A Long ncRNA Links Copy Number Variation to a Polycomb/Trithorax Epigenetic Switch in FSHD Muscular Dystrophy

• Published in: Cell Vol. 149; no. 4; pp. 819 - 831
• Main Authors: Cabianca, Daphne S., Casa, Valentina, Bodega, Beatrice, Xynos, Alexandros, Ginelli, Enrico, Tanaka, Yujiro, Gabellini, Davide
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 11.05.2012; Cell Press
• Subjects: Animals; Cells, Cultured; CHO Cells; chromatin; Chromatin remodeling; chromosome 4; copy number; Cricetinae; DNA-Binding Proteins - metabolism; Epigenesis, Genetic; epigenetics; gene expression; Gene mapping; genes; Genomes; Histone H3; Histone-Lysine N-Methyltransferase; histones; Humans; loci; Lysine; Methylation; Molecular Sequence Data; Muscle, Skeletal - metabolism; Muscle, Skeletal - pathology; Muscular dystrophy; Muscular Dystrophy, Facioscapulohumeral - genetics; Muscular Dystrophy, Facioscapulohumeral - physiopathology; Mutation; Myeloid-Lymphoid Leukemia Protein - metabolism; non-coding RNA; patients; Polycomb-Group Proteins; repetitive sequences; Repressor Proteins - metabolism; Repressors; Response Elements; RNA; RNA, Untranslated - metabolism; Transcription; transcription (genetics); Transcription Factors - metabolism
• ISSN: 0092-8674; 1097-4172; 1097-4172
• DOI: 10.1016/j.cell.2012.03.035

Repetitive sequences account for more than 50% of the human genome. Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant disease associated with reduction in the copy number of the D4Z4 repeat mapping to 4q35. By an unknown mechanism, D4Z4 deletion causes an epigenetic switch leading to de-repression of 4q35 genes. Here we show that the Polycomb group of epigenetic repressors targets D4Z4 in healthy subjects and that D4Z4 deletion is associated with reduced Polycomb silencing in FSHD patients. We identify DBE-T, a chromatin-associated noncoding RNA produced selectively in FSHD patients that coordinates de-repression of 4q35 genes. DBE-T recruits the Trithorax group protein Ash1L to the FSHD locus, driving histone H3 lysine 36 dimethylation, chromatin remodeling, and 4q35 gene transcription. This study provides insights into the biological function of repetitive sequences in regulating gene expression and shows how mutations of such elements can influence the progression of a human genetic disease. [Display omitted] ► In healthy subjects, the FSHD locus is a Polycomb repressive target ► FSHD patients display loss of Polycomb silencing and gain of Trithorax activation ► DBE-T is a chromatin-bound ncRNA expressed selectively in FSHD patients ► DBE-T recruits Ash1L to the FSHD locus to coordinate long-range gene de-repression Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal-dominant myopathy associated with a reduced number of D4Z4 repeats, which leads to the expression of a noncoding RNA in a nearby locus. This RNA recruits a Trithorax epigenetic activator, which then switches on the transcription of genes driving FSHD.