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Forces driving the three‐dimensional folding of eukaryotic genomes

The last decade has radically renewed our understanding of higher order chromatin folding in the eukaryotic nucleus. As a result, most current models are in support of a mostly hierarchical and relatively stable folding of chromosomes dividing chromosomal territories into A‐ (active) and B‐ (inactiv...

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Autores principales: Rada‐Iglesias, Alvaro, Grosveld, Frank G, Papantonis, Argyris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024091/
https://www.ncbi.nlm.nih.gov/pubmed/29858282
http://dx.doi.org/10.15252/msb.20188214
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author Rada‐Iglesias, Alvaro
Grosveld, Frank G
Papantonis, Argyris
author_facet Rada‐Iglesias, Alvaro
Grosveld, Frank G
Papantonis, Argyris
author_sort Rada‐Iglesias, Alvaro
collection PubMed
description The last decade has radically renewed our understanding of higher order chromatin folding in the eukaryotic nucleus. As a result, most current models are in support of a mostly hierarchical and relatively stable folding of chromosomes dividing chromosomal territories into A‐ (active) and B‐ (inactive) compartments, which are then further partitioned into topologically associating domains (TADs), each of which is made up from multiple loops stabilized mainly by the CTCF and cohesin chromatin‐binding complexes. Nonetheless, the structure‐to‐function relationship of eukaryotic genomes is still not well understood. Here, we focus on recent work highlighting the biophysical and regulatory forces that contribute to the spatial organization of genomes, and we propose that the various conformations that chromatin assumes are not so much the result of a linear hierarchy, but rather of both converging and conflicting dynamic forces that act on it.
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spelling pubmed-60240912018-07-30 Forces driving the three‐dimensional folding of eukaryotic genomes Rada‐Iglesias, Alvaro Grosveld, Frank G Papantonis, Argyris Mol Syst Biol Reviews The last decade has radically renewed our understanding of higher order chromatin folding in the eukaryotic nucleus. As a result, most current models are in support of a mostly hierarchical and relatively stable folding of chromosomes dividing chromosomal territories into A‐ (active) and B‐ (inactive) compartments, which are then further partitioned into topologically associating domains (TADs), each of which is made up from multiple loops stabilized mainly by the CTCF and cohesin chromatin‐binding complexes. Nonetheless, the structure‐to‐function relationship of eukaryotic genomes is still not well understood. Here, we focus on recent work highlighting the biophysical and regulatory forces that contribute to the spatial organization of genomes, and we propose that the various conformations that chromatin assumes are not so much the result of a linear hierarchy, but rather of both converging and conflicting dynamic forces that act on it. John Wiley and Sons Inc. 2018-06-01 /pmc/articles/PMC6024091/ /pubmed/29858282 http://dx.doi.org/10.15252/msb.20188214 Text en © 2018 The Authors. Published under the terms of the CC BY 4.0 license 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
Rada‐Iglesias, Alvaro
Grosveld, Frank G
Papantonis, Argyris
Forces driving the three‐dimensional folding of eukaryotic genomes
title Forces driving the three‐dimensional folding of eukaryotic genomes
title_full Forces driving the three‐dimensional folding of eukaryotic genomes
title_fullStr Forces driving the three‐dimensional folding of eukaryotic genomes
title_full_unstemmed Forces driving the three‐dimensional folding of eukaryotic genomes
title_short Forces driving the three‐dimensional folding of eukaryotic genomes
title_sort forces driving the three‐dimensional folding of eukaryotic genomes
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024091/
https://www.ncbi.nlm.nih.gov/pubmed/29858282
http://dx.doi.org/10.15252/msb.20188214
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