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Dynamic regulatory module networks for inference of cell type–specific transcriptional networks

Changes in transcriptional regulatory networks can significantly alter cell fate. To gain insight into transcriptional dynamics, several studies have profiled bulk multi-omic data sets with parallel transcriptomic and epigenomic measurements at different stages of a developmental process. However, i...

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Autores principales: Siahpirani, Alireza Fotuhi, Knaack, Sara, Chasman, Deborah, Seirup, Morten, Sridharan, Rupa, Stewart, Ron, Thomson, James, Roy, Sushmita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9341506/
https://www.ncbi.nlm.nih.gov/pubmed/35705328
http://dx.doi.org/10.1101/gr.276542.121
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author Siahpirani, Alireza Fotuhi
Knaack, Sara
Chasman, Deborah
Seirup, Morten
Sridharan, Rupa
Stewart, Ron
Thomson, James
Roy, Sushmita
author_facet Siahpirani, Alireza Fotuhi
Knaack, Sara
Chasman, Deborah
Seirup, Morten
Sridharan, Rupa
Stewart, Ron
Thomson, James
Roy, Sushmita
author_sort Siahpirani, Alireza Fotuhi
collection PubMed
description Changes in transcriptional regulatory networks can significantly alter cell fate. To gain insight into transcriptional dynamics, several studies have profiled bulk multi-omic data sets with parallel transcriptomic and epigenomic measurements at different stages of a developmental process. However, integrating these data to infer cell type–specific regulatory networks is a major challenge. We present dynamic regulatory module networks (DRMNs), a novel approach to infer cell type–specific cis-regulatory networks and their dynamics. DRMN integrates expression, chromatin state, and accessibility to predict cis-regulators of context-specific expression, where context can be cell type, developmental stage, or time point, and uses multitask learning to capture network dynamics across linearly and hierarchically related contexts. We applied DRMNs to study regulatory network dynamics in three developmental processes, each showing different temporal relationships and measuring a different combination of regulatory genomic data sets: cellular reprogramming, liver dedifferentiation, and forward differentiation. DRMN identified known and novel regulators driving cell type–specific expression patterns, showing its broad applicability to examine dynamics of gene regulatory networks from linearly and hierarchically related multi-omic data sets.
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spelling pubmed-93415062022-08-16 Dynamic regulatory module networks for inference of cell type–specific transcriptional networks Siahpirani, Alireza Fotuhi Knaack, Sara Chasman, Deborah Seirup, Morten Sridharan, Rupa Stewart, Ron Thomson, James Roy, Sushmita Genome Res Method Changes in transcriptional regulatory networks can significantly alter cell fate. To gain insight into transcriptional dynamics, several studies have profiled bulk multi-omic data sets with parallel transcriptomic and epigenomic measurements at different stages of a developmental process. However, integrating these data to infer cell type–specific regulatory networks is a major challenge. We present dynamic regulatory module networks (DRMNs), a novel approach to infer cell type–specific cis-regulatory networks and their dynamics. DRMN integrates expression, chromatin state, and accessibility to predict cis-regulators of context-specific expression, where context can be cell type, developmental stage, or time point, and uses multitask learning to capture network dynamics across linearly and hierarchically related contexts. We applied DRMNs to study regulatory network dynamics in three developmental processes, each showing different temporal relationships and measuring a different combination of regulatory genomic data sets: cellular reprogramming, liver dedifferentiation, and forward differentiation. DRMN identified known and novel regulators driving cell type–specific expression patterns, showing its broad applicability to examine dynamics of gene regulatory networks from linearly and hierarchically related multi-omic data sets. Cold Spring Harbor Laboratory Press 2022-07 /pmc/articles/PMC9341506/ /pubmed/35705328 http://dx.doi.org/10.1101/gr.276542.121 Text en © 2022 Fotuhi Siahpirani et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Method
Siahpirani, Alireza Fotuhi
Knaack, Sara
Chasman, Deborah
Seirup, Morten
Sridharan, Rupa
Stewart, Ron
Thomson, James
Roy, Sushmita
Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title_full Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title_fullStr Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title_full_unstemmed Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title_short Dynamic regulatory module networks for inference of cell type–specific transcriptional networks
title_sort dynamic regulatory module networks for inference of cell type–specific transcriptional networks
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9341506/
https://www.ncbi.nlm.nih.gov/pubmed/35705328
http://dx.doi.org/10.1101/gr.276542.121
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