Rat kidney WT1 cDNAs contain either a thymidine or a cytosine residue
at position 839. Genomic WT1 DNA contains only T839. To explain these
results, we propose the WT1 transcript undergoes RNA editing in which
U839 is converted to C, resulting in the replacement of leucine 280 in
WT1 by proline. RNA editing at the same nucleotide was observed in WT
1 cDNAs from human testis. In functional assays, the WT1-leucine280 po
lypeptide repressed the EGR-1 promoter in in vitro assays approximatel
y 30% more efficiently than WT1-proline. Edited WT1-C839 mRNA was bare
ly detectable in neonatal kidney, whereas adult rat kidneys contained
both U839 and C839-WT1 mRNA, suggesting a role for the two protein iso
forms in growth and differentiation.