A discrete region of the D4Z4 is sufficient to initiate epigenetic silencing

The DUX4 transcription factor is briefly expressed in the early embryo and is epigenetically repressed in somatic tissues. Loss of epigenetic repression can result in the aberrant expression of DUX4 in skeletal muscle and can cause facioscapulohumeral dystrophy (FSHD). Multiple factors have been identified as necessary to maintain epigenetic silencing of DUX4 in skeletal muscle, but whether specific sequences at the DUX4 locus are sufficient for initiating epigenetic silencing has not been known. We cloned fragments of the D4Z4 macrosatellite repeat, the DNA region that encompasses the DUX4 retrogene, adjacent to a reporter driven by a constitutive promoter and identified a single fragment sufficient to epigenetically repress reporter gene expression. Previously identified repressors of DUX4 expression-SETDB1, ATF7IP, SIN3A/B, and LRIF1-were necessary for silencing activity and p38 inhibitors enhanced suppression. These findings identify a key regulatory sequence for D4Z4 epigenetic repression and establish a model system for mechanistic and discovery studies.

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Publication Details

Journal
Human Molecular Genetics
Published
2025-06-27
DOI
https://doi.org/10.1093/hmg/ddaf114
Citations
1
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.81

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article

A discrete region of the D4Z4 is sufficient to initiate epigenetic silencing

Stephen J. Tapscott, Silvère M. van der Maarel, Taranjit S. Gujral, Frédéric Amant et al.
1 citations
Human Molecular Genetics
Muscle Physiology and Disorders
0.81
article

A discrete region of the D4Z4 is sufficient to initiate epigenetic silencing

Stephen J. Tapscott, Silvère M. van der Maarel, Taranjit S. Gujral, Frédéric Amant, Sean Bennett, Danielle C. Hamm, Ellen Paatela
article en
1 citations

Abstract

The DUX4 transcription factor is briefly expressed in the early embryo and is epigenetically repressed in somatic tissues. Loss of epigenetic repression can result in the aberrant expression of DUX4 in skeletal muscle and can cause facioscapulohumeral dystrophy (FSHD). Multiple factors have been identified as necessary to maintain epigenetic silencing of DUX4 in skeletal muscle, but whether specific sequences at the DUX4 locus are sufficient for initiating epigenetic silencing has not been known. We cloned fragments of the D4Z4 macrosatellite repeat, the DNA region that encompasses the DUX4 retrogene, adjacent to a reporter driven by a constitutive promoter and identified a single fragment sufficient to epigenetically repress reporter gene expression. Previously identified repressors of DUX4 expression-SETDB1, ATF7IP, SIN3A/B, and LRIF1-were necessary for silencing activity and p38 inhibitors enhanced suppression. These findings identify a key regulatory sequence for D4Z4 epigenetic repression and establish a model system for mechanistic and discovery studies.

Human Molecular GeneticsVol. 34(18)
Seattle Pacific University (US), Leiden University Medical Center (NL), Fred Hutch Cancer Center (US)
Fred Hutchinson Cancer Research Center, University of Washington, National Institutes of Health
Openalex Percentile: Top 26%
Muscle Physiology and Disorders
0.81
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A discrete region of the D4Z4 is sufficient to initiate epigenetic silencing — Stephen J. Tapscott, Silvère M. van der Maarel, et al. · Human Molecular Genetics (2025) | TGRS Research Map | TGRS