The Wilms' tumor geneWt1is required for normal development of the retina

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Abstract
The Wilms' tumor gene Wt1 is known for its important functions during genitourinary and mesothelial formation. Here we show that Wt1 is necessary for neuronal development in the vertebrate retina. Mouse embryos with targeted disruption of Wt1 exhibit remarkably thinner retinas than age‐matched wild‐type animals. A large fraction of retinal ganglion cells is lost by apoptosis, and the growth of optic nerve fibers is severely disturbed. Strikingly, expression of the class IV POU‐domain transcription factor Pou4f2 (formerly Brn‐3b), which is critical for the survival of most retinal ganglion cells, is lost in Wt1−/− retinas. Forced expression of Wt1 in cultured cells causes an up‐regulation of Pou4f2 mRNA. Moreover, the Wt1(−KTS) splice variant can activate a reporter construct carrying 5′‐regulatory sequences of the human POU4F2 . The lack of Pou4f2 and the ocular defects in Wt1−/− embryos are rescued by transgenic expression of a 280 kb yeast artificial chromosome carrying the human WT1 gene. Taken together, our findings demonstrate a continuous requirement for Wt1 in normal retina formation with a critical role in Pou4f2‐dependent ganglion cell differentiation.