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ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster
DNA damage response (DDR) pathways in keto-enol genotoxicity have not been characterized, and few studies have reported genotoxic effects in non-target organisms. The present study shows that concentrations of 11.2, 22.4, 37.3 mg/L of Movento(®) 240SC and 12.3, 24.6, 41.1 mg/L of Envidor(®) 240SC fo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535977/ https://www.ncbi.nlm.nih.gov/pubmed/37755764 http://dx.doi.org/10.3390/toxics11090754 |
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author | González-Marín, Berenyce Calderón-Segura, María Elena Sekelsky, Jeff |
author_facet | González-Marín, Berenyce Calderón-Segura, María Elena Sekelsky, Jeff |
author_sort | González-Marín, Berenyce |
collection | PubMed |
description | DNA damage response (DDR) pathways in keto-enol genotoxicity have not been characterized, and few studies have reported genotoxic effects in non-target organisms. The present study shows that concentrations of 11.2, 22.4, 37.3 mg/L of Movento(®) 240SC and 12.3, 24.6, 41.1 mg/L of Envidor(®) 240SC for 72 h oral exposure induced DSBs by significantly increasing the percentage of γH2AV expression in regions 2b and 3 from the germarium of wild type females of Drosophila melanogaster Oregon R, compared to the control group (0.0 mg/L of insecticides), via confocal immunofluorescence microscopy. The comparison between both insecticides’ reveals that only the Envidor(®) 240SC induces concentration-dependent DNA damage, as well as structural changes in the germarium. We determined that the DDR induced by Movento(®) 240SC depends on the activation of the ATM(tefu), Chk1(grp) and Chk2(lok) kinases by significantly increasing the percentage of expression of γH2AV in regions 2b and 3 of the germarium, and that ATR(mei−29D) and p53(dp53) kinases only respond at the highest concentration of 37.3 mg/L of Movento(®) 240SC. With the Envidor(®) 240SC insecticide, we determined that the DDR depends on the activation of the ATR(mei−29D)/Chk1(grp) and ATM(tefu)/Chk2(lok) kinases, and p53(dp53) by significantly increasing the percentage of expression of γH2AV in the germarium. |
format | Online Article Text |
id | pubmed-10535977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105359772023-09-29 ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster González-Marín, Berenyce Calderón-Segura, María Elena Sekelsky, Jeff Toxics Article DNA damage response (DDR) pathways in keto-enol genotoxicity have not been characterized, and few studies have reported genotoxic effects in non-target organisms. The present study shows that concentrations of 11.2, 22.4, 37.3 mg/L of Movento(®) 240SC and 12.3, 24.6, 41.1 mg/L of Envidor(®) 240SC for 72 h oral exposure induced DSBs by significantly increasing the percentage of γH2AV expression in regions 2b and 3 from the germarium of wild type females of Drosophila melanogaster Oregon R, compared to the control group (0.0 mg/L of insecticides), via confocal immunofluorescence microscopy. The comparison between both insecticides’ reveals that only the Envidor(®) 240SC induces concentration-dependent DNA damage, as well as structural changes in the germarium. We determined that the DDR induced by Movento(®) 240SC depends on the activation of the ATM(tefu), Chk1(grp) and Chk2(lok) kinases by significantly increasing the percentage of expression of γH2AV in regions 2b and 3 of the germarium, and that ATR(mei−29D) and p53(dp53) kinases only respond at the highest concentration of 37.3 mg/L of Movento(®) 240SC. With the Envidor(®) 240SC insecticide, we determined that the DDR depends on the activation of the ATR(mei−29D)/Chk1(grp) and ATM(tefu)/Chk2(lok) kinases, and p53(dp53) by significantly increasing the percentage of expression of γH2AV in the germarium. MDPI 2023-09-06 /pmc/articles/PMC10535977/ /pubmed/37755764 http://dx.doi.org/10.3390/toxics11090754 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article González-Marín, Berenyce Calderón-Segura, María Elena Sekelsky, Jeff ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title | ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title_full | ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title_fullStr | ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title_full_unstemmed | ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title_short | ATM/Chk2 and ATR/Chk1 Pathways Respond to DNA Damage Induced by Movento(®) 240SC and Envidor(®) 240SC Keto-Enol Insecticides in the Germarium of Drosophila melanogaster |
title_sort | atm/chk2 and atr/chk1 pathways respond to dna damage induced by movento(®) 240sc and envidor(®) 240sc keto-enol insecticides in the germarium of drosophila melanogaster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10535977/ https://www.ncbi.nlm.nih.gov/pubmed/37755764 http://dx.doi.org/10.3390/toxics11090754 |
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