mdm2 deletion does not alter growth characteristics of p53-deficient embryo fibroblasts

Kelly M. McMasters, Roberto Montes De Oca Luna, James R. Peña, Guillermina Lozano

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

The mdm2 gene encodes a protein that is necessary for the negative regulation of p53 function in vivo. Deletion of the mdm2 gene in mice results in early embryonic death while concomitant mdm2 and p53 deletion results in viable offspring. The viability of these mice prompted us to ask if MDM2 had an important growth regulatory function independent of p53. We established mouse embryo fibroblasts null for both p53 and mdm2 and compared them with p53-null fibroblasts. The cells did not differ in their growth rates or their ability to bypass a G1 arrest. Both cell lines formed colonies efficiently when plated at low density and showed a similar degree of genetic instability. Thus, the analysis of several growth parameters indicated no difference between p53-null and p53/mdm2-null cell lines.

Original languageEnglish (US)
Pages (from-to)1731-1736
Number of pages6
JournalOncogene
Volume13
Issue number8
StatePublished - 1996

Keywords

  • G arrest
  • Genomic instability
  • p53 null cells

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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