Spatial and topological organization of DNA chains induced by gene co-localization.

Transcriptional activity has been shown to relate to the organization of chromosomes in the eukaryotic nucleus and in the bacterial nucleoid. In particular, highly transcribed genes, RNA polymerases and transcription factors gather into discrete spatial foci called transcription factories. However,...

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Main Authors: Ivan Junier, Olivier Martin, François Képès
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-02-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC2820526?pdf=render
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spelling doaj-18bdab1fc96c40d59ddeb1bc32a6865e2020-11-25T01:45:47ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582010-02-0162e100067810.1371/journal.pcbi.1000678Spatial and topological organization of DNA chains induced by gene co-localization.Ivan JunierOlivier MartinFrançois KépèsTranscriptional activity has been shown to relate to the organization of chromosomes in the eukaryotic nucleus and in the bacterial nucleoid. In particular, highly transcribed genes, RNA polymerases and transcription factors gather into discrete spatial foci called transcription factories. However, the mechanisms underlying the formation of these foci and the resulting topological order of the chromosome remain to be elucidated. Here we consider a thermodynamic framework based on a worm-like chain model of chromosomes where sparse designated sites along the DNA are able to interact whenever they are spatially close by. This is motivated by recurrent evidence that there exist physical interactions between genes that operate together. Three important results come out of this simple framework. First, the resulting formation of transcription foci can be viewed as a micro-phase separation of the interacting sites from the rest of the DNA. In this respect, a thermodynamic analysis suggests transcription factors to be appropriate candidates for mediating the physical interactions between genes. Next, numerical simulations of the polymer reveal a rich variety of phases that are associated with different topological orderings, each providing a way to increase the local concentrations of the interacting sites. Finally, the numerical results show that both one-dimensional clustering and periodic location of the binding sites along the DNA, which have been observed in several organisms, make the spatial co-localization of multiple families of genes particularly efficient.http://europepmc.org/articles/PMC2820526?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ivan Junier
Olivier Martin
François Képès
spellingShingle Ivan Junier
Olivier Martin
François Képès
Spatial and topological organization of DNA chains induced by gene co-localization.
PLoS Computational Biology
author_facet Ivan Junier
Olivier Martin
François Képès
author_sort Ivan Junier
title Spatial and topological organization of DNA chains induced by gene co-localization.
title_short Spatial and topological organization of DNA chains induced by gene co-localization.
title_full Spatial and topological organization of DNA chains induced by gene co-localization.
title_fullStr Spatial and topological organization of DNA chains induced by gene co-localization.
title_full_unstemmed Spatial and topological organization of DNA chains induced by gene co-localization.
title_sort spatial and topological organization of dna chains induced by gene co-localization.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2010-02-01
description Transcriptional activity has been shown to relate to the organization of chromosomes in the eukaryotic nucleus and in the bacterial nucleoid. In particular, highly transcribed genes, RNA polymerases and transcription factors gather into discrete spatial foci called transcription factories. However, the mechanisms underlying the formation of these foci and the resulting topological order of the chromosome remain to be elucidated. Here we consider a thermodynamic framework based on a worm-like chain model of chromosomes where sparse designated sites along the DNA are able to interact whenever they are spatially close by. This is motivated by recurrent evidence that there exist physical interactions between genes that operate together. Three important results come out of this simple framework. First, the resulting formation of transcription foci can be viewed as a micro-phase separation of the interacting sites from the rest of the DNA. In this respect, a thermodynamic analysis suggests transcription factors to be appropriate candidates for mediating the physical interactions between genes. Next, numerical simulations of the polymer reveal a rich variety of phases that are associated with different topological orderings, each providing a way to increase the local concentrations of the interacting sites. Finally, the numerical results show that both one-dimensional clustering and periodic location of the binding sites along the DNA, which have been observed in several organisms, make the spatial co-localization of multiple families of genes particularly efficient.
url http://europepmc.org/articles/PMC2820526?pdf=render
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AT oliviermartin spatialandtopologicalorganizationofdnachainsinducedbygenecolocalization
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