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Metabolism of O6-alkyldeoxyguanosines and their effect on removal of O6-methylguanine from rat liver DNA.

作者信息

Pegg A E, Swann P F

出版信息

Biochim Biophys Acta. 1979 Dec 17;565(2):241-52. doi: 10.1016/0005-2787(79)90202-8.

DOI:10.1016/0005-2787(79)90202-8
PMID:518880
Abstract

O6-Methyldeoxyguanosine and O6-ethyldeoxyguanosine are weak inhibitors (of approximately equal potency) of the removal of O6-methylguanine from methylated DNA by a rat liver enzyme in vitro. When administered to rats, O6-ethyldeoxyguanosine retarded the removal from liver DNA of the O6-methylguanine which had been produced by pretreatment with dimethylnitrosamine, but the effect was short lived. O6-Methyldeoxyguanosine was much less effective. When cells in culture were grown in a medium containing radioactive O6-methylguanine or O6-methyldeoxyguanosine there was negligible incorporation of the methylated base into DNA, but substantial conversion to guanine which was incorporated. When these substances were injected into rats after partial hepatectomy, a very small incorporation of O6-methylguanine into DNA apparently occurred. Both O6-ethyldeoxyguanosine and O6-methyldeoxyguanosine were dealkylated by rat liver extracts, but the methylated derivative was metabolized much more rapidly. O6-Methylguanosine and O6-ethylguanosine were also dealkylated by rat liver extracts, but the corresponding bases were not attacked. This reaction was probably carried out by the adenosine deaminase in the extracts because it could be prevented by addition of erythro-9-(2-hydroxy-3-nonyl)adenine, a potent adenosine deaminase inhibitor, and could also be effected by purified calf intestinal adenosine deaminase. The Km for the demethylation of O6-methyldeoxyguanosine by calf intestinal adenosine deaminase was comparable to that for adenosine, whereas the Km for O6-ethyldeoxyguanosine was ten times greater. The V for O6-methyldeoxyguanosine was about 11% that for adenosine, but that for O6-ethyldeoxyguanosine was only 0.3%. The higher Km and the slower V for O6-ethyldeoxyguanosine may contribute to the slower dealkylation of this nucleoside by liver extracts and could account for its greater effect on slowing O6-methylguanine excision from DNA in vivo.

摘要

相似文献

1
Metabolism of O6-alkyldeoxyguanosines and their effect on removal of O6-methylguanine from rat liver DNA.
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2
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Arch Toxicol Suppl. 1980;3:55-68. doi: 10.1007/978-3-642-67389-4_5.

引用本文的文献

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Structure of -methyl-AMP deaminase ADAL with bound GMP and IMP and implications for -methyl-AMP recognition and processing.-甲基腺苷脱氨酶 ADAL 与 GMP 和 IMP 结合的结构及其对 -甲基-AMP 识别和加工的影响。
RNA Biol. 2019 Oct;16(10):1504-1512. doi: 10.1080/15476286.2019.1642712. Epub 2019 Jul 18.
2
Implication of localization of human DNA repair enzyme O6-methylguanine-DNA methyltransferase at active transcription sites in transcription-repair coupling of the mutagenic O6-methylguanine lesion.人类DNA修复酶O6-甲基鸟嘌呤-DNA甲基转移酶定位于活跃转录位点在诱变的O6-甲基鸟嘌呤损伤的转录-修复偶联中的意义。
Mol Cell Biol. 1998 Mar;18(3):1660-9. doi: 10.1128/MCB.18.3.1660.
3
The incorporation of O6-methyldeoxyguanosine and O4-methyldeoxythymidine monophosphates into DNA by DNA polymerases I and alpha.
DNA聚合酶I和α将O6-甲基脱氧鸟苷单磷酸和O4-甲基脱氧胸苷单磷酸掺入DNA中。
Nucleic Acids Res. 1983 Jun 25;11(12):4185-93. doi: 10.1093/nar/11.12.4185.
4
Increased cytotoxicity of 1-(2-chloroethyl)-1-nitroso-3(4-methyl)-cyclohexylurea by pretreatment with O6-methylguanine in resistant but not in sensitive human melanoma cells.在耐药而非敏感的人黑色素瘤细胞中,通过用O6-甲基鸟嘌呤预处理,1-(2-氯乙基)-1-亚硝基-3(4-甲基)-环己基脲的细胞毒性增加。
J Cancer Res Clin Oncol. 1987;113(4):387-91. doi: 10.1007/BF00397725.