Cargando…

Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications

As an effective and versatile strategy to compartmentalize cellular components without the need for lipid membranes, phase separation has been found to underpin a wide range of intranuclear processes, particularly those involving chromatin. Many of the unique physico-chemical properties of chromatin...

Descripción completa

Detalles Bibliográficos
Autores principales: Ng, Woei Shyuan, Sielaff, Hendrik, Zhao, Ziqing Winston
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316379/
https://www.ncbi.nlm.nih.gov/pubmed/35887384
http://dx.doi.org/10.3390/ijms23148039
_version_ 1784754799881748480
author Ng, Woei Shyuan
Sielaff, Hendrik
Zhao, Ziqing Winston
author_facet Ng, Woei Shyuan
Sielaff, Hendrik
Zhao, Ziqing Winston
author_sort Ng, Woei Shyuan
collection PubMed
description As an effective and versatile strategy to compartmentalize cellular components without the need for lipid membranes, phase separation has been found to underpin a wide range of intranuclear processes, particularly those involving chromatin. Many of the unique physico-chemical properties of chromatin-based phase condensates are harnessed by the cell to accomplish complex regulatory functions in a spatially and temporally controlled manner. Here, we survey key recent findings on the mechanistic roles of phase separation in regulating the organization and dynamics of chromatin-based molecular processes across length scales, packing states and intranuclear functions, with a particular emphasis on quantitative characterizations of these condensates enabled by advanced imaging-based approaches. By illuminating the complex interplay between chromatin and various chromatin-interacting molecular species mediated by phase separation, this review sheds light on an emerging multi-scale, multi-modal and multi-faceted landscape that hierarchically regulates the genome within the highly crowded and dynamic nuclear space. Moreover, deficiencies in existing studies also highlight the need for mechanism-specific criteria and multi-parametric approaches for the characterization of chromatin-based phase separation using complementary techniques and call for greater efforts to correlate the quantitative features of these condensates with their functional consequences in close-to-native cellular contexts.
format Online
Article
Text
id pubmed-9316379
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93163792022-07-27 Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications Ng, Woei Shyuan Sielaff, Hendrik Zhao, Ziqing Winston Int J Mol Sci Review As an effective and versatile strategy to compartmentalize cellular components without the need for lipid membranes, phase separation has been found to underpin a wide range of intranuclear processes, particularly those involving chromatin. Many of the unique physico-chemical properties of chromatin-based phase condensates are harnessed by the cell to accomplish complex regulatory functions in a spatially and temporally controlled manner. Here, we survey key recent findings on the mechanistic roles of phase separation in regulating the organization and dynamics of chromatin-based molecular processes across length scales, packing states and intranuclear functions, with a particular emphasis on quantitative characterizations of these condensates enabled by advanced imaging-based approaches. By illuminating the complex interplay between chromatin and various chromatin-interacting molecular species mediated by phase separation, this review sheds light on an emerging multi-scale, multi-modal and multi-faceted landscape that hierarchically regulates the genome within the highly crowded and dynamic nuclear space. Moreover, deficiencies in existing studies also highlight the need for mechanism-specific criteria and multi-parametric approaches for the characterization of chromatin-based phase separation using complementary techniques and call for greater efforts to correlate the quantitative features of these condensates with their functional consequences in close-to-native cellular contexts. MDPI 2022-07-21 /pmc/articles/PMC9316379/ /pubmed/35887384 http://dx.doi.org/10.3390/ijms23148039 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ng, Woei Shyuan
Sielaff, Hendrik
Zhao, Ziqing Winston
Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title_full Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title_fullStr Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title_full_unstemmed Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title_short Phase Separation-Mediated Chromatin Organization and Dynamics: From Imaging-Based Quantitative Characterizations to Functional Implications
title_sort phase separation-mediated chromatin organization and dynamics: from imaging-based quantitative characterizations to functional implications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316379/
https://www.ncbi.nlm.nih.gov/pubmed/35887384
http://dx.doi.org/10.3390/ijms23148039
work_keys_str_mv AT ngwoeishyuan phaseseparationmediatedchromatinorganizationanddynamicsfromimagingbasedquantitativecharacterizationstofunctionalimplications
AT sielaffhendrik phaseseparationmediatedchromatinorganizationanddynamicsfromimagingbasedquantitativecharacterizationstofunctionalimplications
AT zhaoziqingwinston phaseseparationmediatedchromatinorganizationanddynamicsfromimagingbasedquantitativecharacterizationstofunctionalimplications