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Protein Interaction Networks—More Than Mere Modules

It is widely believed that the modular organization of cellular function is reflected in a modular structure of molecular networks. A common view is that a “module” in a network is a cohesively linked group of nodes, densely connected internally and sparsely interacting with the rest of the network....

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Detalles Bibliográficos
Autores principales: Pinkert, Stefan, Schultz, Jörg, Reichardt, Jörg
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813263/
https://www.ncbi.nlm.nih.gov/pubmed/20126533
http://dx.doi.org/10.1371/journal.pcbi.1000659
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author Pinkert, Stefan
Schultz, Jörg
Reichardt, Jörg
author_facet Pinkert, Stefan
Schultz, Jörg
Reichardt, Jörg
author_sort Pinkert, Stefan
collection PubMed
description It is widely believed that the modular organization of cellular function is reflected in a modular structure of molecular networks. A common view is that a “module” in a network is a cohesively linked group of nodes, densely connected internally and sparsely interacting with the rest of the network. Many algorithms try to identify functional modules in protein-interaction networks (PIN) by searching for such cohesive groups of proteins. Here, we present an alternative approach independent of any prior definition of what actually constitutes a “module”. In a self-consistent manner, proteins are grouped into “functional roles” if they interact in similar ways with other proteins according to their functional roles. Such grouping may well result in cohesive modules again, but only if the network structure actually supports this. We applied our method to the PIN from the Human Protein Reference Database (HPRD) and found that a representation of the network in terms of cohesive modules, at least on a global scale, does not optimally represent the network's structure because it focuses on finding independent groups of proteins. In contrast, a decomposition into functional roles is able to depict the structure much better as it also takes into account the interdependencies between roles and even allows groupings based on the absence of interactions between proteins in the same functional role. This, for example, is the case for transmembrane proteins, which could never be recognized as a cohesive group of nodes in a PIN. When mapping experimental methods onto the groups, we identified profound differences in the coverage suggesting that our method is able to capture experimental bias in the data, too. For example yeast-two-hybrid data were highly overrepresented in one particular group. Thus, there is more structure in protein-interaction networks than cohesive modules alone and we believe this finding can significantly improve automated function prediction algorithms.
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spelling pubmed-28132632010-02-03 Protein Interaction Networks—More Than Mere Modules Pinkert, Stefan Schultz, Jörg Reichardt, Jörg PLoS Comput Biol Research Article It is widely believed that the modular organization of cellular function is reflected in a modular structure of molecular networks. A common view is that a “module” in a network is a cohesively linked group of nodes, densely connected internally and sparsely interacting with the rest of the network. Many algorithms try to identify functional modules in protein-interaction networks (PIN) by searching for such cohesive groups of proteins. Here, we present an alternative approach independent of any prior definition of what actually constitutes a “module”. In a self-consistent manner, proteins are grouped into “functional roles” if they interact in similar ways with other proteins according to their functional roles. Such grouping may well result in cohesive modules again, but only if the network structure actually supports this. We applied our method to the PIN from the Human Protein Reference Database (HPRD) and found that a representation of the network in terms of cohesive modules, at least on a global scale, does not optimally represent the network's structure because it focuses on finding independent groups of proteins. In contrast, a decomposition into functional roles is able to depict the structure much better as it also takes into account the interdependencies between roles and even allows groupings based on the absence of interactions between proteins in the same functional role. This, for example, is the case for transmembrane proteins, which could never be recognized as a cohesive group of nodes in a PIN. When mapping experimental methods onto the groups, we identified profound differences in the coverage suggesting that our method is able to capture experimental bias in the data, too. For example yeast-two-hybrid data were highly overrepresented in one particular group. Thus, there is more structure in protein-interaction networks than cohesive modules alone and we believe this finding can significantly improve automated function prediction algorithms. Public Library of Science 2010-01-29 /pmc/articles/PMC2813263/ /pubmed/20126533 http://dx.doi.org/10.1371/journal.pcbi.1000659 Text en Pinkert et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pinkert, Stefan
Schultz, Jörg
Reichardt, Jörg
Protein Interaction Networks—More Than Mere Modules
title Protein Interaction Networks—More Than Mere Modules
title_full Protein Interaction Networks—More Than Mere Modules
title_fullStr Protein Interaction Networks—More Than Mere Modules
title_full_unstemmed Protein Interaction Networks—More Than Mere Modules
title_short Protein Interaction Networks—More Than Mere Modules
title_sort protein interaction networks—more than mere modules
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813263/
https://www.ncbi.nlm.nih.gov/pubmed/20126533
http://dx.doi.org/10.1371/journal.pcbi.1000659
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