Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot

Charlotte A. Brown, Juergen Scharner, Kevin Felice, Matthew N. Meriggioli, Mark Tarnopolsky, Matthew Bower, Peter S. Zammit, Jerry R. Mendell, Juliet A. Ellis

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

Emery-Dreifuss muscular dystrophy (EDMD) is a neuromuscular disorder exhibiting a cardiomyopathy with cardiac conduction defects. X-linked EDMD arises from mutations in the EMD gene, which encodes for a nuclear membrane protein termed emerin. In this study, we describe novel and recurrent EMD mutations identified in 18 probands and three carriers from a cohort of 255 North American patients referred for EDMD genetic mutation analysis. Eight of these mutations are novel including six frameshift mutations (p.D9GfsX24, p.F39SfsX17, p.R45KfsX16, p.F190YfsX19, p.R203PfsX34 and p.R204PfsX7) and two non-sense mutations (p.S143X, p.W200X). Our data augment the number of EMD mutations by 13.8%, equating to an increase of 5.2% in the total known EMD mutations and to an increase of 6.0% in the number of different mutations. Analysis of the exon distribution of mutations within the EMD gene, suggests a nonrandom distribution, with exon 2 as a hot spot. This phenomenon may be due to its high GC content, which at 60% is the most GC-rich exon in the EMD gene. Journal of Human Genetics (2011) 56, 589-594; doi:10.1038/jhg.2011.65; published online 23 June 2011
Original languageEnglish
Pages (from-to)589 - 594
Number of pages6
JournalJournal of Human Genetics
Volume56
Issue number8
DOIs
Publication statusPublished - Aug 2011

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