Enzymatic methylation of DNA and poly(dG-dC) X poly(dG-dC) modified by 4-acetoxyaminoquinoline-1-oxide, the ultimate carcinogen of 4-nitroquinoline-1-oxide |
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Authors: | A Pfohl-Leszkowicz S Galiegue-Zouitina B Bailleul M H Loucheux-Lefebvre G Dirheimer |
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Affiliation: | Department of Biochemistry, The University, Newcastle upon Tyne NE1 7RU, England |
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Abstract: | Both the initial velocity and the overall methylation of Ac-4HAQO modified DNA by a calf brain DNA (cytosine-5-)-methyltransferase are increased as compared to native DNA. The affinity of the modified DNA for the enzyme decreases as a function of the extent of the modification. Heat-denatured, single-stranded DNA shows exactly the opposite results: the more it is modified, the less it is methylated. The poly(dG-dC) X poly(dG-dC) modified by 4NQO is as well methylated as the non-modified one. The carcinogen may induce a tertiary structure favouring the 'walking' of the enzyme along the DNA. The hypermethylation caused by this carcinogen could have a significance in gene activity and cellular differentiation. |
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Keywords: | Branched-chain 2-oxoacid dehydrogenase complex Multi-site phosphorylation Mitochondria |
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