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Learning causal networks using inducible transcription factors and transcriptome‐wide time series
We present IDEA (the Induction Dynamics gene Expression Atlas), a dataset constructed by independently inducing hundreds of transcription factors (TFs) and measuring timecourses of the resulting gene expression responses in budding yeast. Each experiment captures a regulatory cascade connecting a si...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076914/ https://www.ncbi.nlm.nih.gov/pubmed/32181581 http://dx.doi.org/10.15252/msb.20199174 |
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author | Hackett, Sean R Baltz, Edward A Coram, Marc Wranik, Bernd J Kim, Griffin Baker, Adam Fan, Minjie Hendrickson, David G Berndl, Marc McIsaac, R Scott |
author_facet | Hackett, Sean R Baltz, Edward A Coram, Marc Wranik, Bernd J Kim, Griffin Baker, Adam Fan, Minjie Hendrickson, David G Berndl, Marc McIsaac, R Scott |
author_sort | Hackett, Sean R |
collection | PubMed |
description | We present IDEA (the Induction Dynamics gene Expression Atlas), a dataset constructed by independently inducing hundreds of transcription factors (TFs) and measuring timecourses of the resulting gene expression responses in budding yeast. Each experiment captures a regulatory cascade connecting a single induced regulator to the genes it causally regulates. We discuss the regulatory cascade of a single TF, Aft1, in detail; however, IDEA contains > 200 TF induction experiments with 20 million individual observations and 100,000 signal‐containing dynamic responses. As an application of IDEA, we integrate all timecourses into a whole‐cell transcriptional model, which is used to predict and validate multiple new and underappreciated transcriptional regulators. We also find that the magnitudes of coefficients in this model are predictive of genetic interaction profile similarities. In addition to being a resource for exploring regulatory connectivity between TFs and their target genes, our modeling approach shows that combining rapid perturbations of individual genes with genome‐scale time‐series measurements is an effective strategy for elucidating gene regulatory networks. |
format | Online Article Text |
id | pubmed-7076914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70769142020-03-19 Learning causal networks using inducible transcription factors and transcriptome‐wide time series Hackett, Sean R Baltz, Edward A Coram, Marc Wranik, Bernd J Kim, Griffin Baker, Adam Fan, Minjie Hendrickson, David G Berndl, Marc McIsaac, R Scott Mol Syst Biol Articles We present IDEA (the Induction Dynamics gene Expression Atlas), a dataset constructed by independently inducing hundreds of transcription factors (TFs) and measuring timecourses of the resulting gene expression responses in budding yeast. Each experiment captures a regulatory cascade connecting a single induced regulator to the genes it causally regulates. We discuss the regulatory cascade of a single TF, Aft1, in detail; however, IDEA contains > 200 TF induction experiments with 20 million individual observations and 100,000 signal‐containing dynamic responses. As an application of IDEA, we integrate all timecourses into a whole‐cell transcriptional model, which is used to predict and validate multiple new and underappreciated transcriptional regulators. We also find that the magnitudes of coefficients in this model are predictive of genetic interaction profile similarities. In addition to being a resource for exploring regulatory connectivity between TFs and their target genes, our modeling approach shows that combining rapid perturbations of individual genes with genome‐scale time‐series measurements is an effective strategy for elucidating gene regulatory networks. John Wiley and Sons Inc. 2020-03-17 /pmc/articles/PMC7076914/ /pubmed/32181581 http://dx.doi.org/10.15252/msb.20199174 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Hackett, Sean R Baltz, Edward A Coram, Marc Wranik, Bernd J Kim, Griffin Baker, Adam Fan, Minjie Hendrickson, David G Berndl, Marc McIsaac, R Scott Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title | Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title_full | Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title_fullStr | Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title_full_unstemmed | Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title_short | Learning causal networks using inducible transcription factors and transcriptome‐wide time series |
title_sort | learning causal networks using inducible transcription factors and transcriptome‐wide time series |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076914/ https://www.ncbi.nlm.nih.gov/pubmed/32181581 http://dx.doi.org/10.15252/msb.20199174 |
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