Overexpression of oncoprotein MDM2 has been found in a significant number o
f human soft tissue tumors. In a subset of these tumors, overexpression is
a result of enhanced translation of mdm2 mRNA, There are two transcripts fr
om the mdm2 gene that differ only in their 5' leaders: a long form (L-mdm2)
and a short form (S-mdm2) that arise from the use of different promoters.
L-mdm2 mRNA contains two upstream open reading frames (uORFs) and this mRNA
was loaded with ribosomes inefficiently in comparison with S-mdm2, The 5'
leader of L-mdm2 was sufficient to transfer translational repression to a r
eporter gene and the two uORFs acted synergistically to achieve full suppre
ssion. In contrast, the 5' leader of S-mdm2 allowed efficient translation o
f an attached reporter gene in the tumor cells. These results are consisten
t with a model in which overexpression of MDM2 in certain tumors results fr
om a change in mRNA structure due to a switch in promoter usage.