The Wilms' tumor suppressor protein WT1 is a transcriptional regulator invo
lved in differentiation and the regulation of cell growth. WT1 is subject t
o alternative splicing, one isoform including a 17-amino acid region that i
s specific to mammals. The function of this 17-amino acid insertion is not
clear, however. Here, we describe a transcriptional activation domain in WT
1 that is specific to the WT1 splice isoform that contains the 17-amino aci
d insertion. We show that the function of this domain in transcriptional ac
tivation is dependent on a specific interaction with the prostate apoptosis
response factor par4. A mutation in WT1 found in Wilms' tumor disturbs the
interaction with par4 and disrupts the function of the activation domain.
Analysis of WT1 derivatives in cells treated to induce par4 expression show
ed a strong correlation between the transcription function of the WT1 17-am
ino acid insertion and the ability of WT1 to regulate cell survival and pro
liferation. Our results provide a molecular mechanism by which alternative
splicing of WT1 can regulate cell growth in development and disease.