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On predicting regulatory genes by analysis of functional networks in C. elegans

BACKGROUND: Connectivity networks, which reflect multiple interactions between genes and proteins, possess not only a descriptive but also a predictive value, as new connections can be extrapolated and tested by means of computational analysis. Integration of different types of connectivity data (su...

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Autores principales: Valba, Olga V., Nechaev, Sergei K., Sterken, Mark G., Snoek, L. Basten, Kammenga, Jan E., Vasieva, Olga O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631084/
https://www.ncbi.nlm.nih.gov/pubmed/26535058
http://dx.doi.org/10.1186/s13040-015-0066-0
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author Valba, Olga V.
Nechaev, Sergei K.
Sterken, Mark G.
Snoek, L. Basten
Kammenga, Jan E.
Vasieva, Olga O.
author_facet Valba, Olga V.
Nechaev, Sergei K.
Sterken, Mark G.
Snoek, L. Basten
Kammenga, Jan E.
Vasieva, Olga O.
author_sort Valba, Olga V.
collection PubMed
description BACKGROUND: Connectivity networks, which reflect multiple interactions between genes and proteins, possess not only a descriptive but also a predictive value, as new connections can be extrapolated and tested by means of computational analysis. Integration of different types of connectivity data (such as co-expression and genetic interactions) in one network has proven to benefit ‘guilt by association’ analysis. However predictive values of connectives of different types, that had their specific functional meaning and topological characteristics were not obvious, and have been addressed in this analysis. METHODS: eQTL data for 3 experimental C.elegans age groups were retrieved from WormQTL. WormNet has been used to obtain pair-wise gene interactions. The Shortest Path Function (SPF) has been adopted for statistical validation of the co-expressed gene clusters and for computational prediction of their potential gene expression regulators from a network context. A new SPF-based algorithm has been applied to genetic interactions sub-networks adjacent to the clusters of co-expressed genes for ranking the most likely gene expression regulators causal to eQTLs. RESULTS: We have demonstrated that known co-expression and genetic interactions between C. elegans genes can be complementary in predicting gene expression regulators. Several algorithms were compared in respect to their predictive potential in different network connectivity contexts. We found that genes associated with eQTLs are highly clustered in a C. elegans co-expression sub-network, and their adjacent genetic interactions provide the optimal functional connectivity environment for application of the new SPF-based algorithm. It was successfully tested in the reverse-prediction analysis on groups of genes with known regulators and applied to co-expressed genes and experimentally observed expression quantitative trait loci (eQTLs). CONCLUSIONS: This analysis demonstrates differences in topology and connectivity of co-expression and genetic interactions sub-networks in WormNet. The modularity of less continuous genetic interaction network does not correspond to modularity of the dense network comprised by gene co-expression interactions. However the genetic interaction network can be used much more efficiently with the SPF method in prediction of potential regulators of gene expression. The developed method can be used for validation of functional significance of suggested eQTLs and a discovery of new regulatory modules.
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spelling pubmed-46310842015-11-04 On predicting regulatory genes by analysis of functional networks in C. elegans Valba, Olga V. Nechaev, Sergei K. Sterken, Mark G. Snoek, L. Basten Kammenga, Jan E. Vasieva, Olga O. BioData Min Research BACKGROUND: Connectivity networks, which reflect multiple interactions between genes and proteins, possess not only a descriptive but also a predictive value, as new connections can be extrapolated and tested by means of computational analysis. Integration of different types of connectivity data (such as co-expression and genetic interactions) in one network has proven to benefit ‘guilt by association’ analysis. However predictive values of connectives of different types, that had their specific functional meaning and topological characteristics were not obvious, and have been addressed in this analysis. METHODS: eQTL data for 3 experimental C.elegans age groups were retrieved from WormQTL. WormNet has been used to obtain pair-wise gene interactions. The Shortest Path Function (SPF) has been adopted for statistical validation of the co-expressed gene clusters and for computational prediction of their potential gene expression regulators from a network context. A new SPF-based algorithm has been applied to genetic interactions sub-networks adjacent to the clusters of co-expressed genes for ranking the most likely gene expression regulators causal to eQTLs. RESULTS: We have demonstrated that known co-expression and genetic interactions between C. elegans genes can be complementary in predicting gene expression regulators. Several algorithms were compared in respect to their predictive potential in different network connectivity contexts. We found that genes associated with eQTLs are highly clustered in a C. elegans co-expression sub-network, and their adjacent genetic interactions provide the optimal functional connectivity environment for application of the new SPF-based algorithm. It was successfully tested in the reverse-prediction analysis on groups of genes with known regulators and applied to co-expressed genes and experimentally observed expression quantitative trait loci (eQTLs). CONCLUSIONS: This analysis demonstrates differences in topology and connectivity of co-expression and genetic interactions sub-networks in WormNet. The modularity of less continuous genetic interaction network does not correspond to modularity of the dense network comprised by gene co-expression interactions. However the genetic interaction network can be used much more efficiently with the SPF method in prediction of potential regulators of gene expression. The developed method can be used for validation of functional significance of suggested eQTLs and a discovery of new regulatory modules. BioMed Central 2015-11-02 /pmc/articles/PMC4631084/ /pubmed/26535058 http://dx.doi.org/10.1186/s13040-015-0066-0 Text en © Valba et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Valba, Olga V.
Nechaev, Sergei K.
Sterken, Mark G.
Snoek, L. Basten
Kammenga, Jan E.
Vasieva, Olga O.
On predicting regulatory genes by analysis of functional networks in C. elegans
title On predicting regulatory genes by analysis of functional networks in C. elegans
title_full On predicting regulatory genes by analysis of functional networks in C. elegans
title_fullStr On predicting regulatory genes by analysis of functional networks in C. elegans
title_full_unstemmed On predicting regulatory genes by analysis of functional networks in C. elegans
title_short On predicting regulatory genes by analysis of functional networks in C. elegans
title_sort on predicting regulatory genes by analysis of functional networks in c. elegans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4631084/
https://www.ncbi.nlm.nih.gov/pubmed/26535058
http://dx.doi.org/10.1186/s13040-015-0066-0
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