The Comet Assay in Drosophila: A Tool to Study Interactions between DNA Repair Systems in DNA Damage Responses In Vivo and Ex Vivo

被引:1
|
作者
Rodriguez, Ruben [1 ,2 ,8 ]
Gaivao, Isabel [3 ,4 ]
Aguado, Leticia [1 ,2 ]
Espina, Marta [1 ,2 ]
Garcia, Jorge [1 ,9 ]
Martinez-Camblor, Pablo [5 ,6 ]
Sierra, L. Maria [1 ,2 ,7 ]
机构
[1] Univ Oviedo, Dept Funct Biol, Genet Area, Oviedo 33006, Spain
[2] Univ Oviedo, Oncol Univ Inst Asturias IUOPA, Oviedo 33006, Spain
[3] Univ Tras os Montes & Alto Douro, Dept Genet & Biotechnol, P-5000801 Vila Real, Portugal
[4] Univ Tras os Montes & Alto Douro, CECAV, P-5000801 Vila Real, Portugal
[5] Geisel Med Sch Dartmouth, Dept Biomed Data Sci, Hanover, NH 03755 USA
[6] Univ Autonoma Chile, Fac Hlth Sci, Provedencia 7500912, Chile
[7] Inst Sanitary Res Principal Asturias, Ave Hosp Univ, s-n, Oviedo 33011, Spain
[8] Evolut Europe, Paseo Castellana 184, Madrid 28046, Spain
[9] Hosp Infantil Univ Nino Jesus, Ave Menendez Pelayo 65, Madrid 28009, Spain
关键词
in vivo comet assay; ex vivo comet assay; DNA damage response; Drosophila melanogaster; NER; dmPolQ; mus308; mus201; mus308 and OK strains; MMS; NUCLEOTIDE EXCISION-REPAIR; METHYL METHANESULFONATE; MODEL CHEMICALS; ANIMAL-MODELS; GERM-CELLS; MELANOGASTER; MUS308; GENOTOXICITY; MUTATIONS; MUTAGENS;
D O I
10.3390/cells12151979
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The comet assay in Drosophila has been used in the last few years to study DNA damage responses (DDR) in different repair-mutant strains and to compare them to analyze DNA repair. We have used this approach to study interactions between DNA repair pathways in vivo. Additionally, we have implemented an ex vivo comet assay, in which nucleoids from treated and untreated cells were incubated ex vivo with cell-free protein extracts from individuals with distinct repair capacities. Four strains were used: wild-type OregonK (OK), nucleotide excision repair mutant mus201, dmPolQ protein mutant mus308, and the double mutant mus201;mus308. Methyl methanesulfonate (MMS) was used as a genotoxic agent. Both approaches were performed with neuroblasts from third-instar larvae; they detected the effects of the NER and dmPolQ pathways on the DDR to MMS and that they act additively in this response. Additionally, the ex vivo approach quantified that mus201, mus308, and the double mutant mus201;mus308 strains presented, respectively, 21.5%, 52.9%, and 14.8% of OK strain activity over MMS-induced damage. Considering the homology between mammals and Drosophila in repair pathways, the detected additive effect might be extrapolated even to humans, demonstrating that Drosophila might be an excellent model to study interactions between repair pathways.
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页数:12
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