mdm-2 Inhibits the G1 arrest and apoptosis functions of the p53 tumor suppressor protein

Jiandong Chen, Xiangwei Wu, Jiayuh Lin, Arnold J. Levine

Research output: Contribution to journalArticlepeer-review

336 Scopus citations

Abstract

The mdm-2 gene encodes a 90-kDa polypeptide that binds specifically to the p53 tumor suppressor protein. This physical interaction results in the inhibition of the transcriptional functions of p53 (J. Chen, J. Lin, and A. J. Levine, Mol. Med. 1:142-152, 1995, and J. Momand, G. P. Zambetti, D. C. Olson, D. George, and A. J. Levine, Cell 69:1237-1245, 1992). Experiments are described that demonstrate the ability of mdm-2 to abrogate both the p53- mediated cell cycle arrest and the apoptosis functions. In addition, the results presented here suggest that mdm-2 binding to p53 and the resultant inhibition of p53 transcription functions are critical for reversing p53- mediated cell cycle arrest. The N-terminal half or domain of the mdm-2 protein is sufficient to regulate these biological activities of p53, consistent with the possibility that the highly conserved central acidic region and the C-terminal putative zinc fingers of mdm-2 may encode other functions.

Original languageEnglish (US)
Pages (from-to)2445-2452
Number of pages8
JournalMolecular and cellular biology
Volume16
Issue number5
DOIs
StatePublished - May 1996
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Fingerprint

Dive into the research topics of 'mdm-2 Inhibits the G1 arrest and apoptosis functions of the p53 tumor suppressor protein'. Together they form a unique fingerprint.

Cite this