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Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks

Regulatory networks that control gene expression are important in diverse biological contexts including stress response and development. Each gene's regulatory program is determined by module-level regulation (e.g. co-regulation via the same signaling system), as well as gene-specific determina...

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Autores principales: Roy, Sushmita, Lagree, Stephen, Hou, Zhonggang, Thomson, James A., Stewart, Ron, Gasch, Audrey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798279/
https://www.ncbi.nlm.nih.gov/pubmed/24146602
http://dx.doi.org/10.1371/journal.pcbi.1003252
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author Roy, Sushmita
Lagree, Stephen
Hou, Zhonggang
Thomson, James A.
Stewart, Ron
Gasch, Audrey P.
author_facet Roy, Sushmita
Lagree, Stephen
Hou, Zhonggang
Thomson, James A.
Stewart, Ron
Gasch, Audrey P.
author_sort Roy, Sushmita
collection PubMed
description Regulatory networks that control gene expression are important in diverse biological contexts including stress response and development. Each gene's regulatory program is determined by module-level regulation (e.g. co-regulation via the same signaling system), as well as gene-specific determinants that can fine-tune expression. We present a novel approach, Modular regulatory network learning with per gene information (MERLIN), that infers regulatory programs for individual genes while probabilistically constraining these programs to reveal module-level organization of regulatory networks. Using edge-, regulator- and module-based comparisons of simulated networks of known ground truth, we find MERLIN reconstructs regulatory programs of individual genes as well or better than existing approaches of network reconstruction, while additionally identifying modular organization of the regulatory networks. We use MERLIN to dissect global transcriptional behavior in two biological contexts: yeast stress response and human embryonic stem cell differentiation. Regulatory modules inferred by MERLIN capture co-regulatory relationships between signaling proteins and downstream transcription factors thereby revealing the upstream signaling systems controlling transcriptional responses. The inferred networks are enriched for regulators with genetic or physical interactions, supporting the inference, and identify modules of functionally related genes bound by the same transcriptional regulators. Our method combines the strengths of per-gene and per-module methods to reveal new insights into transcriptional regulation in stress and development.
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spelling pubmed-37982792013-10-21 Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks Roy, Sushmita Lagree, Stephen Hou, Zhonggang Thomson, James A. Stewart, Ron Gasch, Audrey P. PLoS Comput Biol Research Article Regulatory networks that control gene expression are important in diverse biological contexts including stress response and development. Each gene's regulatory program is determined by module-level regulation (e.g. co-regulation via the same signaling system), as well as gene-specific determinants that can fine-tune expression. We present a novel approach, Modular regulatory network learning with per gene information (MERLIN), that infers regulatory programs for individual genes while probabilistically constraining these programs to reveal module-level organization of regulatory networks. Using edge-, regulator- and module-based comparisons of simulated networks of known ground truth, we find MERLIN reconstructs regulatory programs of individual genes as well or better than existing approaches of network reconstruction, while additionally identifying modular organization of the regulatory networks. We use MERLIN to dissect global transcriptional behavior in two biological contexts: yeast stress response and human embryonic stem cell differentiation. Regulatory modules inferred by MERLIN capture co-regulatory relationships between signaling proteins and downstream transcription factors thereby revealing the upstream signaling systems controlling transcriptional responses. The inferred networks are enriched for regulators with genetic or physical interactions, supporting the inference, and identify modules of functionally related genes bound by the same transcriptional regulators. Our method combines the strengths of per-gene and per-module methods to reveal new insights into transcriptional regulation in stress and development. Public Library of Science 2013-10-17 /pmc/articles/PMC3798279/ /pubmed/24146602 http://dx.doi.org/10.1371/journal.pcbi.1003252 Text en © 2013 Roy 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
Roy, Sushmita
Lagree, Stephen
Hou, Zhonggang
Thomson, James A.
Stewart, Ron
Gasch, Audrey P.
Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title_full Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title_fullStr Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title_full_unstemmed Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title_short Integrated Module and Gene-Specific Regulatory Inference Implicates Upstream Signaling Networks
title_sort integrated module and gene-specific regulatory inference implicates upstream signaling networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798279/
https://www.ncbi.nlm.nih.gov/pubmed/24146602
http://dx.doi.org/10.1371/journal.pcbi.1003252
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