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Toyoshima-Sasatani, Megumi Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
Imura, Fumika Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
Hamatake, Yuko Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University
Fukunaga, Akihiro School of Nursing, Osaka City University
Negishi, Tomoe Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
Abstract
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.
Keywords
Drosophila
Apoptosis
Mutation
Larval wing disc
X-ray
Ultraviolet
Alkylating agents
Tobacco smoke
Acridine orange
BrdU
Note
The version of record of this article, first published in Genes and Environment, is available online at Publisher’s website: http://dx.doi.org/10.1186/s41021-023-00267-4
Published Date
2023-03-23
Publication Title
Genes and Environment
Volume
volume45
Issue
issue1
Publisher
Springer Science and Business Media LLC
Start Page
11
ISSN
1880-7062
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2023.
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isVersionOf https://doi.org/10.1186/s41021-023-00267-4
License
http://creativecommons.org/licenses/by/4.0/
Citation
Toyoshima-Sasatani, M., Imura, F., Hamatake, Y. et al. Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila. Genes and Environ 45, 11 (2023). https://doi.org/10.1186/s41021-023-00267-4
Funder Name
Sumitomo Foundation