A novel mutation in the spastin gene in a family with spastic paraplegia

Neurosci Lett. 2002 May 31;325(1):57-61. doi: 10.1016/s0304-3940(02)00239-2.

Abstract

Hereditary spastic paraplegia (HSP) is a degenerative neuromuscular disease characterized by progressive lower extremity weakness, spasticity and hyperreflexia. Inheritance of HSP is commonly autosomal dominant, spastin was identified as the defective gene in chromosome 2p-linked autosomal dominant hereditary spastic paraplegia (AD-HSP). In a large American family with AD-HSP, we have identified a novel spastin mutation at a splice-acceptor site in intron 6 (1130-1 g--> a) and detected a corresponding aberrant transcript generated from a cryptic splice site. This is predicted to cause a frameshift and premature truncation of the abnormal spastin protein. Our data are the first to confirm that a mutation in an acceptor site in the spastin gene results in activation of a cryptic acceptor site and a translational frameshift. The clinical phenotype of this pedigree is also discussed.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Amino Acid Sequence / genetics
  • Base Sequence / genetics
  • Calcium-Binding Proteins / genetics*
  • Chromosomes, Human, Pair 2 / genetics
  • Female
  • Frameshift Mutation* / genetics
  • Genetic Linkage
  • Heterozygote
  • Humans
  • Introns
  • Male
  • Molecular Sequence Data
  • Paraplegia / genetics*
  • Pedigree
  • RNA Splice Sites
  • Spastin

Substances

  • Calcium-Binding Proteins
  • RNA Splice Sites
  • Adenosine Triphosphatases
  • Spastin
  • SPAST protein, human