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Chromosome positioning from activity-based segregation

Chromosomes within eukaryotic cell nuclei at interphase are not positioned at random, since gene-rich chromosomes are predominantly found towards the interior of the cell nucleus across a number of cell types. The physical mechanisms that could drive and maintain the spatial segregation of chromosom...

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Autores principales: Ganai, Nirmalendu, Sengupta, Surajit, Menon, Gautam I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985638/
https://www.ncbi.nlm.nih.gov/pubmed/24459132
http://dx.doi.org/10.1093/nar/gkt1417
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author Ganai, Nirmalendu
Sengupta, Surajit
Menon, Gautam I.
author_facet Ganai, Nirmalendu
Sengupta, Surajit
Menon, Gautam I.
author_sort Ganai, Nirmalendu
collection PubMed
description Chromosomes within eukaryotic cell nuclei at interphase are not positioned at random, since gene-rich chromosomes are predominantly found towards the interior of the cell nucleus across a number of cell types. The physical mechanisms that could drive and maintain the spatial segregation of chromosomes based on gene density are unknown. Here, we identify a mechanism for such segregation, showing that the territorial organization of chromosomes, another central feature of nuclear organization, emerges naturally from our model. Our computer simulations indicate that gene density-dependent radial segregation of chromosomes arises as a robust consequence of differences in non-equilibrium activity across chromosomes. Arguing that such differences originate in the inhomogeneous distribution of ATP-dependent chromatin remodeling and transcription machinery on each chromosome, we show that a variety of non-random positional distributions emerge through the interplay of such activity, nuclear shape and specific interactions of chromosomes with the nuclear envelope. Results from our model are in reasonable agreement with experimental data and we make a number of predictions that can be tested in experiments.
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spelling pubmed-39856382014-04-18 Chromosome positioning from activity-based segregation Ganai, Nirmalendu Sengupta, Surajit Menon, Gautam I. Nucleic Acids Res Computational Biology Chromosomes within eukaryotic cell nuclei at interphase are not positioned at random, since gene-rich chromosomes are predominantly found towards the interior of the cell nucleus across a number of cell types. The physical mechanisms that could drive and maintain the spatial segregation of chromosomes based on gene density are unknown. Here, we identify a mechanism for such segregation, showing that the territorial organization of chromosomes, another central feature of nuclear organization, emerges naturally from our model. Our computer simulations indicate that gene density-dependent radial segregation of chromosomes arises as a robust consequence of differences in non-equilibrium activity across chromosomes. Arguing that such differences originate in the inhomogeneous distribution of ATP-dependent chromatin remodeling and transcription machinery on each chromosome, we show that a variety of non-random positional distributions emerge through the interplay of such activity, nuclear shape and specific interactions of chromosomes with the nuclear envelope. Results from our model are in reasonable agreement with experimental data and we make a number of predictions that can be tested in experiments. Oxford University Press 2014-04 2014-01-22 /pmc/articles/PMC3985638/ /pubmed/24459132 http://dx.doi.org/10.1093/nar/gkt1417 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Computational Biology
Ganai, Nirmalendu
Sengupta, Surajit
Menon, Gautam I.
Chromosome positioning from activity-based segregation
title Chromosome positioning from activity-based segregation
title_full Chromosome positioning from activity-based segregation
title_fullStr Chromosome positioning from activity-based segregation
title_full_unstemmed Chromosome positioning from activity-based segregation
title_short Chromosome positioning from activity-based segregation
title_sort chromosome positioning from activity-based segregation
topic Computational Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985638/
https://www.ncbi.nlm.nih.gov/pubmed/24459132
http://dx.doi.org/10.1093/nar/gkt1417
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