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PMID: 15466259 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Feline polycystic kidney disease mutation identified in PKD1.

Journal of the American Society of Nephrology : JASN ·Vol. 15 ·No. 10 ·2004-10-00 ·Pages 2548-55

Lyons LA, Biller DS, Erdman CA, Lipinski MJ, Young AE, Roe BA, Qin B, Grahn RA

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) 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 autosomal dominant and has clinical presentations similar to humans. PKD affects approximately 38% of Persian cats worldwide, which is approximately 6% of cats, making it the most prominent inherited feline disease. Previous 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 C>A 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 approximately 25% of the C-terminus of the protein. The same mutation has not been identified in humans, although similar regions of the protein are truncated. The C>A transversion has been identified in the heterozygous state in 48 affected cats examined, including 41 Persians, 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.

MeSH Terms
Animals Base Sequence Cats Disease Models, Animal Female Gene Expression Regulation Genetic Predisposition to Disease Genotype Male Membrane Proteins/genetics Molecular Sequence Data Mutation Polycystic Kidney, Autosomal Dominant/genetics Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Proteins/genetics Reference Values Sensitivity and Specificity TRPP Cation Channels
Chemicals
Membrane Proteins Proteins TRPP Cation Channels polycystic kidney disease 1 protein
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lyons Leslie A
Department of Population Health & Reproduction, School of Veterinary Medicine, One Shields Avenue, University of California, Davis, 95616, USA. [email protected]
Biller David S
Erdman Carolyn A
Lipinski Monika J
Young Amy E
Roe Bruce A
Qin Baifang
Grahn Robert A
Article Info
Journal
Journal of the American Society of Nephrology : JASN
Abbr.
J Am Soc Nephrol
ISSN
1046-6673
Published
2004-10-00
Pages
2548-55
Language
English
Region
United States
NLM ID
9013836
Subset
IM
Grants
NHGRI NIH HHS · HG002153 · United States
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