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Chemogenetic Minitool for Dissecting the Roles of Protein Phase Separation
[Image: see text] Biomolecular condensate is an emerging structural entity that regulates various cellular processes. Recent studies have discovered the phase-separation (PS) capability of several transcription factors (TFs) including YAP/TAZ upon biological stimuli, which provide new mechanisms of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375881/ https://www.ncbi.nlm.nih.gov/pubmed/37521779 http://dx.doi.org/10.1021/acscentsci.3c00251 |
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author | Chung, Chan-I Yang, Junjiao Shu, Xiaokun |
author_facet | Chung, Chan-I Yang, Junjiao Shu, Xiaokun |
author_sort | Chung, Chan-I |
collection | PubMed |
description | [Image: see text] Biomolecular condensate is an emerging structural entity that regulates various cellular processes. Recent studies have discovered the phase-separation (PS) capability of several transcription factors (TFs) including YAP/TAZ upon biological stimuli, which provide new mechanisms of gene regulation. However, it remains mostly unanswered as to whether PS from a diffuse state to a phase-separated state promotes gene transcription. To address this question, we have designed a chemogenetic tool, dubbed SPARK-ON, which manipulates the PS of YAP and TAZ without a biological stimulus, forming condensates that are transcriptionally active, containing the DNA-binding partner TEAD, genomic DNA, transcriptional machinery, and nascent RNA. Most importantly, PS of TAZ increases the transcription of its target genes. Therefore, our data indicate that PS promotes gene transcription of TAZ. SPARK-ON is advantageous to current mutagenesis-based approaches that are often problematic when mutagenesis affects the transcriptional activity of a TF. Furthermore, protein abundance levels also affect gene transcription, but PS depends on protein abundance because PS occurs only when the protein level is above a saturation concentration. SPARK-ON decouples PS from protein abundance levels without introducing mutations and thus will find important applications in understanding the biological roles of PS for many TFs and other biomolecular condensates. |
format | Online Article Text |
id | pubmed-10375881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103758812023-07-29 Chemogenetic Minitool for Dissecting the Roles of Protein Phase Separation Chung, Chan-I Yang, Junjiao Shu, Xiaokun ACS Cent Sci [Image: see text] Biomolecular condensate is an emerging structural entity that regulates various cellular processes. Recent studies have discovered the phase-separation (PS) capability of several transcription factors (TFs) including YAP/TAZ upon biological stimuli, which provide new mechanisms of gene regulation. However, it remains mostly unanswered as to whether PS from a diffuse state to a phase-separated state promotes gene transcription. To address this question, we have designed a chemogenetic tool, dubbed SPARK-ON, which manipulates the PS of YAP and TAZ without a biological stimulus, forming condensates that are transcriptionally active, containing the DNA-binding partner TEAD, genomic DNA, transcriptional machinery, and nascent RNA. Most importantly, PS of TAZ increases the transcription of its target genes. Therefore, our data indicate that PS promotes gene transcription of TAZ. SPARK-ON is advantageous to current mutagenesis-based approaches that are often problematic when mutagenesis affects the transcriptional activity of a TF. Furthermore, protein abundance levels also affect gene transcription, but PS depends on protein abundance because PS occurs only when the protein level is above a saturation concentration. SPARK-ON decouples PS from protein abundance levels without introducing mutations and thus will find important applications in understanding the biological roles of PS for many TFs and other biomolecular condensates. American Chemical Society 2023-07-07 /pmc/articles/PMC10375881/ /pubmed/37521779 http://dx.doi.org/10.1021/acscentsci.3c00251 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Chung, Chan-I Yang, Junjiao Shu, Xiaokun Chemogenetic Minitool for Dissecting the Roles of Protein Phase Separation |
title | Chemogenetic
Minitool for Dissecting the Roles of
Protein Phase Separation |
title_full | Chemogenetic
Minitool for Dissecting the Roles of
Protein Phase Separation |
title_fullStr | Chemogenetic
Minitool for Dissecting the Roles of
Protein Phase Separation |
title_full_unstemmed | Chemogenetic
Minitool for Dissecting the Roles of
Protein Phase Separation |
title_short | Chemogenetic
Minitool for Dissecting the Roles of
Protein Phase Separation |
title_sort | chemogenetic
minitool for dissecting the roles of
protein phase separation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375881/ https://www.ncbi.nlm.nih.gov/pubmed/37521779 http://dx.doi.org/10.1021/acscentsci.3c00251 |
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