Reduced chromatin accessibility correlates with resistance to Notch activation

Notch signalling plays a key role in cell fate transitions, but how Notch activates distinct regulatory networks in closely related cell types is not well understood. Here the authors profile Notch and RBPJ targets in the developing mouse cortex and reveal how transcription factor occupancy and chro...

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Main Authors: Jelle van den Ameele, Robert Krautz, Seth W. Cheetham, Alex P. A. Donovan, Oriol Llorà-Batlle, Rebecca Yakob, Andrea H. Brand
Format: Article
Language:English
Published: Nature Portfolio 2022-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-29834-z
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author Jelle van den Ameele
Robert Krautz
Seth W. Cheetham
Alex P. A. Donovan
Oriol Llorà-Batlle
Rebecca Yakob
Andrea H. Brand
author_facet Jelle van den Ameele
Robert Krautz
Seth W. Cheetham
Alex P. A. Donovan
Oriol Llorà-Batlle
Rebecca Yakob
Andrea H. Brand
author_sort Jelle van den Ameele
collection DOAJ
description Notch signalling plays a key role in cell fate transitions, but how Notch activates distinct regulatory networks in closely related cell types is not well understood. Here the authors profile Notch and RBPJ targets in the developing mouse cortex and reveal how transcription factor occupancy and chromatin remodelling interact to direct differential gene expression during differentiation.
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spelling doaj.art-93dff00102e946c68df70fd26447e0de2022-12-22T03:03:49ZengNature PortfolioNature Communications2041-17232022-04-0113111010.1038/s41467-022-29834-zReduced chromatin accessibility correlates with resistance to Notch activationJelle van den Ameele0Robert Krautz1Seth W. Cheetham2Alex P. A. Donovan3Oriol Llorà-Batlle4Rebecca Yakob5Andrea H. Brand6The Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeThe Gurdon Institute and Department of Physiology, Development and Neuroscience, University of CambridgeNotch signalling plays a key role in cell fate transitions, but how Notch activates distinct regulatory networks in closely related cell types is not well understood. Here the authors profile Notch and RBPJ targets in the developing mouse cortex and reveal how transcription factor occupancy and chromatin remodelling interact to direct differential gene expression during differentiation.https://doi.org/10.1038/s41467-022-29834-z
spellingShingle Jelle van den Ameele
Robert Krautz
Seth W. Cheetham
Alex P. A. Donovan
Oriol Llorà-Batlle
Rebecca Yakob
Andrea H. Brand
Reduced chromatin accessibility correlates with resistance to Notch activation
Nature Communications
title Reduced chromatin accessibility correlates with resistance to Notch activation
title_full Reduced chromatin accessibility correlates with resistance to Notch activation
title_fullStr Reduced chromatin accessibility correlates with resistance to Notch activation
title_full_unstemmed Reduced chromatin accessibility correlates with resistance to Notch activation
title_short Reduced chromatin accessibility correlates with resistance to Notch activation
title_sort reduced chromatin accessibility correlates with resistance to notch activation
url https://doi.org/10.1038/s41467-022-29834-z
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