Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat

Brain Res Mol Brain Res. 2002 May 30;101(1-2):132-5. doi: 10.1016/s0169-328x(02)00176-6.

Abstract

Deletions within the TOR1A gene cause early-onset (DYT1) torsion dystonia. We have cloned and sequenced the rat cDNA homologue of TOR1A and found a 91% identity with the human sequence. Northern blot analysis detects a single transcript of approximately 1.5 kb. In situ hybridization reveals a widespread distribution of torsinA mRNA within brain. No mutations were identified in the coding region of the gene in the genetically dystonic (dt) rat.

Publication types

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

MeSH terms

  • Animals
  • Brain / metabolism*
  • Brain / pathology
  • Brain / physiopathology
  • Carrier Proteins / genetics
  • Carrier Proteins / isolation & purification*
  • Cloning, Molecular
  • Disease Models, Animal
  • Dystonia Musculorum Deformans / genetics*
  • Dystonia Musculorum Deformans / metabolism
  • Dystonia Musculorum Deformans / physiopathology
  • Gene Expression / physiology*
  • Humans
  • Mice
  • Molecular Chaperones*
  • Molecular Sequence Data
  • Mutation / genetics
  • Neurons / metabolism*
  • Neurons / pathology
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Mutant Strains
  • Rats, Sprague-Dawley
  • Sequence Homology, Amino Acid
  • Sequence Homology, Nucleic Acid

Substances

  • Carrier Proteins
  • Dyt1 protein, mouse
  • Molecular Chaperones
  • RNA, Messenger
  • TOR1A protein, human
  • Tor1a protein, rat