Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that is not due to a classical mutation within a protein-coding gene1,2. Instead, almost all FSHD patients carry deletions of an integral number of tandem 3.3-kilobase repeat units, termed D4Z4, located on chromosome 4q35 (ref. 3). D4Z4 contains a transcriptional silencer whose deletion leads to inappropriate overexpression in FSHD skeletal muscle of 4q35 genes located upstream of D4Z4 (ref. 4). To identify the gene responsible for FSHD pathogenesis, we generated transgenic mice selectively overexpressing in skeletal muscle the 4q35 genes FRG1, FRG2 or ANT1. We find that FRG1 transgenic mice develop a muscular dystrophy with features characteristic of the human disease; by contrast, FRG2 and ANT1 transgenic mice seem normal. FRG1 is a nuclear protein and several lines of evidence suggest it is involved in pre-messenger RNA splicing5,6,7. We find that in muscle of FRG1 transgenic mice and FSHD patients, specific pre-mRNAs undergo aberrant alternative splicing. Collectively, our results suggest that FSHD results from inappropriate overexpression of FRG1 in skeletal muscle, which leads to abnormal alternative splicing of specific pre-mRNAs.
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1 / D. Gabellini, G. D'Antona, M. Moggio, A. Prelle, C. Zecca, R. Adami, B. Angeletti, P. Ciscato, M.A. Pellegrino, R. Bottinelli, M.R. Green, R. Tupler. - In: NATURE. - ISSN 0028-0836. - 439:7079(2006 Feb 23), pp. 973-977.
|Titolo:||Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1|
D'ANTONA, GIUSEPPE (Secondo)
|Parole Chiave:||Muscular dystrophy model ; FRG1 ; Facioscapulohumeral muscular dystrophy|
|Data di pubblicazione:||23-feb-2006|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1038/nature04422|
|Appare nelle tipologie:||01 - Articolo su periodico|