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Chromatin‐modifying drugs and metabolites in cell fate control

For multicellular organisms, it is essential to produce a variety of specialized cells to perform a dazzling panoply of functions. Chromatin plays a vital role in determining cellular identities, and it dynamically regulates gene expression in response to changing nutrient metabolism and environment...

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Detalles Bibliográficos
Autores principales: Yao, Ziyue, Chen, Yu, Cao, Wenhua, Shyh‐Chang, Ng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653270/
https://www.ncbi.nlm.nih.gov/pubmed/32979011
http://dx.doi.org/10.1111/cpr.12898
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author Yao, Ziyue
Chen, Yu
Cao, Wenhua
Shyh‐Chang, Ng
author_facet Yao, Ziyue
Chen, Yu
Cao, Wenhua
Shyh‐Chang, Ng
author_sort Yao, Ziyue
collection PubMed
description For multicellular organisms, it is essential to produce a variety of specialized cells to perform a dazzling panoply of functions. Chromatin plays a vital role in determining cellular identities, and it dynamically regulates gene expression in response to changing nutrient metabolism and environmental conditions. Intermediates produced by cellular metabolic pathways are used as cofactors or substrates for chromatin modification. Drug analogues of metabolites that regulate chromatin‐modifying enzyme reactions can also regulate cell fate by adjusting chromatin organization. In recent years, there have been many studies about how chromatin‐modifying drug molecules or metabolites can interact with chromatin to regulate cell fate. In this review, we systematically discuss how DNA and histone‐modifying molecules alter cell fate by regulating chromatin conformation and propose a mechanistic model that explains the process of cell fate transitions in a concise and qualitative manner.
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spelling pubmed-76532702020-11-16 Chromatin‐modifying drugs and metabolites in cell fate control Yao, Ziyue Chen, Yu Cao, Wenhua Shyh‐Chang, Ng Cell Prolif Reviews For multicellular organisms, it is essential to produce a variety of specialized cells to perform a dazzling panoply of functions. Chromatin plays a vital role in determining cellular identities, and it dynamically regulates gene expression in response to changing nutrient metabolism and environmental conditions. Intermediates produced by cellular metabolic pathways are used as cofactors or substrates for chromatin modification. Drug analogues of metabolites that regulate chromatin‐modifying enzyme reactions can also regulate cell fate by adjusting chromatin organization. In recent years, there have been many studies about how chromatin‐modifying drug molecules or metabolites can interact with chromatin to regulate cell fate. In this review, we systematically discuss how DNA and histone‐modifying molecules alter cell fate by regulating chromatin conformation and propose a mechanistic model that explains the process of cell fate transitions in a concise and qualitative manner. John Wiley and Sons Inc. 2020-09-26 /pmc/articles/PMC7653270/ /pubmed/32979011 http://dx.doi.org/10.1111/cpr.12898 Text en © 2020 The Authors. Cell Proliferation published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Yao, Ziyue
Chen, Yu
Cao, Wenhua
Shyh‐Chang, Ng
Chromatin‐modifying drugs and metabolites in cell fate control
title Chromatin‐modifying drugs and metabolites in cell fate control
title_full Chromatin‐modifying drugs and metabolites in cell fate control
title_fullStr Chromatin‐modifying drugs and metabolites in cell fate control
title_full_unstemmed Chromatin‐modifying drugs and metabolites in cell fate control
title_short Chromatin‐modifying drugs and metabolites in cell fate control
title_sort chromatin‐modifying drugs and metabolites in cell fate control
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653270/
https://www.ncbi.nlm.nih.gov/pubmed/32979011
http://dx.doi.org/10.1111/cpr.12898
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