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The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling

Hippo signaling controls cellular processes that ultimately impact organogenesis and homeostasis. Consequently, disease states including cancer can emerge when signaling is deregulated. The major pathway transducers Yap and Taz require cofactors to impart transcriptional control over target genes. R...

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Detalles Bibliográficos
Autores principales: Hillmer, Ryan E., Link, Brian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562424/
https://www.ncbi.nlm.nih.gov/pubmed/31137701
http://dx.doi.org/10.3390/cells8050502
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author Hillmer, Ryan E.
Link, Brian A.
author_facet Hillmer, Ryan E.
Link, Brian A.
author_sort Hillmer, Ryan E.
collection PubMed
description Hippo signaling controls cellular processes that ultimately impact organogenesis and homeostasis. Consequently, disease states including cancer can emerge when signaling is deregulated. The major pathway transducers Yap and Taz require cofactors to impart transcriptional control over target genes. Research into Yap/Taz-mediated epigenetic modifications has revealed their association with chromatin-remodeling complex proteins as a means of altering chromatin structure, therefore affecting accessibility and activity of target genes. Specifically, Yap/Taz have been found to associate with factors of the GAGA, Ncoa6, Mediator, Switch/sucrose nonfermentable (SWI/SNF), and Nucleosome Remodeling and Deacetylase (NuRD) chromatin-remodeling complexes to alter the accessibility of target genes. This review highlights the different mechanisms by which Yap/Taz collaborate with other factors to modify DNA packing at specific loci to either activate or repress target gene transcription.
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spelling pubmed-65624242019-06-17 The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling Hillmer, Ryan E. Link, Brian A. Cells Review Hippo signaling controls cellular processes that ultimately impact organogenesis and homeostasis. Consequently, disease states including cancer can emerge when signaling is deregulated. The major pathway transducers Yap and Taz require cofactors to impart transcriptional control over target genes. Research into Yap/Taz-mediated epigenetic modifications has revealed their association with chromatin-remodeling complex proteins as a means of altering chromatin structure, therefore affecting accessibility and activity of target genes. Specifically, Yap/Taz have been found to associate with factors of the GAGA, Ncoa6, Mediator, Switch/sucrose nonfermentable (SWI/SNF), and Nucleosome Remodeling and Deacetylase (NuRD) chromatin-remodeling complexes to alter the accessibility of target genes. This review highlights the different mechanisms by which Yap/Taz collaborate with other factors to modify DNA packing at specific loci to either activate or repress target gene transcription. MDPI 2019-05-24 /pmc/articles/PMC6562424/ /pubmed/31137701 http://dx.doi.org/10.3390/cells8050502 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hillmer, Ryan E.
Link, Brian A.
The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title_full The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title_fullStr The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title_full_unstemmed The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title_short The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
title_sort roles of hippo signaling transducers yap and taz in chromatin remodeling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562424/
https://www.ncbi.nlm.nih.gov/pubmed/31137701
http://dx.doi.org/10.3390/cells8050502
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