Chromosome Research

, Volume 2, Issue 3, pp 225–234

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease

  • Sara T. Winokur
  • Ulla Bengtsson
  • Julie Feddersen
  • Kathy D. Mathews
  • Barbara Weiffenbach
  • Holly Bailey
  • Rachelle P. Markovich
  • Jeffrey C. Murray
  • John J. Wasmuth
  • Michael R. Altherr
  • Brian C. Schutte
Article

DOI: 10.1007/BF01553323

Cite this article as:
Winokur, S.T., Bengtsson, U., Feddersen, J. et al. Chromosome Res (1994) 2: 225. doi:10.1007/BF01553323

Abstract

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant form of muscular dystrophy. The FSHD locus has been linked to the most distal genetic markers on the long arm of chromosome 4. Recently, a probe was identified that detects anEcoRI fragment length polymorphism which segregates with the disease in most FSHD families. Within theEcoRI fragment lies a tandem array of 3.2 kb repeats. In several familial cases and four independent sporadic FSHD mutations, the variation in size of theEcoRI fragment was due to a decrease in copy number of the 3.2 kb repeats. To gain further insight into the relationship between the tandem array and FSHD, a single 3.2 kb repeat unit was characterized. Fluorescencein situ hybridization (FISH) demonstrates that the 3.2 kb repeat cross-hybridizes to several regions of heterochromatin in the human genome. In addition, DNA sequence analysis of the repeat reveals a region which is highly homologous to a previously identified family of heterochromatic repeats, LSau. FISH on interphase chromosomes demonstrates that the tandem array of 3.2 kb repeats lies within 215 kb of the 4q telomere. Together, these results suggest that the tandem array of 3.2 kb repeats, tightly linked to the FSHD locus, is contained in heterochromatin adjacent to the telomere. In addition, they are consistent with the hypothesis that the gene responsible for FSHD may be subjected to position effect variegation because of its proximity to telomeric heterochromatin.

Key words

heterochromatintelomererepetitive DNA familyfacioscapulohumeral muscular dystrophyposition effect variegation

Copyright information

© Rapid Communications of Oxford Ltd 1994

Authors and Affiliations

  • Sara T. Winokur
    • 1
  • Ulla Bengtsson
    • 1
  • Julie Feddersen
    • 2
  • Kathy D. Mathews
    • 2
  • Barbara Weiffenbach
    • 3
  • Holly Bailey
    • 2
  • Rachelle P. Markovich
    • 1
  • Jeffrey C. Murray
    • 2
  • John J. Wasmuth
    • 1
  • Michael R. Altherr
    • 1
    • 4
  • Brian C. Schutte
    • 2
  1. 1.Department of Biological ChemistryUniversity of CaliforniaIrvineUSA
  2. 2.Department of PediatricsUniversity of Iowa Hospitals and ClinicsIowa CityUSA
  3. 3.Collaborative Research Inc.WalthamUSA
  4. 4.Genomics and Structural Biology GroupLANLLos AlamosUSA