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Is DNA Damage Response Ready for Action Anywhere?

Organisms are continuously exposed to DNA damaging agents, consequently, cells have developed an intricate system known as the DNA damage response (DDR) in order to detect and repair DNA lesions. This response has to be rapid and accurate in order to keep genome integrity. It has been observed that...

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Detalles Bibliográficos
Autores principales: Terradas, Mariona, Martín, Marta, Hernández, Laia, Tusell, Laura, Genescà, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472763/
https://www.ncbi.nlm.nih.gov/pubmed/23109871
http://dx.doi.org/10.3390/ijms130911569
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author Terradas, Mariona
Martín, Marta
Hernández, Laia
Tusell, Laura
Genescà, Anna
author_facet Terradas, Mariona
Martín, Marta
Hernández, Laia
Tusell, Laura
Genescà, Anna
author_sort Terradas, Mariona
collection PubMed
description Organisms are continuously exposed to DNA damaging agents, consequently, cells have developed an intricate system known as the DNA damage response (DDR) in order to detect and repair DNA lesions. This response has to be rapid and accurate in order to keep genome integrity. It has been observed that the condensation state of chromatin hinders a proper DDR. However, the condensation state of chromatin is not the only barrier to DDR. In this review, we have collected data regarding the presence of DDR factors on micronuclear DNA lesions that indicate that micronuclei are almost incapable of generating an effective DDR because of defects in their nuclear envelope. Finally, considering the recent observations about the reincorporation of micronuclei to the main bulk of chromosomes, we suggest that, under certain circumstances, micronuclei carrying DNA damage might be a source of chromosome instability.
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spelling pubmed-34727632012-10-29 Is DNA Damage Response Ready for Action Anywhere? Terradas, Mariona Martín, Marta Hernández, Laia Tusell, Laura Genescà, Anna Int J Mol Sci Review Organisms are continuously exposed to DNA damaging agents, consequently, cells have developed an intricate system known as the DNA damage response (DDR) in order to detect and repair DNA lesions. This response has to be rapid and accurate in order to keep genome integrity. It has been observed that the condensation state of chromatin hinders a proper DDR. However, the condensation state of chromatin is not the only barrier to DDR. In this review, we have collected data regarding the presence of DDR factors on micronuclear DNA lesions that indicate that micronuclei are almost incapable of generating an effective DDR because of defects in their nuclear envelope. Finally, considering the recent observations about the reincorporation of micronuclei to the main bulk of chromosomes, we suggest that, under certain circumstances, micronuclei carrying DNA damage might be a source of chromosome instability. Molecular Diversity Preservation International (MDPI) 2012-09-14 /pmc/articles/PMC3472763/ /pubmed/23109871 http://dx.doi.org/10.3390/ijms130911569 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Terradas, Mariona
Martín, Marta
Hernández, Laia
Tusell, Laura
Genescà, Anna
Is DNA Damage Response Ready for Action Anywhere?
title Is DNA Damage Response Ready for Action Anywhere?
title_full Is DNA Damage Response Ready for Action Anywhere?
title_fullStr Is DNA Damage Response Ready for Action Anywhere?
title_full_unstemmed Is DNA Damage Response Ready for Action Anywhere?
title_short Is DNA Damage Response Ready for Action Anywhere?
title_sort is dna damage response ready for action anywhere?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472763/
https://www.ncbi.nlm.nih.gov/pubmed/23109871
http://dx.doi.org/10.3390/ijms130911569
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