Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis.
SourceAnnals of Neurology, 50, 6, (2001), pp. 816--9
Article / Letter to editor
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Annals of Neurology
SubjectEpidermal differentiation and cutaneous inflammation; Neuromuscular and neurometabolic disorders; Epidermale differentiatie en cutane ontstekingsprocessen; Neuromusculaire en neurometabole aandoeningen
Facioscapulohumeral muscular dystrophy is caused by partial deletion of the D4Z4 repeat array on chromosome 4q35. Genetic diagnosis is based on sizing of this repeat array, which is complicated by cross-hybridization of a homologous polymorphic repeat array on chromosome 10 and by the frequent exchanges between these chromosomal regions. The restriction enzyme XapI optimizes the diagnosis of facioscapulohumeral muscular dystrophy by uniquely digesting 4-derived repeat units and leaving 10-derived repeat units undigested, thus complementing BlnI, which uniquely digests 10-derived repeat units. A triple analysis with EcoRI, EcoRI/BlnI, and XapI unequivocally allows characterization of each of the four alleles, whether homogeneous or hybrid. This is particularly useful in the case of identical sized 4-derived and 10-derived arrays, in situations of suspected facioscapulohumeral muscular dystrophy with nonstandard allele configurations, and for assignment of hybrid fragments to their original alleles.
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