Mutations of TP53 induce loss of DNA methylation and amplification of the TROP1 gene

Oncogene. 2003 Mar 20;22(11):1668-77. doi: 10.1038/sj.onc.1206248.

Abstract

p53 and DNA methylation play key roles in the maintenance of genome stability. In this work, we demonstrate that the two mechanisms are linked and that p53 plays a role in the maintenance of the DNA methylation levels. The loss of p53 was shown to induce loss of DNA methylation in the TROP1 gene, a human cancer-expressed locus that undergoes amplification when hypomethylated. This demethylation was reverted by the reintroduction of a wild-type TP53 (wtTP53) in the TP53-null cells. Using a gene-amplification assay in vivo, we demonstrate that the loss of p53 leads to a demethylation-dependent TROP1 gene amplification. The induction of gene amplification was reverted by the expression of a wtTP53 gene or by in vitro methylation of the transfected DNA with the Sss I DNA methylase. Taken together, these findings demonstrate that the inactivation of TP53 induces loss of DNA methylation and DNA methylation-dependent gene amplification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm / genetics*
  • Cell Adhesion Molecules / genetics*
  • Epithelial Cell Adhesion Molecule
  • Flow Cytometry
  • Gene Amplification*
  • Genes, p53*
  • Humans
  • Li-Fraumeni Syndrome / genetics
  • Mutation*
  • Transfection

Substances

  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule