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Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression

Yes-associated Protein (YAP) is a transcriptional co-activator that regulates cell proliferation and survival by binding to a select set of enhancers for target gene activation. How YAP coordinates these transcriptional responses is unknown. Here, we demonstrate that YAP forms liquid-like condensate...

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Autores principales: Cai, Danfeng, Feliciano, Daniel, Dong, Peng, Flores, Eduardo, Gruebele, Martin, Porat-Shliom, Natalie, Sukenik, Shahar, Liu, Zhe, Lippincott-Schwartz, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259329/
https://www.ncbi.nlm.nih.gov/pubmed/31792379
http://dx.doi.org/10.1038/s41556-019-0433-z
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author Cai, Danfeng
Feliciano, Daniel
Dong, Peng
Flores, Eduardo
Gruebele, Martin
Porat-Shliom, Natalie
Sukenik, Shahar
Liu, Zhe
Lippincott-Schwartz, Jennifer
author_facet Cai, Danfeng
Feliciano, Daniel
Dong, Peng
Flores, Eduardo
Gruebele, Martin
Porat-Shliom, Natalie
Sukenik, Shahar
Liu, Zhe
Lippincott-Schwartz, Jennifer
author_sort Cai, Danfeng
collection PubMed
description Yes-associated Protein (YAP) is a transcriptional co-activator that regulates cell proliferation and survival by binding to a select set of enhancers for target gene activation. How YAP coordinates these transcriptional responses is unknown. Here, we demonstrate that YAP forms liquid-like condensates in the nucleus. Formed within seconds of hyperosmotic stress, YAP condensates compartmentalized YAP’s transcription factor TEAD1 and other YAP-related co-activators, including TAZ, and subsequently induced transcription of YAP-specific proliferation genes. Super-resolution imaging using Assay for Transposase Accessible Chromatin with photoactivated localization microscopy (ATAC-PALM) revealed that YAP nuclear condensates were areas enriched in accessible chromatin domains organized as super-enhancers. Initially devoid of RNA Polymerase II (RNAPII), the accessible chromatin domains later acquired RNAPII, transcribing RNA. Removal of YAP’s intrinsically-disordered transcription activation domain (TAD) prevented YAP condensate formation and diminished downstream YAP signaling. Thus, dynamic changes in genome organization and gene activation during YAP reprogramming is mediated by liquid-liquid phase separation.
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spelling pubmed-82593292021-07-06 Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression Cai, Danfeng Feliciano, Daniel Dong, Peng Flores, Eduardo Gruebele, Martin Porat-Shliom, Natalie Sukenik, Shahar Liu, Zhe Lippincott-Schwartz, Jennifer Nat Cell Biol Article Yes-associated Protein (YAP) is a transcriptional co-activator that regulates cell proliferation and survival by binding to a select set of enhancers for target gene activation. How YAP coordinates these transcriptional responses is unknown. Here, we demonstrate that YAP forms liquid-like condensates in the nucleus. Formed within seconds of hyperosmotic stress, YAP condensates compartmentalized YAP’s transcription factor TEAD1 and other YAP-related co-activators, including TAZ, and subsequently induced transcription of YAP-specific proliferation genes. Super-resolution imaging using Assay for Transposase Accessible Chromatin with photoactivated localization microscopy (ATAC-PALM) revealed that YAP nuclear condensates were areas enriched in accessible chromatin domains organized as super-enhancers. Initially devoid of RNA Polymerase II (RNAPII), the accessible chromatin domains later acquired RNAPII, transcribing RNA. Removal of YAP’s intrinsically-disordered transcription activation domain (TAD) prevented YAP condensate formation and diminished downstream YAP signaling. Thus, dynamic changes in genome organization and gene activation during YAP reprogramming is mediated by liquid-liquid phase separation. 2019-12-02 2019-12 /pmc/articles/PMC8259329/ /pubmed/31792379 http://dx.doi.org/10.1038/s41556-019-0433-z Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Cai, Danfeng
Feliciano, Daniel
Dong, Peng
Flores, Eduardo
Gruebele, Martin
Porat-Shliom, Natalie
Sukenik, Shahar
Liu, Zhe
Lippincott-Schwartz, Jennifer
Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title_full Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title_fullStr Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title_full_unstemmed Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title_short Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
title_sort phase separation of yap reorganizes genome topology for long-term yap target gene expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259329/
https://www.ncbi.nlm.nih.gov/pubmed/31792379
http://dx.doi.org/10.1038/s41556-019-0433-z
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