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Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging

Compartmentalization by liquid-liquid phase separation is implicated in transcription. It remains unclear whether and how transcriptional condensates accelerate the search of transcriptional regulatory factors for their target sites. Furthermore, the molecular mechanisms by which regulatory factors...

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Autores principales: Kent, Samantha, Brown, Kyle, Yang, Chou-hsun, Alsaihati, Njood, Tian, Christina, Wang, Haobin, Ren, Xiaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593837/
https://www.ncbi.nlm.nih.gov/pubmed/33053359
http://dx.doi.org/10.1016/j.celrep.2020.108248
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author Kent, Samantha
Brown, Kyle
Yang, Chou-hsun
Alsaihati, Njood
Tian, Christina
Wang, Haobin
Ren, Xiaojun
author_facet Kent, Samantha
Brown, Kyle
Yang, Chou-hsun
Alsaihati, Njood
Tian, Christina
Wang, Haobin
Ren, Xiaojun
author_sort Kent, Samantha
collection PubMed
description Compartmentalization by liquid-liquid phase separation is implicated in transcription. It remains unclear whether and how transcriptional condensates accelerate the search of transcriptional regulatory factors for their target sites. Furthermore, the molecular mechanisms by which regulatory factors nucleate on chromatin to assemble transcriptional condensates remain incompletely understood. The CBX-PRC1 complexes compartmentalize key developmental regulators for repression through phase-separated condensates driven by the chromobox 2 (CBX2) protein. Here, by using live-cell single-molecule imaging, we show that CBX2 nucleates on chromatin independently of H3K27me3 and CBX-PRC1. The interactions between CBX2 and DNA are essential for nucleating CBX-PRC1 on chromatin to assemble condensates. The assembled condensates shorten 3D diffusion time and reduce trials for finding specific sites through revisiting the same or adjacent sites repetitively, thereby accelerating CBX2 in searching for target sites. Overall, our data suggest a generic mechanism by which transcriptional regulatory factors nucleate to assemble condensates that accelerate their target-search process.
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spelling pubmed-75938372020-10-29 Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging Kent, Samantha Brown, Kyle Yang, Chou-hsun Alsaihati, Njood Tian, Christina Wang, Haobin Ren, Xiaojun Cell Rep Article Compartmentalization by liquid-liquid phase separation is implicated in transcription. It remains unclear whether and how transcriptional condensates accelerate the search of transcriptional regulatory factors for their target sites. Furthermore, the molecular mechanisms by which regulatory factors nucleate on chromatin to assemble transcriptional condensates remain incompletely understood. The CBX-PRC1 complexes compartmentalize key developmental regulators for repression through phase-separated condensates driven by the chromobox 2 (CBX2) protein. Here, by using live-cell single-molecule imaging, we show that CBX2 nucleates on chromatin independently of H3K27me3 and CBX-PRC1. The interactions between CBX2 and DNA are essential for nucleating CBX-PRC1 on chromatin to assemble condensates. The assembled condensates shorten 3D diffusion time and reduce trials for finding specific sites through revisiting the same or adjacent sites repetitively, thereby accelerating CBX2 in searching for target sites. Overall, our data suggest a generic mechanism by which transcriptional regulatory factors nucleate to assemble condensates that accelerate their target-search process. 2020-10-13 /pmc/articles/PMC7593837/ /pubmed/33053359 http://dx.doi.org/10.1016/j.celrep.2020.108248 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kent, Samantha
Brown, Kyle
Yang, Chou-hsun
Alsaihati, Njood
Tian, Christina
Wang, Haobin
Ren, Xiaojun
Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title_full Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title_fullStr Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title_full_unstemmed Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title_short Phase-Separated Transcriptional Condensates Accelerate Target-Search Process Revealed by Live-Cell Single-Molecule Imaging
title_sort phase-separated transcriptional condensates accelerate target-search process revealed by live-cell single-molecule imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593837/
https://www.ncbi.nlm.nih.gov/pubmed/33053359
http://dx.doi.org/10.1016/j.celrep.2020.108248
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