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Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling
Accurate modelling of biological systems requires a deeper and more complete knowledge about the molecular components and their functional associations than we currently have. Traditionally, new knowledge on protein associations generated by experiments has played a central role in systems modelling...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944794/ https://www.ncbi.nlm.nih.gov/pubmed/20885791 http://dx.doi.org/10.1371/journal.pcbi.1000945 |
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author | Ranea, Juan A. G. Morilla, Ian Lees, Jon G. Reid, Adam J. Yeats, Corin Clegg, Andrew B. Sanchez-Jimenez, Francisca Orengo, Christine |
author_facet | Ranea, Juan A. G. Morilla, Ian Lees, Jon G. Reid, Adam J. Yeats, Corin Clegg, Andrew B. Sanchez-Jimenez, Francisca Orengo, Christine |
author_sort | Ranea, Juan A. G. |
collection | PubMed |
description | Accurate modelling of biological systems requires a deeper and more complete knowledge about the molecular components and their functional associations than we currently have. Traditionally, new knowledge on protein associations generated by experiments has played a central role in systems modelling, in contrast to generally less trusted bio-computational predictions. However, we will not achieve realistic modelling of complex molecular systems if the current experimental designs lead to biased screenings of real protein networks and leave large, functionally important areas poorly characterised. To assess the likelihood of this, we have built comprehensive network models of the yeast and human proteomes by using a meta-statistical integration of diverse computationally predicted protein association datasets. We have compared these predicted networks against combined experimental datasets from seven biological resources at different level of statistical significance. These eukaryotic predicted networks resemble all the topological and noise features of the experimentally inferred networks in both species, and we also show that this observation is not due to random behaviour. In addition, the topology of the predicted networks contains information on true protein associations, beyond the constitutive first order binary predictions. We also observe that most of the reliable predicted protein associations are experimentally uncharacterised in our models, constituting the hidden or “dark matter” of networks by analogy to astronomical systems. Some of this dark matter shows enrichment of particular functions and contains key functional elements of protein networks, such as hubs associated with important functional areas like the regulation of Ras protein signal transduction in human cells. Thus, characterising this large and functionally important dark matter, elusive to established experimental designs, may be crucial for modelling biological systems. In any case, these predictions provide a valuable guide to these experimentally elusive regions. |
format | Text |
id | pubmed-2944794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29447942010-09-30 Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling Ranea, Juan A. G. Morilla, Ian Lees, Jon G. Reid, Adam J. Yeats, Corin Clegg, Andrew B. Sanchez-Jimenez, Francisca Orengo, Christine PLoS Comput Biol Research Article Accurate modelling of biological systems requires a deeper and more complete knowledge about the molecular components and their functional associations than we currently have. Traditionally, new knowledge on protein associations generated by experiments has played a central role in systems modelling, in contrast to generally less trusted bio-computational predictions. However, we will not achieve realistic modelling of complex molecular systems if the current experimental designs lead to biased screenings of real protein networks and leave large, functionally important areas poorly characterised. To assess the likelihood of this, we have built comprehensive network models of the yeast and human proteomes by using a meta-statistical integration of diverse computationally predicted protein association datasets. We have compared these predicted networks against combined experimental datasets from seven biological resources at different level of statistical significance. These eukaryotic predicted networks resemble all the topological and noise features of the experimentally inferred networks in both species, and we also show that this observation is not due to random behaviour. In addition, the topology of the predicted networks contains information on true protein associations, beyond the constitutive first order binary predictions. We also observe that most of the reliable predicted protein associations are experimentally uncharacterised in our models, constituting the hidden or “dark matter” of networks by analogy to astronomical systems. Some of this dark matter shows enrichment of particular functions and contains key functional elements of protein networks, such as hubs associated with important functional areas like the regulation of Ras protein signal transduction in human cells. Thus, characterising this large and functionally important dark matter, elusive to established experimental designs, may be crucial for modelling biological systems. In any case, these predictions provide a valuable guide to these experimentally elusive regions. Public Library of Science 2010-09-23 /pmc/articles/PMC2944794/ /pubmed/20885791 http://dx.doi.org/10.1371/journal.pcbi.1000945 Text en Ranea 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 Ranea, Juan A. G. Morilla, Ian Lees, Jon G. Reid, Adam J. Yeats, Corin Clegg, Andrew B. Sanchez-Jimenez, Francisca Orengo, Christine Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title | Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title_full | Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title_fullStr | Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title_full_unstemmed | Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title_short | Finding the “Dark Matter” in Human and Yeast Protein Network Prediction and Modelling |
title_sort | finding the “dark matter” in human and yeast protein network prediction and modelling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944794/ https://www.ncbi.nlm.nih.gov/pubmed/20885791 http://dx.doi.org/10.1371/journal.pcbi.1000945 |
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