Chemically induced mutations in mitochondrial DNA of human cells : Mutational spectrum of N-methyl-N'-nitro-N-nitrosoguanidine

• Published in: Cancer research (Chicago, Ill.) Vol. 58; no. 13; pp. 2857 - 2862
• Main Authors: MARCELINO, L. A, ANDRE, P. C, KHRAPKO, K, COLLER, H. A, GRIFFITH, J, THILLY, W. G
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 01.07.1998
• Subjects: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide - toxicity; Biological and medical sciences; Carcinogenesis, carcinogens and anticarcinogens; Cell Line; Chemical agents; DNA Mutational Analysis; DNA, Mitochondrial - drug effects; DNA, Mitochondrial - genetics; Humans; Hypoxanthine Phosphoribosyltransferase - drug effects; Hypoxanthine Phosphoribosyltransferase - genetics; Medical sciences; Methylnitronitrosoguanidine - toxicity; Mutagenesis - genetics; Mutagens - toxicity; Tumors; Human; Carcinogen; Mutagenesis; Lymphoproliferative syndrome; Acute; Established cell line; Malignant hemopathy; Mitochondrial DNA; Acute lymphocytic leukemia; Mutation; In vitro; Tumor cell
• ISSN: 0008-5472; 1538-7445

We have observed a reproducible mitochondrial mutational spectrum in the MT1 human lymphoblastoid line treated with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). The MNNG spectrum was distinct from the spontaneous mutational spectrum. However, our ability to observe MNNG-induced mitochondrial mutations above the high level of accumulated spontaneous mutations was dependent on the MT1 phenotype. MT1 cells are markedly resistant to the cytotoxicity but not the mutagenicity of MNNG, presumably as a result of inactivation of both copies of the hMSH6 (GTBP) mismatch repair gene. Thus, we were able to use conditions of treatment that yielded induced mitochondrial mutant fractions beyond the practical limits for human cell experiments in mismatch-proficient human cell lines. In contradistinction, when MT1 cells were treated repeatedly with maximum tolerated concentrations of (+/-) anti-benzo(a)pyrene diol-epoxide, no induced mitochondrial mutations above the spontaneous background were observed. A single dose of 4 microM MNNG (survival, 0.85) induced a mutant fraction of 8 x 10(-3) in the nuclear hypoxanthine-guanine phosphoribosyltrans. ferase gene, and a clear and reproducible pattern of seven MNNG-induced hotspot mutations was observed within the mitochondrial DNA target sequence studied (mitochondrial bp 10,030-10,130). All of the MNNG-induced hotspot mutations were G:C to A:T transitions present at frequencies between 6 x 10(-5) and 30 x 10(-5). Additional experiments supported the conclusion that MNNG-induced hotspot mutations observed were generated in living cells as a result of MNNG treatment and not from mismatch intermediates or DNA adducts converted into mutations during the PCR process.