Primary structure of human amphiphysin, the dominant autoantigen of paraneoplastic stiff-man syndrome, and mapping of its gene (AMPH) to chromosome 7p13-p14

Hum Mol Genet. 1995 Feb;4(2):265-8. doi: 10.1093/hmg/4.2.265.

Abstract

Amphiphysin is a protein peripherally associated with synaptic vesicles. It is expressed in many neurons, certain endocrine cell types, and spermatocytes. Autoantibodies against amphiphysin occur in patients afflicted with a rare neurologic autoimmune disease, paraneoplastic Stiff-Man syndrome. To provide a basis for the understanding of anti-amphiphysin autoimmunity, we have cloned cDNAs and determined the primary structure of human amphiphysin. Comparison with chicken amphiphysin defines domains of low and high amino acid sequence conservation. As a candidate for heritable disorders of the nervous system, endocrine tissues or male fertility, the human amphiphysin gene was mapped to chromosome 7, region p13-p14.

Publication types

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

MeSH terms

  • Animals
  • Autoantigens / genetics
  • Base Sequence
  • Chickens
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 7*
  • Cloning, Molecular
  • Cricetinae
  • DNA, Complementary
  • Genes, Dominant
  • Humans
  • Molecular Sequence Data
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / immunology
  • Sequence Homology, Amino Acid
  • Stiff-Person Syndrome / genetics*

Substances

  • Autoantigens
  • DNA, Complementary
  • Nerve Tissue Proteins
  • amphiphysin

Associated data

  • GENBANK/X81438