Human p53 is a growth suppressor which not only functions in mammalian cell
s but also in fission yeast. It was previously shown that the cell cycle re
gulating phosphatase cdc25C suppresses the p53 induced growth arrest in fis
sion yeast. In the present study we analysed the mechanism of this suppress
ion. We found that cdc25C directly interacts with p53. By using different d
eletion mutants the binding region was narrowed down on the polypeptide cha
in of p53 to amino acids 287-340. To test the functional significance we an
alysed the effect of this interaction on the DNA binding activity of p53. A
s shown by band shift experiments binding of cdc25C to p53 does not modify
the DNA binding activity of p53. Our data suggest that the observed suppres
sion of the p53 induced growth arrest by cdc25C might be achieved by direct
binding of cdc25C to the C-terminus of p53.