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PLoS One. 2011;6(10):e26820. doi: 10.1371/journal.pone.0026820. Epub 2011 Oct 28.

The FSHD atrophic myotube phenotype is caused by DUX4 expression.

Author information

  • 1Laboratory of Molecular Biology, University of Mons, Mons, Belgium.

Abstract

BACKGROUND:

Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat array in which we identified the double homeobox 4 (DUX4) gene. We found stable DUX4 mRNAs only derived from the most distal D4Z4 unit and unexpectedly extended to the flanking pLAM region that provided an intron and a polyadenylation signal. DUX4 encodes a transcription factor expressed in FSHD but not control primary myoblasts or muscle biopsies. The DUX4 protein initiates a large transcription deregulation cascade leading to muscle atrophy and oxidative stress, which are FSHD key features.

METHODOLOGY/PRINCIPAL FINDINGS:

We now show that transfection of myoblasts with a DUX4 expression vector leads to atrophic myotube formation associated with the induction of E3 ubiquitin ligases (MuRF1 and Atrogin1/MAFbx) typical of muscle atrophy. DUX4 induces expression of downstream targets deregulated in FSHD such as mu-crystallin and TP53. We developed specific siRNAs and antisense oligonucleotides (AOs) targeting the DUX4 mRNA. Addition of these antisense agents to primary FSHD myoblast cultures suppressed DUX4 protein expression and affected expression of the above-mentioned markers.

CONCLUSIONS/SIGNIFICANCE:

These results constitute a proof of concept for the development of therapeutic approaches for FSHD targeting DUX4 expression.

PMID:
22053214
[PubMed - indexed for MEDLINE]
PMCID:
PMC3203905
Free PMC Article

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