Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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
_version_ 1783507315713900544
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
work_keys_str_mv AT hackettseanr learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT baltzedwarda learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT corammarc learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT wranikberndj learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT kimgriffin learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT bakeradam learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT fanminjie learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT hendricksondavidg learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT berndlmarc learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries
AT mcisaacrscott learningcausalnetworksusinginducibletranscriptionfactorsandtranscriptomewidetimeseries