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Updated: Aug 6, 2025

In Vivo Biosensor Tracks Non-apoptotic Caspase Activity in Drosophila
Published on: November 27, 2016
Mutation and apoptosis are well-coordinated for protecting against DNA damage-inducing toxicity in Drosophila
Megumi Toyoshima-Sasatani1,2, Fumika Imura1, Yuko Hamatake1
1Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Tsushima, 700-8530, Japan.
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.
Insights
Apoptosis and somatic cell mutations are linked, with their balance depending on DNA damage type. Mutated cells may replace apoptotic cells, influencing organism survival.
Area of Science:
- Cellular Biology
- Genetics
- Toxicology
Background:
- Apoptosis removes damaged cells, while mutation is a survival mechanism for DNA lesions.
- The direct relationship between apoptosis and mutagen-induced somatic cell mutations is not well-understood.
Purpose of the Study:
- To investigate the correlation between apoptosis and somatic cell mutations induced by various mutagenic factors.
- To explore how apoptosis influences the behavior of mutated cells.
Main Methods:
- Somatic cell mutations detected using the Drosophila wing-spot test.
- Apoptosis observed in wing discs via acridine orange staining.
- DNA repair-deficient Drosophila strains used to analyze repair mechanisms.
Main Results:
- Apoptotic frequency and mutagenicity increased dose-dependently with chemical mutagens, UV, and X-ray at non-toxic doses.
- The correlation between apoptosis and mutagenicity differed in DNA repair-deficient strains compared to wild-type.
- Spot size increased with MNU or X-ray treatment due to potential replacement of apoptotic cells by rapidly dividing mutated cells, but not with UV irradiation.
Conclusions:
- Apoptosis and mutation are coordinated, with their balance influenced by DNA damage type.
- Mutated cells may replace apoptotic cells, leading to enlarged spot sizes after certain mutagen treatments.
- The interplay between mutation, apoptosis, and cell growth is crucial for organismal survival in response to DNA damage.
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