Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ranea, Juan A. G., Morilla, Ian, Lees, Jon G., Reid, Adam J., Yeats, Corin, Clegg, Andrew B., Sanchez-Jimenez, Francisca, Orengo, Christine
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
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
_version_ 1782187128837373952
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
work_keys_str_mv AT raneajuanag findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT morillaian findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT leesjong findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT reidadamj findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT yeatscorin findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT cleggandrewb findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT sanchezjimenezfrancisca findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling
AT orengochristine findingthedarkmatterinhumanandyeastproteinnetworkpredictionandmodelling