Intergeneration CAG expansion and contraction in a Chinese HD family

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):242-4. doi: 10.1002/ajmg.b.30261.

Abstract

The prevalence of juvenile-onset Huntington's disease (HD) is about ten times lower than adult HD. Here we report a Chinese HD family showing both intergeneration CAG expansion and contraction. The expansion resulted from a paternal transmission which leads to juvenile-onset HD for a 17-year-old Chinese boy (III-5). More interestingly, a contraction was noticed in a maternal transmission (III-3), which changed the CAG repeat from an expanded, disease-causing allele (48 repeats) to a normal or intermediate allele (34 repeats). Of note, the contraction resulted in a deletion of 14 CAG repeats, which is much larger than previously reported contractions. Our results are consistent with previous observations in Western Caucasians that juvenile-onset HD is more likely inherited through the male germline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Alleles
  • China
  • Family Health
  • Female
  • Genotype
  • Humans
  • Huntingtin Protein
  • Huntington Disease / genetics*
  • Inheritance Patterns
  • Male
  • Middle Aged
  • Nerve Tissue Proteins / genetics*
  • Nuclear Proteins / genetics*
  • Pedigree
  • Polymorphism, Single Nucleotide
  • Sequence Analysis, DNA
  • Trinucleotide Repeat Expansion / genetics*
  • Trinucleotide Repeats / genetics*

Substances

  • HTT protein, human
  • Huntingtin Protein
  • Nerve Tissue Proteins
  • Nuclear Proteins

Associated data

  • OMIM/143100