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From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL

While gene expression profiling is commonly used to gain an overview of cellular processes, the identification of upstream processes that drive expression changes remains a challenge. To address this issue, we introduce CARNIVAL, a causal network contextualization tool which derives network architec...

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Autores principales: Liu, Anika, Trairatphisan, Panuwat, Gjerga, Enio, Didangelos, Athanasios, Barratt, Jonathan, Saez-Rodriguez, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848167/
https://www.ncbi.nlm.nih.gov/pubmed/31728204
http://dx.doi.org/10.1038/s41540-019-0118-z
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author Liu, Anika
Trairatphisan, Panuwat
Gjerga, Enio
Didangelos, Athanasios
Barratt, Jonathan
Saez-Rodriguez, Julio
author_facet Liu, Anika
Trairatphisan, Panuwat
Gjerga, Enio
Didangelos, Athanasios
Barratt, Jonathan
Saez-Rodriguez, Julio
author_sort Liu, Anika
collection PubMed
description While gene expression profiling is commonly used to gain an overview of cellular processes, the identification of upstream processes that drive expression changes remains a challenge. To address this issue, we introduce CARNIVAL, a causal network contextualization tool which derives network architectures from gene expression footprints. CARNIVAL (CAusal Reasoning pipeline for Network identification using Integer VALue programming) integrates different sources of prior knowledge including signed and directed protein–protein interactions, transcription factor targets, and pathway signatures. The use of prior knowledge in CARNIVAL enables capturing a broad set of upstream cellular processes and regulators, leading to a higher accuracy when benchmarked against related tools. Implementation as an integer linear programming (ILP) problem guarantees efficient computation. As a case study, we applied CARNIVAL to contextualize signaling networks from gene expression data in IgA nephropathy (IgAN), a condition that can lead to chronic kidney disease. CARNIVAL identified specific signaling pathways and associated mediators dysregulated in IgAN including Wnt and TGF-β, which we subsequently validated experimentally. These results demonstrated how CARNIVAL generates hypotheses on potential upstream alterations that propagate through signaling networks, providing insights into diseases.
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spelling pubmed-68481672019-11-14 From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL Liu, Anika Trairatphisan, Panuwat Gjerga, Enio Didangelos, Athanasios Barratt, Jonathan Saez-Rodriguez, Julio NPJ Syst Biol Appl Article While gene expression profiling is commonly used to gain an overview of cellular processes, the identification of upstream processes that drive expression changes remains a challenge. To address this issue, we introduce CARNIVAL, a causal network contextualization tool which derives network architectures from gene expression footprints. CARNIVAL (CAusal Reasoning pipeline for Network identification using Integer VALue programming) integrates different sources of prior knowledge including signed and directed protein–protein interactions, transcription factor targets, and pathway signatures. The use of prior knowledge in CARNIVAL enables capturing a broad set of upstream cellular processes and regulators, leading to a higher accuracy when benchmarked against related tools. Implementation as an integer linear programming (ILP) problem guarantees efficient computation. As a case study, we applied CARNIVAL to contextualize signaling networks from gene expression data in IgA nephropathy (IgAN), a condition that can lead to chronic kidney disease. CARNIVAL identified specific signaling pathways and associated mediators dysregulated in IgAN including Wnt and TGF-β, which we subsequently validated experimentally. These results demonstrated how CARNIVAL generates hypotheses on potential upstream alterations that propagate through signaling networks, providing insights into diseases. Nature Publishing Group UK 2019-11-11 /pmc/articles/PMC6848167/ /pubmed/31728204 http://dx.doi.org/10.1038/s41540-019-0118-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Anika
Trairatphisan, Panuwat
Gjerga, Enio
Didangelos, Athanasios
Barratt, Jonathan
Saez-Rodriguez, Julio
From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title_full From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title_fullStr From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title_full_unstemmed From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title_short From expression footprints to causal pathways: contextualizing large signaling networks with CARNIVAL
title_sort from expression footprints to causal pathways: contextualizing large signaling networks with carnival
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848167/
https://www.ncbi.nlm.nih.gov/pubmed/31728204
http://dx.doi.org/10.1038/s41540-019-0118-z
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