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The Architecture of the Human RNA-Binding Protein Regulatory Network

RNA-binding proteins (RBPs) are key players of post-transcriptional regulation of gene expression, relying on competitive and cooperative interactions to fine-tune their action. Several studies have described individual interactions of RBPs with RBP mRNAs. Here we present a systematic network invest...

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Detalles Bibliográficos
Autores principales: Quattrone, Alessandro, Dassi, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864347/
https://www.ncbi.nlm.nih.gov/pubmed/31733516
http://dx.doi.org/10.1016/j.isci.2019.10.058
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author Quattrone, Alessandro
Dassi, Erik
author_facet Quattrone, Alessandro
Dassi, Erik
author_sort Quattrone, Alessandro
collection PubMed
description RNA-binding proteins (RBPs) are key players of post-transcriptional regulation of gene expression, relying on competitive and cooperative interactions to fine-tune their action. Several studies have described individual interactions of RBPs with RBP mRNAs. Here we present a systematic network investigation of fifty thousand interactions between RBPs and the UTRs of RBP mRNAs. We identified two structural features in this network. RBP clusters are groups of densely interconnected RBPs co-binding their targets, suggesting a tight control of cooperative and competitive behaviors. RBP chains are hierarchical structures connecting RBP clusters and driven by evolutionarily ancient RBPs. These features suggest that RBP chains may coordinate the different cell programs controlled by RBP clusters. Under this model, the regulatory signal flows through chains from one cluster to another, implementing elaborate regulatory plans. This work thus suggests RBP-RBP interactions as a backbone driving post-transcriptional regulation of gene expression to control RBPs action on their targets.
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spelling pubmed-68643472019-11-22 The Architecture of the Human RNA-Binding Protein Regulatory Network Quattrone, Alessandro Dassi, Erik iScience Article RNA-binding proteins (RBPs) are key players of post-transcriptional regulation of gene expression, relying on competitive and cooperative interactions to fine-tune their action. Several studies have described individual interactions of RBPs with RBP mRNAs. Here we present a systematic network investigation of fifty thousand interactions between RBPs and the UTRs of RBP mRNAs. We identified two structural features in this network. RBP clusters are groups of densely interconnected RBPs co-binding their targets, suggesting a tight control of cooperative and competitive behaviors. RBP chains are hierarchical structures connecting RBP clusters and driven by evolutionarily ancient RBPs. These features suggest that RBP chains may coordinate the different cell programs controlled by RBP clusters. Under this model, the regulatory signal flows through chains from one cluster to another, implementing elaborate regulatory plans. This work thus suggests RBP-RBP interactions as a backbone driving post-transcriptional regulation of gene expression to control RBPs action on their targets. Elsevier 2019-11-01 /pmc/articles/PMC6864347/ /pubmed/31733516 http://dx.doi.org/10.1016/j.isci.2019.10.058 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Quattrone, Alessandro
Dassi, Erik
The Architecture of the Human RNA-Binding Protein Regulatory Network
title The Architecture of the Human RNA-Binding Protein Regulatory Network
title_full The Architecture of the Human RNA-Binding Protein Regulatory Network
title_fullStr The Architecture of the Human RNA-Binding Protein Regulatory Network
title_full_unstemmed The Architecture of the Human RNA-Binding Protein Regulatory Network
title_short The Architecture of the Human RNA-Binding Protein Regulatory Network
title_sort architecture of the human rna-binding protein regulatory network
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864347/
https://www.ncbi.nlm.nih.gov/pubmed/31733516
http://dx.doi.org/10.1016/j.isci.2019.10.058
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