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MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells
The relationship between stochastic transcriptional bursts and dynamic 3D chromatin states is not well understood. Using an innovated, ultra-sensitive technique, we address here enigmatic features underlying the communications between MYC and its enhancers in relation to the transcriptional process....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641766/ https://www.ncbi.nlm.nih.gov/pubmed/33051686 http://dx.doi.org/10.1093/nar/gkaa817 |
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author | Sumida, Noriyuki Sifakis, Emmanouil G Kiani, Narsis A Ronnegren, Anna Lewandowska Scholz, Barbara A Vestlund, Johanna Gomez-Cabrero, David Tegner, Jesper Göndör, Anita Ohlsson, Rolf |
author_facet | Sumida, Noriyuki Sifakis, Emmanouil G Kiani, Narsis A Ronnegren, Anna Lewandowska Scholz, Barbara A Vestlund, Johanna Gomez-Cabrero, David Tegner, Jesper Göndör, Anita Ohlsson, Rolf |
author_sort | Sumida, Noriyuki |
collection | PubMed |
description | The relationship between stochastic transcriptional bursts and dynamic 3D chromatin states is not well understood. Using an innovated, ultra-sensitive technique, we address here enigmatic features underlying the communications between MYC and its enhancers in relation to the transcriptional process. MYC thus interacts with its flanking enhancers in a mutually exclusive manner documenting that enhancer hubs impinging on MYC detected in large cell populations likely do not exist in single cells. Dynamic encounters with pathologically activated enhancers responsive to a range of environmental cues, involved <10% of active MYC alleles at any given time in colon cancer cells. Being the most central node of the chromatin network, MYC itself likely drives its communications with flanking enhancers, rather than vice versa. We submit that these features underlie an acquired ability of MYC to become dynamically activated in response to a diverse range of environmental cues encountered by the cell during the neoplastic process. |
format | Online Article Text |
id | pubmed-7641766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76417662020-11-10 MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells Sumida, Noriyuki Sifakis, Emmanouil G Kiani, Narsis A Ronnegren, Anna Lewandowska Scholz, Barbara A Vestlund, Johanna Gomez-Cabrero, David Tegner, Jesper Göndör, Anita Ohlsson, Rolf Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The relationship between stochastic transcriptional bursts and dynamic 3D chromatin states is not well understood. Using an innovated, ultra-sensitive technique, we address here enigmatic features underlying the communications between MYC and its enhancers in relation to the transcriptional process. MYC thus interacts with its flanking enhancers in a mutually exclusive manner documenting that enhancer hubs impinging on MYC detected in large cell populations likely do not exist in single cells. Dynamic encounters with pathologically activated enhancers responsive to a range of environmental cues, involved <10% of active MYC alleles at any given time in colon cancer cells. Being the most central node of the chromatin network, MYC itself likely drives its communications with flanking enhancers, rather than vice versa. We submit that these features underlie an acquired ability of MYC to become dynamically activated in response to a diverse range of environmental cues encountered by the cell during the neoplastic process. Oxford University Press 2020-10-13 /pmc/articles/PMC7641766/ /pubmed/33051686 http://dx.doi.org/10.1093/nar/gkaa817 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Sumida, Noriyuki Sifakis, Emmanouil G Kiani, Narsis A Ronnegren, Anna Lewandowska Scholz, Barbara A Vestlund, Johanna Gomez-Cabrero, David Tegner, Jesper Göndör, Anita Ohlsson, Rolf MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title |
MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title_full |
MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title_fullStr |
MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title_full_unstemmed |
MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title_short |
MYC as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
title_sort | myc as a driver of stochastic chromatin networks: implications for the fitness of cancer cells |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641766/ https://www.ncbi.nlm.nih.gov/pubmed/33051686 http://dx.doi.org/10.1093/nar/gkaa817 |
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