Literature DB >> 708371

Formation and subsequent removal of O6-methylguanine from deoxyribonucleic acid in rat liver and kidney after small doses of dimethylnitrosamine.

A E Pegg, G Hui.   

Abstract

1. The amounts of 7-methylguanine and O(6)-methylguanine present in the DNA of liver and kidney of rats 4h and 24h after administration of low doses of dimethylnitrosamine were measured. 2. O(6)-Methylguanine was rapidly removed from liver DNA so that less than 15% of the expected amount (on the basis of 7-methylguanine found) was present within 4h after doses of 0.25mg/kg body wt. or less. Within 24h of administration of dimethylnitrosamine at doses of 1mg/kg or below, more than 85% of the expected amount of O(6)-methylguanine was removed. Removal was most efficient (defined in terms of the percentage of the O(6)-methylguanine formed that was subsequently lost within 24h) after doses of 0.25-0.5mg/kg body wt. At doses greater or less than this the removal was less efficient, even though the absolute amount of O(6)-methylguanine lost during 24h increased with the dose of dimethylnitrosamine over the entire range of doses from 0.001 to 20mg/kg body wt. 3. Alkylation of kidney DNA after intraperitoneal injections of 1-50mug of dimethylnitrosamine/kg body wt. occurred at about one-tenth the extent of alkylation of liver DNA. Removal of O(6)-methylguanine from the DNA also took place in the kidney, but was slower than in the liver. 4. After oral administration of these doses of dimethylnitrosamine, the alkylation of kidney DNA was much less than after intraperitoneal administration and represented only 1-2% of that found in the liver. 5. Alkylation of liver and kidney DNA was readily detectable when measured 24h after the final injection in rats that received daily injections of 1mug of [(3)H]dimethylnitrosamine/kg for 2 or 3 weeks. After 3 weeks, O(6)-methylguanine contents in the liver DNA were about 1% of the 7-methylguanine contents. The amount of 7-methylguanine in the liver DNA was 10 times that in the kidney DNA, but liver O(6)-methylguanine contents were only twice those in the kidney. 6. Extracts able to catalyse the removal of O(6)-methylguanine from alkylated DNA in vitro were isolated from liver and kidney. These extracts did not lead to the loss of 7-methylguanine from DNA. 7. The possible relevance of the formation and removal of O(6)-methylguanine in DNA to the risk of tumour induction by exposure to low concentrations of dimethylnitrosamine is discussed.

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Year:  1978        PMID: 708371      PMCID: PMC1185839          DOI: 10.1042/bj1730739

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  60 in total

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2.  Effect of a single treatment with the alkylating carcinogens dimethylnitrosamine, diethylnitrosamine and methyl methanesulphonate, on liver regenerating after partial hepatectomy. II. Alkylation of DNA and inhibition of DNA replication.

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Review 3.  Formation of N-nitroso compounds: chemistry, kinetics, and in vivo occurrence.

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5.  Purification and characterization of an endonuclease from calf thymus acting on irradiated DNA.

Authors:  S Bacchetti; R Benne
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Review 6.  Quantitative aspects of human exposure to nitrosamines.

Authors:  M C Archer; J S Wishnok
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Review 7.  Formation and metabolism of alkylated nucleosides: possible role in carcinogenesis by nitroso compounds and alkylating agents.

Authors:  A E Pegg
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8.  A new pathway for DNA repair in Escherichia coli.

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9.  Human endonuclease specific for apurinic/apyrimidinic sites in DNA. Partial purification and characterization of multiple forms from placenta.

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Journal:  J Biol Chem       Date:  1977-02-25       Impact factor: 5.157

10.  Effect of a single treatment with the alkylating carcinogens dimethylnitrosamine and methyl methanesulphonate on liver regenerating after partial hepatectomy. III. Effect on DNA synthesis in vivo and on DNA polymerase activity assayed in vitro.

Authors:  V M Craddock
Journal:  Chem Biol Interact       Date:  1976-11       Impact factor: 5.192

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  14 in total

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Review 2.  DNA glycosylases.

Authors:  S J Caradonna; Y C Cheng
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3.  Removal of O6-methylguanine from DNA by human liver fractions.

Authors:  A E Pegg; M Roberfroid; C von Bahr; R S Foote; S Mitra; H Bresil; A Likhachev; R Montesano
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4.  A system in mouse liver for the repair of O6-methylguanine lesions in methylated DNA.

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5.  Cell-specific differences in O6-alkylguanine DNA repair activity during continuous exposure to carcinogen.

Authors:  J A Swenberg; M A Bedell; K C Billings; D R Umbenhauer; A E Pegg
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

6.  O6-methylguanine repair in liver cells in vivo: comparison between G1- and S-phase of the cell cycle.

Authors:  H M Rabes; R Kerler; G Rode; C Schuster; R Wilhelm
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7.  Effect of partial hepatectomy on removal of O6-methylguanine from alkylated DNA by rat liver extracts.

Authors:  A E Pegg; W Perry; R A Bennett
Journal:  Biochem J       Date:  1981-07-01       Impact factor: 3.857

8.  Repair of O6-ethylguanine in DNA by a chromatin fraction from rat liver: transfer of the ethyl group to an acceptor protein.

Authors:  J R Mehta; D B Ludlum; A Renard; W G Verly
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

Review 9.  The formation and biological significance of N7-guanine adducts.

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10.  Excision of mutagenic replication-blocking lesions suppresses cancer but promotes cytotoxicity and lethality in nitrosamine-exposed mice.

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