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Chromosome territories reposition during DNA damage-repair response

BACKGROUND: Local higher-order chromatin structure, dynamics and composition of the DNA are known to determine double-strand break frequencies and the efficiency of repair. However, how DNA damage response affects the spatial organization of chromosome territories is still unexplored. RESULTS: Our r...

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Autores principales: Mehta, Ishita S, Kulashreshtha, Mugdha, Chakraborty, Sandeep, Kolthur-Seetharam, Ullas, Rao, Basuthkar J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062845/
https://www.ncbi.nlm.nih.gov/pubmed/24330859
http://dx.doi.org/10.1186/gb-2013-14-12-r135
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author Mehta, Ishita S
Kulashreshtha, Mugdha
Chakraborty, Sandeep
Kolthur-Seetharam, Ullas
Rao, Basuthkar J
author_facet Mehta, Ishita S
Kulashreshtha, Mugdha
Chakraborty, Sandeep
Kolthur-Seetharam, Ullas
Rao, Basuthkar J
author_sort Mehta, Ishita S
collection PubMed
description BACKGROUND: Local higher-order chromatin structure, dynamics and composition of the DNA are known to determine double-strand break frequencies and the efficiency of repair. However, how DNA damage response affects the spatial organization of chromosome territories is still unexplored. RESULTS: Our report investigates the effect of DNA damage on the spatial organization of chromosome territories within interphase nuclei of human cells. We show that DNA damage induces a large-scale spatial repositioning of chromosome territories that are relatively gene dense. This response is dose dependent, and involves territories moving from the nuclear interior to the periphery and vice versa. Furthermore, we have found that chromosome territory repositioning is contingent upon double-strand break recognition and damage sensing. Importantly, our results suggest that this is a reversible process where, following repair, chromosome territories re-occupy positions similar to those in undamaged control cells. CONCLUSIONS: Thus, our report for the first time highlights DNA damage-dependent spatial reorganization of whole chromosomes, which might be an integral aspect of cellular damage response.
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spelling pubmed-40628452014-06-19 Chromosome territories reposition during DNA damage-repair response Mehta, Ishita S Kulashreshtha, Mugdha Chakraborty, Sandeep Kolthur-Seetharam, Ullas Rao, Basuthkar J Genome Biol Research BACKGROUND: Local higher-order chromatin structure, dynamics and composition of the DNA are known to determine double-strand break frequencies and the efficiency of repair. However, how DNA damage response affects the spatial organization of chromosome territories is still unexplored. RESULTS: Our report investigates the effect of DNA damage on the spatial organization of chromosome territories within interphase nuclei of human cells. We show that DNA damage induces a large-scale spatial repositioning of chromosome territories that are relatively gene dense. This response is dose dependent, and involves territories moving from the nuclear interior to the periphery and vice versa. Furthermore, we have found that chromosome territory repositioning is contingent upon double-strand break recognition and damage sensing. Importantly, our results suggest that this is a reversible process where, following repair, chromosome territories re-occupy positions similar to those in undamaged control cells. CONCLUSIONS: Thus, our report for the first time highlights DNA damage-dependent spatial reorganization of whole chromosomes, which might be an integral aspect of cellular damage response. BioMed Central 2013 2013-12-13 /pmc/articles/PMC4062845/ /pubmed/24330859 http://dx.doi.org/10.1186/gb-2013-14-12-r135 Text en Copyright © 2013 Mehta et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mehta, Ishita S
Kulashreshtha, Mugdha
Chakraborty, Sandeep
Kolthur-Seetharam, Ullas
Rao, Basuthkar J
Chromosome territories reposition during DNA damage-repair response
title Chromosome territories reposition during DNA damage-repair response
title_full Chromosome territories reposition during DNA damage-repair response
title_fullStr Chromosome territories reposition during DNA damage-repair response
title_full_unstemmed Chromosome territories reposition during DNA damage-repair response
title_short Chromosome territories reposition during DNA damage-repair response
title_sort chromosome territories reposition during dna damage-repair response
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062845/
https://www.ncbi.nlm.nih.gov/pubmed/24330859
http://dx.doi.org/10.1186/gb-2013-14-12-r135
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