Null mutation of PCLN-1/Claudin-16 results in bovine chronic interstitial nephritis

• Published in: Genome research 2000-05, Vol.10 (5), p.659-663
• Main Authors: Hirano, T, Kobayashi, N, Itoh, T, Takasuga, A, Nakamaru, T, Hirotsune, S, Sugimoto, Y
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Cattle; Chronic Disease; Genes, Recessive; Genetic Predisposition to Disease - etiology; Genetic Predisposition to Disease - genetics; Letter; Membrane Proteins - deficiency; Membrane Proteins - genetics; Microsatellite Repeats; Molecular Sequence Data; Nephritis, Interstitial - etiology; Nephritis, Interstitial - genetics; Sequence Deletion; Tight Junctions - genetics
• ISSN: 1088-9051; 1549-5469
• DOI: 10.1101/gr.10.5.659

Inherited chronic renal diseases are associated with failures in glomerular filtration and tubular resorption. Such failures invariably result from defects in selective filtration and absorption in surface renal epithelium. Recently, we described an autosomal recessive chronic interstitial nephritis with diffuse zonal fibrosis (CINF) in cattle. Bovine CINF, characterized by increased blood urea nitrogen, creatinine, and urinary proteins, leads to lethality before puberty, usually within the first 6 months or year of life. Here, we demonstrate that the first four exons of PCLN-1/Claudin-16 (CL-16), which encodes a member of the claudin family of tight junction proteins, were deleted in CINF-affected cattle. CL-16 was expressed preferentially in kidneys of normal cattle, but transcripts were totally absent in affected offspring. This observation suggests that the lack of CL-16 protein contributes to the dysfunction of paracellular renal transport systems.