Repression of p53-dependent sequence-specific transactivation by MEF2c

Biochem Biophys Res Commun. 1995 Sep 14;214(2):468-74. doi: 10.1006/bbrc.1995.2310.

Abstract

Lambda ZAP cDNA library constructed from spleen of a p53-deficient mouse was screened by South-Western technique using Fragment A, a DNA sequence that p53 specifically binds to, as a probe. One (clone 2) of six clones isolated was identical to MEF2c, a MADS-family transcription factor. Transcripts of the mef2c gene was also detected in spleen where the expression has not been reported so far. Isolated clones except clone 2 had a growth-suppression activity on p53-deficient osteosarcoma cell line (Saos II). Clone 2 repressed the transactivation from Fragment A by p53, suggesting that MEF2c may act as a negative regulator of p53-responsive element.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Consensus Sequence
  • DNA, Complementary
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / metabolism*
  • Gene Expression
  • Gene Library
  • Genes, p53
  • Humans
  • Immunoblotting
  • MADS Domain Proteins
  • MEF2 Transcription Factors
  • Mice
  • Mice, Mutant Strains
  • Molecular Sequence Data
  • Myogenic Regulatory Factors*
  • Oligonucleotide Probes
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Spleen / metabolism
  • Transcription Factors / biosynthesis
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Transcriptional Activation*
  • Transfection
  • Tumor Suppressor Protein p53 / deficiency
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • MADS Domain Proteins
  • MEF2 Transcription Factors
  • MEF2C protein, human
  • Mef2c protein, mouse
  • Myogenic Regulatory Factors
  • Oligonucleotide Probes
  • Recombinant Proteins
  • Transcription Factors
  • Tumor Suppressor Protein p53