Genomic differences between O6-methylguanine-DNA methyltransferase proficient (Mex+) and deficient (Mex-) cell lines: possible role of genetic and epigenetic changes in conversion of Mex+ into Mex-

Biochem Biophys Res Commun. 1992 Mar 31;183(3):1184-90. doi: 10.1016/s0006-291x(05)80315-8.

Abstract

Cell lines that possess O6-methylguanine-DNA methyltransferase (MGMT) repair activity (Mex+ phenotype) or are deficient for MGMT (Mex-) are compared at genomic level. It is shown that 1) 208F rat cells do not contain the MGMT gene, as detected by Southern blot hybridization. 2) Mex- HeLa MR and CHO-9 cells express very low amounts of MGMT mRNA, as detected by PCR. The size of the MGMT specific PCR product was slightly smaller than that generated from Mex+ HeLa S3 cells. 3) HeLa MR, compared to various human Mex+ cell lines, shows a restriction fragment length polymorphism indicating mutational alteration of MGMT gene sequences. 4) Mex- cells (HeLa MR) and cells that express very low MGMT activity (GM637) exhibit hypomethylation of the MGMT gene as revealed by MspI/HpaII restriction digests. 5) Exposure of Mex- cells to 5-azacytidine and selection with N-hydroxyethyl-N-chloroethylnitrosourea (HeCNU) did not yield Mex+ revertants. With V79 cells treated with 5-azacytidine clones resistant to HeCNU were isolated. These cells were MGMT deficient and not cross-resistant to N-methyl-N'-nitro-N-nitrosoguanidine indicating the existance of a defence mechanism other than MGMT against chloroethylating agents. The data suggest down-regulation of MGMT transcription accompanied by decreasing CpG methylation, but in some cell lines also mutational alterations to be involved in extinction of the Mex+ phenotype.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Survival
  • HeLa Cells / drug effects
  • Humans
  • Methylnitronitrosoguanidine / pharmacology
  • Methyltransferases / deficiency
  • Methyltransferases / genetics*
  • Methyltransferases / metabolism
  • Mutagenesis
  • Mutagens / pharmacology
  • Mutation / genetics*
  • Nitrosourea Compounds / pharmacology
  • O(6)-Methylguanine-DNA Methyltransferase
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • RNA Precursors
  • Rats

Substances

  • Mutagens
  • Nitrosourea Compounds
  • RNA Precursors
  • Methylnitronitrosoguanidine
  • Methyltransferases
  • O(6)-Methylguanine-DNA Methyltransferase
  • elmustine