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Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods
The Waddington landscape provides an intuitive metaphor to view development as a ball rolling down the hill, with distinct phenotypes as basins and differentiation pathways as valleys. Since, at a molecular level, cell differentiation arises from interactions among the genes, a mathematical definiti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862759/ https://www.ncbi.nlm.nih.gov/pubmed/33552146 http://dx.doi.org/10.3389/fgene.2020.636724 |
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author | Sood, Amogh Zhang, Bin |
author_facet | Sood, Amogh Zhang, Bin |
author_sort | Sood, Amogh |
collection | PubMed |
description | The Waddington landscape provides an intuitive metaphor to view development as a ball rolling down the hill, with distinct phenotypes as basins and differentiation pathways as valleys. Since, at a molecular level, cell differentiation arises from interactions among the genes, a mathematical definition for the Waddington landscape can, in principle, be obtained by studying the gene regulatory networks. For eukaryotes, gene regulation is inextricably and intimately linked to histone modifications. However, the impact of such modifications on both landscape topography and stability of attractor states is not fully understood. In this work, we introduced a minimal kinetic model for gene regulation that combines the impact of both histone modifications and transcription factors. We further developed an approximation scheme based on variational principles to solve the corresponding master equation in a second quantized framework. By analyzing the steady-state solutions at various parameter regimes, we found that histone modification kinetics can significantly alter the behavior of a genetic network, resulting in qualitative changes in gene expression profiles. The emerging epigenetic landscape captures the delicate interplay between transcription factors and histone modifications in driving cell-fate decisions. |
format | Online Article Text |
id | pubmed-7862759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78627592021-02-06 Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods Sood, Amogh Zhang, Bin Front Genet Genetics The Waddington landscape provides an intuitive metaphor to view development as a ball rolling down the hill, with distinct phenotypes as basins and differentiation pathways as valleys. Since, at a molecular level, cell differentiation arises from interactions among the genes, a mathematical definition for the Waddington landscape can, in principle, be obtained by studying the gene regulatory networks. For eukaryotes, gene regulation is inextricably and intimately linked to histone modifications. However, the impact of such modifications on both landscape topography and stability of attractor states is not fully understood. In this work, we introduced a minimal kinetic model for gene regulation that combines the impact of both histone modifications and transcription factors. We further developed an approximation scheme based on variational principles to solve the corresponding master equation in a second quantized framework. By analyzing the steady-state solutions at various parameter regimes, we found that histone modification kinetics can significantly alter the behavior of a genetic network, resulting in qualitative changes in gene expression profiles. The emerging epigenetic landscape captures the delicate interplay between transcription factors and histone modifications in driving cell-fate decisions. Frontiers Media S.A. 2021-01-22 /pmc/articles/PMC7862759/ /pubmed/33552146 http://dx.doi.org/10.3389/fgene.2020.636724 Text en Copyright © 2021 Sood and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Sood, Amogh Zhang, Bin Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title | Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title_full | Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title_fullStr | Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title_full_unstemmed | Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title_short | Quantifying the Stability of Coupled Genetic and Epigenetic Switches With Variational Methods |
title_sort | quantifying the stability of coupled genetic and epigenetic switches with variational methods |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862759/ https://www.ncbi.nlm.nih.gov/pubmed/33552146 http://dx.doi.org/10.3389/fgene.2020.636724 |
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