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Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor

Notch signaling controls many developmental processes by regulating gene expression. Notch-dependent enhancers recruit activation complexes consisting of the Notch intracellular domain, the Cbf/Su(H)/Lag1 (CSL) transcription factor (TF), and the Mastermind co-factor via two types of DNA sites: monom...

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Autores principales: Kuang, Yi, Pyo, Anna, Eafergan, Natanel, Cain, Brittany, Gutzwiller, Lisa M., Axelrod, Ofri, Gagliani, Ellen K., Weirauch, Matthew T., Kopan, Raphael, Kovall, Rhett A., Sprinzak, David, Gebelein, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494340/
https://www.ncbi.nlm.nih.gov/pubmed/34559800
http://dx.doi.org/10.1371/journal.pgen.1009039
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author Kuang, Yi
Pyo, Anna
Eafergan, Natanel
Cain, Brittany
Gutzwiller, Lisa M.
Axelrod, Ofri
Gagliani, Ellen K.
Weirauch, Matthew T.
Kopan, Raphael
Kovall, Rhett A.
Sprinzak, David
Gebelein, Brian
author_facet Kuang, Yi
Pyo, Anna
Eafergan, Natanel
Cain, Brittany
Gutzwiller, Lisa M.
Axelrod, Ofri
Gagliani, Ellen K.
Weirauch, Matthew T.
Kopan, Raphael
Kovall, Rhett A.
Sprinzak, David
Gebelein, Brian
author_sort Kuang, Yi
collection PubMed
description Notch signaling controls many developmental processes by regulating gene expression. Notch-dependent enhancers recruit activation complexes consisting of the Notch intracellular domain, the Cbf/Su(H)/Lag1 (CSL) transcription factor (TF), and the Mastermind co-factor via two types of DNA sites: monomeric CSL sites and cooperative dimer sites called Su(H) paired sites (SPS). Intriguingly, the CSL TF can also bind co-repressors to negatively regulate transcription via these same sites. Here, we tested how synthetic enhancers with monomeric CSL sites versus dimeric SPSs bind Drosophila Su(H) complexes in vitro and mediate transcriptional outcomes in vivo. Our findings reveal that while the Su(H)/Hairless co-repressor complex similarly binds SPS and CSL sites in an additive manner, the Notch activation complex binds SPSs, but not CSL sites, in a cooperative manner. Moreover, transgenic reporters with SPSs mediate stronger, more consistent transcription and are more resistant to increased Hairless co-repressor expression compared to reporters with the same number of CSL sites. These findings support a model in which SPS containing enhancers preferentially recruit cooperative Notch activation complexes over Hairless repression complexes to ensure consistent target gene activation.
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spelling pubmed-84943402021-10-07 Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor Kuang, Yi Pyo, Anna Eafergan, Natanel Cain, Brittany Gutzwiller, Lisa M. Axelrod, Ofri Gagliani, Ellen K. Weirauch, Matthew T. Kopan, Raphael Kovall, Rhett A. Sprinzak, David Gebelein, Brian PLoS Genet Research Article Notch signaling controls many developmental processes by regulating gene expression. Notch-dependent enhancers recruit activation complexes consisting of the Notch intracellular domain, the Cbf/Su(H)/Lag1 (CSL) transcription factor (TF), and the Mastermind co-factor via two types of DNA sites: monomeric CSL sites and cooperative dimer sites called Su(H) paired sites (SPS). Intriguingly, the CSL TF can also bind co-repressors to negatively regulate transcription via these same sites. Here, we tested how synthetic enhancers with monomeric CSL sites versus dimeric SPSs bind Drosophila Su(H) complexes in vitro and mediate transcriptional outcomes in vivo. Our findings reveal that while the Su(H)/Hairless co-repressor complex similarly binds SPS and CSL sites in an additive manner, the Notch activation complex binds SPSs, but not CSL sites, in a cooperative manner. Moreover, transgenic reporters with SPSs mediate stronger, more consistent transcription and are more resistant to increased Hairless co-repressor expression compared to reporters with the same number of CSL sites. These findings support a model in which SPS containing enhancers preferentially recruit cooperative Notch activation complexes over Hairless repression complexes to ensure consistent target gene activation. Public Library of Science 2021-09-24 /pmc/articles/PMC8494340/ /pubmed/34559800 http://dx.doi.org/10.1371/journal.pgen.1009039 Text en © 2021 Kuang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kuang, Yi
Pyo, Anna
Eafergan, Natanel
Cain, Brittany
Gutzwiller, Lisa M.
Axelrod, Ofri
Gagliani, Ellen K.
Weirauch, Matthew T.
Kopan, Raphael
Kovall, Rhett A.
Sprinzak, David
Gebelein, Brian
Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title_full Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title_fullStr Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title_full_unstemmed Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title_short Enhancers with cooperative Notch binding sites are more resistant to regulation by the Hairless co-repressor
title_sort enhancers with cooperative notch binding sites are more resistant to regulation by the hairless co-repressor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494340/
https://www.ncbi.nlm.nih.gov/pubmed/34559800
http://dx.doi.org/10.1371/journal.pgen.1009039
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