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Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila
BACKGROUND: Apoptotic cell death is an important survival system for multicellular organisms because it removes damaged cells. Mutation is also a survival method for dealing with damaged cells in multicellular and also unicellular organisms, when DNA lesions are not removed. However, to the best of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035180/ https://www.ncbi.nlm.nih.gov/pubmed/36949493 http://dx.doi.org/10.1186/s41021-023-00267-4 |
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author | Toyoshima-Sasatani, Megumi Imura, Fumika Hamatake, Yuko Fukunaga, Akihiro Negishi, Tomoe |
author_facet | Toyoshima-Sasatani, Megumi Imura, Fumika Hamatake, Yuko Fukunaga, Akihiro Negishi, Tomoe |
author_sort | Toyoshima-Sasatani, Megumi |
collection | PubMed |
description | BACKGROUND: Apoptotic cell death is an important survival system for multicellular organisms because it removes damaged cells. Mutation is also a survival method for dealing with damaged cells in multicellular and also unicellular organisms, when DNA lesions are not removed. However, to the best of our knowledge, no reports have comprehensively explored the direct relationship between apoptosis and somatic cell mutations induced by various mutagenic factors. RESULTS: Mutation was examined by the wing-spot test, which is used to detect somatic cell mutations, including chromosomal recombination. Apoptosis was observed in the wing discs by acridine orange staining in situ. After treatment with chemical mutagens, ultraviolet light (UV), and X-ray, both the apoptotic frequency and mutagenic activity increased in a dose-dependent manner at non-toxic doses. When we used DNA repair-deficient Drosophila strains, the correlation coefficient of the relationship between apoptosis and mutagenicity, differed from that of the wild-type. To explore how apoptosis affects the behavior of mutated cells, we determined the spot size, i.e., the number of mutated cells in a spot. In parallel with an increase in apoptosis, the spot size increased with MNU or X-ray treatment dose-dependently; however, this increase was not seen with UV irradiation. In addition, BrdU incorporation, an indicator of cell proliferation, in the wing discs was suppressed at 6 h, with peak at 12 h post-treatment with X-ray, and that it started to increase again at 24 h; however, this was not seen with UV irradiation. CONCLUSION: Damage-induced apoptosis and mutation might be coordinated with each other, and the frequency of apoptosis and mutagenicity are balanced depending on the type of DNA damage. From the data of the spot size and BrdU incorporation, it is possible that mutated cells replace apoptotic cells due to their high frequency of cell division, resulting in enlargement of the spot size after MNU or X-ray treatment. We consider that the induction of mutation, apoptosis, and/or cell growth varies in multi-cellular organisms depending on the type of the mutagens, and that their balance and coordination have an important function to counter DNA damage for the survival of the organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41021-023-00267-4. |
format | Online Article Text |
id | pubmed-10035180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100351802023-03-24 Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila Toyoshima-Sasatani, Megumi Imura, Fumika Hamatake, Yuko Fukunaga, Akihiro Negishi, Tomoe Genes Environ Research BACKGROUND: Apoptotic cell death is an important survival system for multicellular organisms because it removes damaged cells. Mutation is also a survival method for dealing with damaged cells in multicellular and also unicellular organisms, when DNA lesions are not removed. However, to the best of our knowledge, no reports have comprehensively explored the direct relationship between apoptosis and somatic cell mutations induced by various mutagenic factors. RESULTS: Mutation was examined by the wing-spot test, which is used to detect somatic cell mutations, including chromosomal recombination. Apoptosis was observed in the wing discs by acridine orange staining in situ. After treatment with chemical mutagens, ultraviolet light (UV), and X-ray, both the apoptotic frequency and mutagenic activity increased in a dose-dependent manner at non-toxic doses. When we used DNA repair-deficient Drosophila strains, the correlation coefficient of the relationship between apoptosis and mutagenicity, differed from that of the wild-type. To explore how apoptosis affects the behavior of mutated cells, we determined the spot size, i.e., the number of mutated cells in a spot. In parallel with an increase in apoptosis, the spot size increased with MNU or X-ray treatment dose-dependently; however, this increase was not seen with UV irradiation. In addition, BrdU incorporation, an indicator of cell proliferation, in the wing discs was suppressed at 6 h, with peak at 12 h post-treatment with X-ray, and that it started to increase again at 24 h; however, this was not seen with UV irradiation. CONCLUSION: Damage-induced apoptosis and mutation might be coordinated with each other, and the frequency of apoptosis and mutagenicity are balanced depending on the type of DNA damage. From the data of the spot size and BrdU incorporation, it is possible that mutated cells replace apoptotic cells due to their high frequency of cell division, resulting in enlargement of the spot size after MNU or X-ray treatment. We consider that the induction of mutation, apoptosis, and/or cell growth varies in multi-cellular organisms depending on the type of the mutagens, and that their balance and coordination have an important function to counter DNA damage for the survival of the organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41021-023-00267-4. BioMed Central 2023-03-23 /pmc/articles/PMC10035180/ /pubmed/36949493 http://dx.doi.org/10.1186/s41021-023-00267-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Toyoshima-Sasatani, Megumi Imura, Fumika Hamatake, Yuko Fukunaga, Akihiro Negishi, Tomoe Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title | Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title_full | Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title_fullStr | Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title_full_unstemmed | Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title_short | Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila |
title_sort | mutation and apoptosis are well-coordinated for protecting against dna damage-inducing toxicity in drosophila |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035180/ https://www.ncbi.nlm.nih.gov/pubmed/36949493 http://dx.doi.org/10.1186/s41021-023-00267-4 |
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