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Illuminating Dark Proteins using Reactome Pathways

Limited knowledge about a substantial portion of protein coding genes, known as “dark” proteins, hinders our understanding of their functions and potential therapeutic applications. To address this, we leveraged Reactome, the most comprehensive, open source, open-access pathway knowledgebase, to con...

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Autores principales: Brunson, Timothy, Sanati, Nasim, Matthews, Lisa, Haw, Robin, Beavers, Deidre, Shorser, Solomon, Sevilla, Cristoffer, Viteri, Guilherme, Conley, Patrick, Rothfels, Karen, Hermjakob, Henning, Stein, Lincoln, D’Eustachio, Peter, Wu, Guanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274615/
https://www.ncbi.nlm.nih.gov/pubmed/37333417
http://dx.doi.org/10.1101/2023.06.05.543335
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author Brunson, Timothy
Sanati, Nasim
Matthews, Lisa
Haw, Robin
Beavers, Deidre
Shorser, Solomon
Sevilla, Cristoffer
Viteri, Guilherme
Conley, Patrick
Rothfels, Karen
Hermjakob, Henning
Stein, Lincoln
D’Eustachio, Peter
Wu, Guanming
author_facet Brunson, Timothy
Sanati, Nasim
Matthews, Lisa
Haw, Robin
Beavers, Deidre
Shorser, Solomon
Sevilla, Cristoffer
Viteri, Guilherme
Conley, Patrick
Rothfels, Karen
Hermjakob, Henning
Stein, Lincoln
D’Eustachio, Peter
Wu, Guanming
author_sort Brunson, Timothy
collection PubMed
description Limited knowledge about a substantial portion of protein coding genes, known as “dark” proteins, hinders our understanding of their functions and potential therapeutic applications. To address this, we leveraged Reactome, the most comprehensive, open source, open-access pathway knowledgebase, to contextualize dark proteins within biological pathways. By integrating multiple resources and employing a random forest classifier trained on 106 protein/gene pairwise features, we predicted functional interactions between dark proteins and Reactome-annotated proteins. We then developed three scores to measure the interactions between dark proteins and Reactome pathways, utilizing enrichment analysis and fuzzy logic simulations. Correlation analysis of these scores with an independent single-cell RNA sequencing dataset provided supporting evidence for this approach. Furthermore, systematic natural language processing (NLP) analysis of over 22 million PubMed abstracts and manual checking of the literature associated with 20 randomly selected dark proteins reinforced the predicted interactions between proteins and pathways. To enhance the visualization and exploration of dark proteins within Reactome pathways, we developed the Reactome IDG portal, deployed at https://idg.reactome.org, a web application featuring tissue-specific protein and gene expression overlay, as well as drug interactions. Our integrated computational approach, together with the user-friendly web platform, offers a valuable resource for uncovering potential biological functions and therapeutic implications of dark proteins.
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spelling pubmed-102746152023-06-17 Illuminating Dark Proteins using Reactome Pathways Brunson, Timothy Sanati, Nasim Matthews, Lisa Haw, Robin Beavers, Deidre Shorser, Solomon Sevilla, Cristoffer Viteri, Guilherme Conley, Patrick Rothfels, Karen Hermjakob, Henning Stein, Lincoln D’Eustachio, Peter Wu, Guanming bioRxiv Article Limited knowledge about a substantial portion of protein coding genes, known as “dark” proteins, hinders our understanding of their functions and potential therapeutic applications. To address this, we leveraged Reactome, the most comprehensive, open source, open-access pathway knowledgebase, to contextualize dark proteins within biological pathways. By integrating multiple resources and employing a random forest classifier trained on 106 protein/gene pairwise features, we predicted functional interactions between dark proteins and Reactome-annotated proteins. We then developed three scores to measure the interactions between dark proteins and Reactome pathways, utilizing enrichment analysis and fuzzy logic simulations. Correlation analysis of these scores with an independent single-cell RNA sequencing dataset provided supporting evidence for this approach. Furthermore, systematic natural language processing (NLP) analysis of over 22 million PubMed abstracts and manual checking of the literature associated with 20 randomly selected dark proteins reinforced the predicted interactions between proteins and pathways. To enhance the visualization and exploration of dark proteins within Reactome pathways, we developed the Reactome IDG portal, deployed at https://idg.reactome.org, a web application featuring tissue-specific protein and gene expression overlay, as well as drug interactions. Our integrated computational approach, together with the user-friendly web platform, offers a valuable resource for uncovering potential biological functions and therapeutic implications of dark proteins. Cold Spring Harbor Laboratory 2023-06-05 /pmc/articles/PMC10274615/ /pubmed/37333417 http://dx.doi.org/10.1101/2023.06.05.543335 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Brunson, Timothy
Sanati, Nasim
Matthews, Lisa
Haw, Robin
Beavers, Deidre
Shorser, Solomon
Sevilla, Cristoffer
Viteri, Guilherme
Conley, Patrick
Rothfels, Karen
Hermjakob, Henning
Stein, Lincoln
D’Eustachio, Peter
Wu, Guanming
Illuminating Dark Proteins using Reactome Pathways
title Illuminating Dark Proteins using Reactome Pathways
title_full Illuminating Dark Proteins using Reactome Pathways
title_fullStr Illuminating Dark Proteins using Reactome Pathways
title_full_unstemmed Illuminating Dark Proteins using Reactome Pathways
title_short Illuminating Dark Proteins using Reactome Pathways
title_sort illuminating dark proteins using reactome pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274615/
https://www.ncbi.nlm.nih.gov/pubmed/37333417
http://dx.doi.org/10.1101/2023.06.05.543335
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