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Investigation of micronucleus induction in MTH1 knockdown cells exposed to UVA, UVB or UVC
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
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Number of Authors: 5
2015 (English)In: Mutation research. Genetic toxicology and environmental mutagenesis, ISSN 1383-5718, E-ISSN 1879-3592, Vol. 793, no SI, 161-165 p.Article in journal (Refereed) Published
Abstract [en]

The longer wave parts of UVR can increase the production of reactive oxygen species (ROS) which can oxidize nucleotides in the DNA or in the nucleotide pool leading to mutations. Oxidized bases in the DNA are repaired mainly by the DNA base excision repair system and incorporation of oxidized nucleotides into newly synthesized DNA can be prevented by the enzyme MTH1. Here we hypothesize that the formation of several oxidized base damages (from pool and DNA) in close proximity, would cause a high number of base excision repair events, leading to DNA double strand breaks (DSB) and therefore giving rise to cytogenetic damage. If this hypothesis is true, cells with low levels of MTH1 will show higher cytogenetic damage after the longer wave parts of UVR. We analyzed micronuclei induction (MN) as an endpoint for cytogenetic damage in the human lymphoblastoid cell line, TK6, with a normal and a reduced level of MTH1 exposed to UVR. The results indicate a higher level of micronuclei at all incubation times after exposure to the longer wave parts of UVR. There is no significant difference between wildtype and MTH1-knockdown TK6 cells, indicating that MTH1 has no protective role in UVR-induced cytogenetic damage. This indicates that DSBs induced by UV arise from damage forms by direct interaction of UV or ROS with the DNA rather than through oxidation of dNTP.

Place, publisher, year, edition, pages
2015. Vol. 793, no SI, 161-165 p.
Keyword [en]
Ultraviolet radiation, MTH1, Micronucleus, Reactive oxygen species, Oxidative stress
National Category
Biochemistry and Molecular Biology Genetics Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:su:diva-125017DOI: 10.1016/j.mrgentox.2015.06.002ISI: 000364898400022PubMedID: 26520386OAI: oai:DiVA.org:su-125017DiVA: diva2:893284
Conference
11th International Symposium on Chromosomal Aberrations (ISCA), Rhodes, Greece, Sep 12-14, 2014
Available from: 2016-01-12 Created: 2016-01-07 Last updated: 2016-01-12Bibliographically approved

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Wojcik, AndrzejHaghdoost, Siamak
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Department of Molecular Biosciences, The Wenner-Gren Institute
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