Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement

Hum Genet. 1992 May;89(3):353-6. doi: 10.1007/BF00220559.

Abstract

Mutations in the protein transthyretin cause amyloidosis involving the heart, peripheral nerves, and other organs. A family from West Virginia developed an unusually aggressive form of widespread transthyretin amyloidosis. Single-strand conformation polymorphism analysis revealed a variant in the transthyretin gene, which was found on sequencing to be a T----C transversion at position 2 of codon 55, corresponding to a Leu----Pro substitution. The variant sequence was confirmed by restriction analysis and polymerase chain reaction (PCR)-primer introduced restriction analysis.

Publication types

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

MeSH terms

  • Amyloidosis / genetics*
  • Base Sequence
  • Cardiomyopathies / genetics*
  • Cell Line, Transformed
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation / genetics
  • Nucleic Acid Conformation
  • Pedigree
  • Peripheral Nervous System Diseases / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length*
  • Prealbumin / genetics*
  • Proline / genetics

Substances

  • Prealbumin
  • Proline