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Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments

The aim of this study was to perform a comparative investigation of the actions of three mutagens that are widely used in plant mutagenesis using the comet-FISH technique. The comet-FISH technique was used for the analysis of DNA damage and the kinetics of repair within specific DNA sequences. FISH...

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Autores principales: Kwasniewska, Jolanta, Kwasniewski, Miroslaw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825319/
https://www.ncbi.nlm.nih.gov/pubmed/24081821
http://dx.doi.org/10.1007/s13353-013-0169-6
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author Kwasniewska, Jolanta
Kwasniewski, Miroslaw
author_facet Kwasniewska, Jolanta
Kwasniewski, Miroslaw
author_sort Kwasniewska, Jolanta
collection PubMed
description The aim of this study was to perform a comparative investigation of the actions of three mutagens that are widely used in plant mutagenesis using the comet-FISH technique. The comet-FISH technique was used for the analysis of DNA damage and the kinetics of repair within specific DNA sequences. FISH with rDNA and telomeric/centromeric DNA probes was applied to comets that were obtained from an alkaline/neutral comet assay. Migration within specific DNA sequences was analysed after treatment with two chemical mutagens-maleic hydrazide (MH) and N-nitroso-N-methylurea (MNU), and γ-rays. Barley was used as a model plant in this study. The possible utility of specific DNA sequences in a comparative assessment of the distribution of DNA damage within a plant genome was evaluated. This study proved that the comet-FISH technique is suitable for a detailed quantification of DNA damage and repair within specific DNA sequences in plant mutagenesis. The analysis of FISH signals demonstrated that the involvement of specific DNA sequences in DNA damage was different and was dependent on the mutagen used. We showed that 5S rDNA and telomeric DNA sequences are more sensitive to mutagenic treatment, which was expressed by a stronger fragmentation and migration in comparison to the other probes used in the study. We found that 5S rDNA and telomeric DNA probes are more suitable for testing the genotoxicity of environmental factors. A comparison of the involvement of specific chromosome domains in direct DNA breakage/repair and in chromosome aberration formation after mutagen treatment indicates the compatibility of the results.
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spelling pubmed-38253192013-11-21 Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments Kwasniewska, Jolanta Kwasniewski, Miroslaw J Appl Genet Plant Genetics • Original Paper The aim of this study was to perform a comparative investigation of the actions of three mutagens that are widely used in plant mutagenesis using the comet-FISH technique. The comet-FISH technique was used for the analysis of DNA damage and the kinetics of repair within specific DNA sequences. FISH with rDNA and telomeric/centromeric DNA probes was applied to comets that were obtained from an alkaline/neutral comet assay. Migration within specific DNA sequences was analysed after treatment with two chemical mutagens-maleic hydrazide (MH) and N-nitroso-N-methylurea (MNU), and γ-rays. Barley was used as a model plant in this study. The possible utility of specific DNA sequences in a comparative assessment of the distribution of DNA damage within a plant genome was evaluated. This study proved that the comet-FISH technique is suitable for a detailed quantification of DNA damage and repair within specific DNA sequences in plant mutagenesis. The analysis of FISH signals demonstrated that the involvement of specific DNA sequences in DNA damage was different and was dependent on the mutagen used. We showed that 5S rDNA and telomeric DNA sequences are more sensitive to mutagenic treatment, which was expressed by a stronger fragmentation and migration in comparison to the other probes used in the study. We found that 5S rDNA and telomeric DNA probes are more suitable for testing the genotoxicity of environmental factors. A comparison of the involvement of specific chromosome domains in direct DNA breakage/repair and in chromosome aberration formation after mutagen treatment indicates the compatibility of the results. Springer Berlin Heidelberg 2013-10-01 2013 /pmc/articles/PMC3825319/ /pubmed/24081821 http://dx.doi.org/10.1007/s13353-013-0169-6 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Plant Genetics • Original Paper
Kwasniewska, Jolanta
Kwasniewski, Miroslaw
Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title_full Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title_fullStr Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title_full_unstemmed Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title_short Comet-FISH for the evaluation of plant DNA damage after mutagenic treatments
title_sort comet-fish for the evaluation of plant dna damage after mutagenic treatments
topic Plant Genetics • Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825319/
https://www.ncbi.nlm.nih.gov/pubmed/24081821
http://dx.doi.org/10.1007/s13353-013-0169-6
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