Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat

Biochem J. 1994 Jul 1;301 ( Pt 1)(Pt 1):1-4. doi: 10.1042/bj3010001.

Abstract

Long-Evans Cinnamon rats develop a necrotizing hepatitis characterized by excessive hepatic copper accumulation, defective holoceruloplasmin biosynthesis and impaired biliary copper excretion. To elucidate the molecular basis of this defect, a cDNA clone encoding the rat Wilson disease gene was isolated and used to examine gene expression in selected tissues from normal and Long-Evans Cinnamon rats. Although this cDNA readily detects Wilson transcripts in liver and other tissues from normal rats, such transcripts are entirely absent from tissues derived from the Long-Evans Cinnamon rat strain. These data therefore identify the Long-Evans Cinnamon rat as the first bona fide animal model of Wilson disease and suggest that this rat strain may be a valuable resource in the study of this genetic disorder.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cation Transport Proteins*
  • Copper / metabolism
  • Copper-Transporting ATPases
  • DNA, Complementary / genetics
  • Gene Expression
  • Hepatolenticular Degeneration / genetics*
  • Hepatolenticular Degeneration / metabolism
  • Humans
  • Menkes Kinky Hair Syndrome / genetics
  • Menkes Kinky Hair Syndrome / metabolism
  • Molecular Sequence Data
  • Mutation
  • Rats
  • Rats, Mutant Strains
  • Sequence Homology, Amino Acid
  • Species Specificity

Substances

  • Cation Transport Proteins
  • DNA, Complementary
  • Copper
  • Adenosine Triphosphatases
  • Atp7a protein, rat
  • Copper-Transporting ATPases

Associated data

  • GENBANK/L28172
  • GENBANK/L28173