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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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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. |
format | Online Article Text |
id | pubmed-8259329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
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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