Growth suppression induced by wild-type p53 protein is accompanied by selective down-regulation of proliferating-cell nuclear antigen expression

Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1958-62. doi: 10.1073/pnas.88.5.1958.

Abstract

The p53 gene is a frequent target of mutation in a wide variety of human cancers. Previously, it was reported that conditional expression of wild-type p53 protein in a cell line (GM47.23) derived from a human glioblastoma multiform tumor had a negative effect on cell proliferation. We have now investigated the effect that induction of wild-type p53 protein in this cell line has on the expression of the proliferating-cell nuclear antigen gene. The proliferating-cell nuclear antigen gene encodes a nuclear protein that is an auxiliary factor of DNA polymerase delta and part of the DNA replication machinery of the cell. We show that inhibition of cell cycle progression into S-phase after induction of wild-type p53 protein is accompanied by selective down-regulation of proliferating-cell nuclear antigen mRNA and protein expression.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, Neoplasm / genetics
  • Blotting, Northern
  • Cell Line
  • Fluorescent Antibody Technique
  • Humans
  • Nuclear Proteins / analysis
  • Nuclear Proteins / genetics
  • Plasmids
  • Proliferating Cell Nuclear Antigen
  • RNA / genetics
  • RNA / isolation & purification
  • RNA, Messenger / genetics
  • Restriction Mapping
  • Transfection
  • Tumor Suppressor Protein p53 / analysis
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Antigens, Neoplasm
  • Nuclear Proteins
  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger
  • Tumor Suppressor Protein p53
  • RNA