| Literature DB >> 24144844 |
Asal Fotouhi1, Winta Woldai Hagos, Marina Ilic, Andrzej Wojcik, Mats Harms-Ringdahl, Frank de Gruijl, Leon Mullenders, Jacob G Jansen, Siamak Haghdoost.
Abstract
Ultraviolet radiation is a highly mutagenic agent that damages the DNA by the formation of mutagenic photoproducts at dipyrimidine sites and by oxidative DNA damages via reactive oxygen species (ROS). ROS can also give rise to mutations via oxidation of dNTPs in the nucleotide pool, e.g. 8-oxo-dGTP and 2-OH-dATP and subsequent incorporation during DNA replication. Here we show that expression of human MutT homolog 1 (hMTH1) which sanitizes the nucleotide pool by dephosphorylating oxidized dNTPs, protects against mutagenesis induced by long wave UVA light and by UVB light but not by short wave UVC light. Mutational spectra analyses of UVA-induced mutations at the endogenous Thymidine kinase gene in human lymphoblastoid cells revealed that hMTH1 mainly protects cells from transitions at GC and AT base pairs.Entities:
Keywords: 2-OH-dA; 2-OH-dATP; 2-hydroxydeoxyadenosine; 2-hydroxydeoxyadenosine 5′-triphosphate; 6-4PP; 8-Oxo-dG; 8-oxo-2′-deoxyguanosine; 8-oxo-2′-deoxyguanosine-5′-triphosphate; 8-oxo-dG; 8-oxo-dGTP; CPD; KD; Nucleotide pool; Oxidative stress; ROS; TFT; TK6; Thymidine kinase; Tk; UVR; Ultraviolet radiation; WT; cyclobutane pyrimidine dimer; dNTP; deoxyribonucleotide triphosphate; hMTH1; human B lymphoblastoid cells; human MutT homolog protein; knockdown; pyrimidine (6-4) pyrimidone photoproduct; reactive oxygen species; trifluorothymidine; ultraviolet radiation; wildtype
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Year: 2013 PMID: 24144844 DOI: 10.1016/j.mrfmmm.2013.10.001
Source DB: PubMed Journal: Mutat Res ISSN: 0027-5107 Impact factor: 2.433