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Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond

Micronuclei (MN) are extra-nuclear bodies that contain damaged chromosome fragments and/or whole chromosomes that were not incorporated into the nucleus after cell division. MN can be induced by defects in the cell repair machinery and accumulation of DNA damages and chromosomal aberrations. A varie...

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Autores principales: Luzhna, Lidiya, Kathiria, Palak, Kovalchuk, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708156/
https://www.ncbi.nlm.nih.gov/pubmed/23874352
http://dx.doi.org/10.3389/fgene.2013.00131
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author Luzhna, Lidiya
Kathiria, Palak
Kovalchuk, Olga
author_facet Luzhna, Lidiya
Kathiria, Palak
Kovalchuk, Olga
author_sort Luzhna, Lidiya
collection PubMed
description Micronuclei (MN) are extra-nuclear bodies that contain damaged chromosome fragments and/or whole chromosomes that were not incorporated into the nucleus after cell division. MN can be induced by defects in the cell repair machinery and accumulation of DNA damages and chromosomal aberrations. A variety of genotoxic agents may induce MN formation leading to cell death, genomic instability, or cancer development. In this review, the genetic and epigenetic mechanisms of MN formation after various clastogenic and aneugenic effects on cell division and cell cycle are described. The knowledge accumulated in literature on cytotoxicity of various genotoxins is precisely reflected and individual sensitivity to MN formation due to single gene polymorphisms is discussed. The importance of rapid MN scoring with respect to the cytokinesis-block micronucleus assay is also evaluated.
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spelling pubmed-37081562013-07-19 Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond Luzhna, Lidiya Kathiria, Palak Kovalchuk, Olga Front Genet Genetics Micronuclei (MN) are extra-nuclear bodies that contain damaged chromosome fragments and/or whole chromosomes that were not incorporated into the nucleus after cell division. MN can be induced by defects in the cell repair machinery and accumulation of DNA damages and chromosomal aberrations. A variety of genotoxic agents may induce MN formation leading to cell death, genomic instability, or cancer development. In this review, the genetic and epigenetic mechanisms of MN formation after various clastogenic and aneugenic effects on cell division and cell cycle are described. The knowledge accumulated in literature on cytotoxicity of various genotoxins is precisely reflected and individual sensitivity to MN formation due to single gene polymorphisms is discussed. The importance of rapid MN scoring with respect to the cytokinesis-block micronucleus assay is also evaluated. Frontiers Media S.A. 2013-07-11 /pmc/articles/PMC3708156/ /pubmed/23874352 http://dx.doi.org/10.3389/fgene.2013.00131 Text en Copyright © Luzhna, Kathiria and Kovalchuk. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Genetics
Luzhna, Lidiya
Kathiria, Palak
Kovalchuk, Olga
Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title_full Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title_fullStr Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title_full_unstemmed Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title_short Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
title_sort micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708156/
https://www.ncbi.nlm.nih.gov/pubmed/23874352
http://dx.doi.org/10.3389/fgene.2013.00131
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