Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects

Hum Mol Genet. 2001 Oct 1;10(21):2385-96. doi: 10.1093/hmg/10.21.2385.

Abstract

A high level of polycystin-1 expression is detected in kidneys of all patients with autosomal dominant polycystic kidney disease (ADPKD). Mice that overexpress polycystin-1 also develop renal cysts. Whether overexpression of polycystin-1 is necessary for cyst formation is still unclear. Here, we report the generation of a targeted mouse mutant with a null mutation in Pkd1 and its phenotypic characterization in comparison with the del34 mutants that carry a 'truncation mutation' in Pkd1. We show that null homozygotes develop the same, but more aggressive, renal and pancreatic cystic disease as del34/del34. Moreover, we report that both homozygous mutants develop polyhydramnios, hydrops fetalis, spina bifida occulta and osteochondrodysplasia. Heterozygotes also develop adult-onset pancreatic disease. We show further that del34 homozygotes continue to produce mutant polycystin-1, thereby providing a possible explanation for increased immunoreactive polycystin-1 in ADPKD cyst epithelia in the context of the two-hit model. Our data demonstrate for the first time that loss of polycystin-1 leads to cyst formation and defective skeletogenesis, and indicate that polycystin-1 is critical in both epithelium and chondrocyte development.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bone Diseases / complications
  • Bone Diseases / genetics*
  • Disease Progression
  • Embryo, Mammalian / metabolism
  • Embryo, Mammalian / pathology
  • Female
  • Heterozygote
  • Homozygote
  • Hydrops Fetalis / complications
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Mice, Knockout
  • Mutation
  • Pancreatic Cyst / complications
  • Pancreatic Diseases / complications
  • Phenotype
  • Polycystic Kidney Diseases / complications
  • Polycystic Kidney Diseases / genetics*
  • Polyhydramnios / complications
  • Pregnancy
  • Proteins / genetics*
  • TRPP Cation Channels

Substances

  • Proteins
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein