DUX4-Induced Histone Variants H3.X and H3.Y Mark DUX4 Target Genes for Expression
Rebecca Resnick,
Chao-Jen Wong,
Danielle C. Hamm,
Sean R. Bennett,
Peter J. Skene,
Sandra B. Hake,
Steven Henikoff,
Silvère M. van der Maarel,
Stephen J. Tapscott
Affiliations
Rebecca Resnick
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA; Medical Scientist Training Program, University of Washington, Seattle, WA 98195, USA
Chao-Jen Wong
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
Danielle C. Hamm
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
Sean R. Bennett
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
Peter J. Skene
NanoString Technologies, Seattle, WA 98109, USA
Sandra B. Hake
Institute for Genetics, Justus-Liebig-University Giessen, Hessen, Germany
Steven Henikoff
Basic Science Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA
Silvère M. van der Maarel
Department of Human Genetics, Leiden University Medical Center, 2333 Leiden, the Netherlands
Stephen J. Tapscott
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Corresponding author
Summary: The DUX4 transcription factor is briefly expressed in the early cleavage-stage embryo, where it induces an early wave of zygotic gene transcription, whereas its mis-expression in skeletal muscle causes the muscular dystrophy facioscapulohumeral dystrophy (FSHD). Here, we show that DUX4 induces the expression of the histone variants H3.X and H3.Y. We have used a myoblast cell line with doxycycline-inducible DUX4 to show that these histone variants are incorporated throughout the body of DUX4-induced genes. Following a brief pulse of DUX4, these histones contribute to greater perdurance and to enhanced re-activation of DUX4 target gene expression. These findings provide a model for H3.X/Y as a chromatin mechanism that facilitates the expression of DUX4 target genes subsequent to a brief pulse of DUX4 expression. : Resnick et al. show that the DUX4-induced histone variants, H3.X and H3.Y, incorporate into the chromatin of DUX4-induced genes, making them more sensitive to subsequent expression. This suggests a mechanism for how the brief expression of DUX4 can establish a memory of its transcriptional network. Keywords: DUX4, H3.X, H3.Y, facioscapulohumeral dystrophy, transcription, histone variants