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Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation.

AbstractPURPOSE OF REVIEW:
In recent years, we have seen remarkable progress in our understanding of the disease mechanism underlying facioscapulohumeral muscular dystrophy (FSHD). The purpose of this review is to provide a comprehensive overview of our current understanding of the disease mechanism and to discuss the observations supporting the possibility of a developmental defect in this disorder.
RECENT FINDINGS:
In the majority of cases, FSHD is caused by contraction of the D4Z4 repeat array (FSHD1). This results in local chromatin relaxation and stable expression of the DUX4 retrogene in skeletal muscle, but only when a polymorphic DUX4 polyadenylation signal is present. In some cases (FSHD2), D4Z4 chromatin relaxation and stable DUX4 expression occur in the absence of D4Z4 array contraction. DUX4 is a germline transcription factor and its expression in skeletal muscle leads to activation of early stem cell and germline programs and transcriptional activation of retroelements.
SUMMARY:
Recent studies have provided a plausible disease mechanism for FSHD in which FSHD results from inappropriate expression of the germline transcription factor DUX4. The genes regulated by DUX4 suggest several mechanisms of muscle damage, and provide potential biomarkers and therapeutic targets that should be investigated in future studies.
AuthorsSilvère M van der Maarel, Daniel G Miller, Rabi Tawil, Galina N Filippova, Stephen J Tapscott
JournalCurrent opinion in neurology (Curr Opin Neurol) Vol. 25 Issue 5 Pg. 614-20 (Oct 2012) ISSN: 1473-6551 [Electronic] England
PMID22892954 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Chromatin
  • DUX4L1 protein, human
  • Homeodomain Proteins
Topics
  • Animals
  • Chromatin (pathology)
  • Homeodomain Proteins (genetics)
  • Humans
  • Muscle, Skeletal (metabolism, pathology)
  • Muscular Dystrophy, Facioscapulohumeral (genetics, pathology, physiopathology)
  • Transcription, Genetic

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