2015
DOI: 10.1266/ggs.90.11
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Abstract: Reactive oxygen species (ROS) generated during energy production processes are a major cause of oxidative DNA damage. A DNA glycosylase encoded by the Ogg1 gene removes oxidized guanine bases and is widely conserved. However, the biological role of the gene in individual organisms has not yet been characterized in Drosophila, which is a suitable model to study the influence of oxidative damage on senescence. Here, we performed a genetic analysis to confirm that Ogg1 plays an essential role in the removal of 8-… Show more

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Cited by 6 publications
(5 citation statements)
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References 59 publications
(61 reference statements)
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“…The climbing assays, which used a fly's instinct of negative geotaxis, were carried out according to a previous protocol (Oka et al., ; Yasukawa, Nakahara, Hirai, & Inoue, ). Flies were gently tapped to the bottom of a plastic culture tube (100 mm in height and 15 mm in diameter), and the number of flies that climbed up to a marked point (50 mm height) after 6 seconds was counted.…”
Section: Methodsmentioning
confidence: 99%
“…The climbing assays, which used a fly's instinct of negative geotaxis, were carried out according to a previous protocol (Oka et al., ; Yasukawa, Nakahara, Hirai, & Inoue, ). Flies were gently tapped to the bottom of a plastic culture tube (100 mm in height and 15 mm in diameter), and the number of flies that climbed up to a marked point (50 mm height) after 6 seconds was counted.…”
Section: Methodsmentioning
confidence: 99%
“…qRT-PCR analysis was performed to determine the expression level of lamin genes and Nups genes in adult flies with induced expression of each dsRNA with a bam-Gal4 driver as described (Yasukawa et al, 2015). Total RNA was extracted from adult flies using the TRIzol reagent (Invitrogen, Carlsbad, CA, USA).…”
Section: Methodsmentioning
confidence: 99%
“…Exposure to 2000 pM of EMB affected both cell cycle regulation and DNA repair pathways. Interestingly, most of the supporting DEGs in these pathways were found to be repressed, such as DNA excision repair protein ERCC-1 ( Ercc1 ), double-strand break repair protein MRE11 ( Mre11 ) and 8-oxoguanine DNA glycosylase ( Ogg1 ), albeit these genes were normally up-regulated in arthropods after exposure to genotoxic agents. Suppression of DNA repair may be caused by different mechanisms. One possible explanation may be the unbalanced expression between the proliferating cell nuclear antigen ( Pcna ) and cyclin-dependent kinase inhibitor 1 ( P21 ) genes which are upstream regulators of DNA repair signaling. , Interestingly, the Pcna gene was down-regulated in a concentration-dependent manner, whereas the double-strand-break repair protein rad21 homologue ( Vtd ) gene were slightly up-regulated after exposure to 500 pM EMB and marginally down-regulated by exposure to 2000 pM EMB in this study, suggesting that suppression of DNA repair signaling may likely be a consequence of abnormal expression of these genes in D. magna after exposure to EMB.…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, most of the supporting DEGs in these pathways were found to be repressed, such as DNA excision repair protein ERCC-1 (Ercc1), double-strand break repair protein MRE11 (Mre11) and 8-oxoguanine DNA glycosylase (Ogg1), albeit these genes were normally up-regulated in arthropods after exposure to genotoxic agents. [54][55][56][57][58] Suppression of DNA repair may be caused by different mechanisms. One possible explanation may be the unbalanced expression between the proliferating cell nuclear antigen (PCNA) and cyclin-dependent kinase inhibitor 1 (P21) genes which are upstream regulators of DNA repair signaling.…”
Section: Toxic Mechanisms Activation Of Ligand-gated Chloride Channels In Line With the Previously Proposedmentioning
confidence: 99%