Feline Polycystic Kidney Disease Mutation Identified in PKD1

Autosomal dominant polycystic kidney disease (AD- PKD) is a commonly inherited disorder in humans that causes the formation of fluid-filled renal cysts, often leading to renal failure. PKD1 mutations cause 85% of ADPKD. Feline PKD is autoso- mal dominant and has clinical presentations similar to humans. PKD affects ~38% of Persian cats worldwide, which is ~6% of cats, making it the most prominent inherited feline disease. Pre- vious analyses have shown significant linkage between the PKD phenotype and microsatellite markers linked to the feline homolog for PKD1. In this report, the feline PKD1 gene was scanned for causative mutations and a CA transversion was identified at c.10063 (human ref NM_000296) in exon 29, resulting in a stop mutation at position 3284, which suggests a loss of ~25% of the C-terminus of the protein. The same mutation has not been iden- tified in humans, although similar regions of the protein are truncated. The CA transversion has been identified in the het- erozygous state in 48 affected cats examined, including 41 Per- sians, a Siamese, and several other breeds that have been known to outcross with Persians. In addition, the mutation is segregating concordantly in all available PKD families. No unaffected cats have been identified with the mutation. No homozygous cats have been identified, supporting the suggestion that the mutation is embryonic lethal. These data suggest that the stop mutation causes feline PKD, providing a test to identify cats that will develop PKD and demonstrating that the domestic cat is an ideal model for human PKD.