A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis

Hum Genet. 1997 May;99(5):658-62. doi: 10.1007/s004390050424.

Abstract

A case of Duchenne muscular dystrophy is described with an unusual mutation consisting of a 17-bp deletion within exon 47 of the dystrophin gene. The sequences on either side of the deletion have a high degree of intrastrand base complementarity. It is hypothesised that the mechanism generating the deletion may have been the formation of hairpin loop structure in a single strand of DNA followed by enzymatic degradation at unpaired regions within the loop.

Publication types

  • Case Reports

MeSH terms

  • Algorithms
  • Base Sequence
  • Child, Preschool
  • DNA / chemistry
  • DNA / genetics
  • DNA Primers
  • Dystrophin / genetics*
  • Exons*
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Muscular Dystrophies / genetics*
  • Mutagenesis
  • Nucleic Acid Conformation
  • Pedigree
  • Phenotype
  • Polymerase Chain Reaction
  • Predictive Value of Tests
  • Sequence Deletion*

Substances

  • DNA Primers
  • Dystrophin
  • DNA