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Polycystic kidney disease 1 (PKD1) is the major locus of the common genetic disorder autosomal dominant polycystic kidney disease. We have studied PKD1 mRNA, with an RNase protection assay, and found widespread expression in adult tissue, with high levels in brain and moderate signal in kidney. Expression of the PKD1 protein, polycystin, was assessed in kidney using monoclonal antibodies to a recombinant protein containing the C terminus of the molecule. In fetal and adult kidney, staining is restricted to epithelial cells. Expression in the developing nephron is most prominent in mature tubules, with lesser staining in Bowman's capsule and the proximal ureteric bud. In the nephrogenic zone, detectable signal was observed in comma- and S-shaped bodies as well as the distal branches of the ureteric bud. By contrast, uninduced mesenchyme and glomerular tufts showed no staining. In later fetal (>20 weeks) and adult kidney, strong staining persists in cortical tubules with moderate staining detected in the loops of Henle and collecting ducts. These results suggest that polycystin's major role is in the maintenance of renal epithelial differentiation and organization from early fetal life. Interestingly, polycystin expression, monitored at the mRNA level and by immunohistochemistry, appears higher in cystic epithelia, indicating that the disease does not result from complete loss of the protein.

Type

Journal article

Journal

Proc Natl Acad Sci U S A

Publication Date

20/02/1996

Volume

93

Pages

1524 - 1528

Keywords

Adult, Animals, Antibodies, Monoclonal, Base Sequence, Epithelium, Gene Expression Regulation, Developmental, Humans, Immunoenzyme Techniques, Kidney, Mesoderm, Mice, Mice, Inbred BALB C, Molecular Sequence Data, Organ Specificity, Polycystic Kidney, Autosomal Dominant, Protein Biosynthesis, Proteins, RNA, Messenger, TRPP Cation Channels