Alkylation-induced apoptosis of embryonic stem cells in which the gene for DNA-repair, methyltransferase, had been disrupted by gene targeting

Yohei Tominaga, Teruhisa Tsuzuki, Akiko Shiraishi, Hisaya Kawate, Mutsuo Sekiguchi

Research output: Contribution to journalArticle

80 Citations (Scopus)

Abstract

An enzyme O6-methylguanine-DNA methyltransferase (MGMT) catalyzes transfer of a methyl group from O6-methylguanine and O4-methylthymine of alkylated DNA to its own molecule, thereby repairing the pre-mutagenic lesions in a single step reaction. Making use of gene targeting, we developed mouse embryonic stem (ES) cell lines deficient in the methyltransferase. Quantitative immunoblot analysis and enzyme assay revealed that MGMT(-/-)cells, in which both alleles were disrupted, contained no methyltransferase protein while cells with one intact allele (MGMT(+/-)) contained about half the amount of protein carried by the parental MGMT(+/+) cells. MGMT(-/-) cells have an extremely high degree of sensitivity to simple alkylating agents, N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) and N-methyl-N-nitrosourea (MNU), whereas MGMT(+/-) cells are slightly more sensitive to these agents, as compared with findings from normal cells. A high frequency of mutation was induced in MGM(-/-) cells on exposure to a relatively low dose of MNNG. Electrophoretic analyses of the DNAs as well as fluorochrome staining of the cells revealed that MGMT(-/-) cells treated with MNNG undergo apoptotic death, which occurs after G2-M arrest in the second cycle of cell proliferation.

Original languageEnglish
Pages (from-to)889-896
Number of pages8
JournalCarcinogenesis
Volume18
Issue number5
DOIs
Publication statusPublished - May 1 1997

All Science Journal Classification (ASJC) codes

  • Cancer Research

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