Spectrum of mutations induced by methyl and ethyl methanesulfonate at the hprt locus of normal and tag expressing Chinese hamster fibroblasts

Carcinogenesis. 1995 Jun;16(6):1281-5. doi: 10.1093/carcin/16.6.1281.

Abstract

This work describes the isolation and characterization of methyl methanesulfonate (MMS) and ethyl methanesulfonate (EMS) induced 6-thioguanine-resistant mutants in normal and Escherichia coli tag gene expressing Chinese hamster fibroblast, RJKO, cells. It was previously shown that increased removal of 3-alkylated adenine, effected by 3-methyladenine DNA glycosylase I (Tag), reduces the frequencies of hprt mutations induced by alkylating agents which produce mostly N-alkylation (MMS and EMS) to half the normal rate. In order to identify which type of mutation is suppressed by increased 3-alkyladenine repair we have determined the DNA base sequence changes of the hprt cDNA in 61 independent MMS- and EMS-induced mutant clones. For both cell types and irrespective of the agent used, the majority of mutations were GC to AT transitions originating in the non-transcribed strand. Only 6/55 base substitutions occurred at AT base pairs: five AT to GC transitions and one AT to CG transversion. Six mutations were found to be deletions. These results indicate that 3-alkylated adenines in DNA are not directly premutagenic. The fact that the mutation frequency is reduced by increased 3-alkyladenine removal might be explained by postulating the existence in mammalian cells of an SOS-like response turned on by cytotoxic lesions like 3-alkyladenine, or, alternatively, that increased removal of 3-alkyladenine increases the number of single-strand breaks in DNA, which stalls DNA replication and allows a prolonged time for DNA repair by the alkyltransferase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Animals
  • Base Sequence
  • Cell Line
  • Cricetinae
  • Cricetulus
  • DNA Glycosylases*
  • DNA Primers / chemistry
  • DNA Repair*
  • Ethyl Methanesulfonate / toxicity*
  • Hypoxanthine Phosphoribosyltransferase / genetics*
  • Methyl Methanesulfonate / toxicity*
  • Molecular Sequence Data
  • Mutagenesis / drug effects
  • N-Glycosyl Hydrolases / metabolism*
  • Thioguanine / pharmacology
  • Transfection

Substances

  • DNA Primers
  • Ethyl Methanesulfonate
  • Methyl Methanesulfonate
  • Hypoxanthine Phosphoribosyltransferase
  • 3-methyladenine-DNA glycosylase
  • DNA Glycosylases
  • N-Glycosyl Hydrolases
  • Thioguanine