serve as a strong predictor of loss-of-function lethality or pleiotropy. The correlation between information flow scores and phenotypes supports our hypothesis that the proteins of high information flow reside in central positions in interactome networks. We also show that the ranks of information flow scores are more consistent than that of betweenness when a large amount of noisy data is added to an interactome. Finally, we combine gene expression data with interaction data in C. elegans and construct an interactome network for muscle-specific genes. We find that genes that rank high in terms of information flow in the muscle interactome network but not in the entire network tend to play important roles in muscle function. This framework for studying tissue-specific networks by the information flow model can be applied to other tissues and other organisms as well. 2010-05-05T13:58:49Z 2010-05-05T13:58:49Z 2009-04 2008-09 Article http://purl.org/eprint/type/JournalArticle 1553-734X 1553-7358 http://hdl.handle.net/1721.1/54708 Missiuro, Patrycja Vasilyev et al. “Information Flow Analysis of Interactome Networks.” PLoS Comput Biol 5.4 (2009): e1000350. https://orcid.org/0000-0003-2432-4678 en_US http://dx.doi.org/10.1371/journal.pcbi.1000350 PLoS Computational Biology Creative Commons Attribution http://creativecommons.org/licenses/by/2.5/ application/pdf Public Library of Science PLoS
spellingShingle Liu, Kesheng
Ge, Hui
Ross, Brian Christopher
Missiuro, Patrycja Vasilyev
Zhao, Guoyan
Liu, Jun S.
Zou, Lihua
Information Flow Analysis of Interactome Networks
title Information Flow Analysis of Interactome Networks
title_full Information Flow Analysis of Interactome Networks
title_fullStr Information Flow Analysis of Interactome Networks
title_full_unstemmed Information Flow Analysis of Interactome Networks
title_short Information Flow Analysis of Interactome Networks
title_sort information flow analysis of interactome networks
url http://hdl.handle.net/1721.1/54708
https://orcid.org/0000-0003-2432-4678
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