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Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3)
Authors:Andrea H Nmeth  Dagmar Nolte  Eimear Dunne  Stephan Niemann  Markus Kostrzewa  Usha Peters  Eileen Fraser  Elena Bochukova  Robin Butler  Julie Brown  Roger D Cox  Elaine R Levy  Hans-Hilger Ropers  Anthony P Monaco  Ulrich Müller
Institution:Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford, OX3 7BN, England. hilary.nemeth@well.ox.ac.uk
Abstract:X-linked dystonia-parkinsonism (XDP) is a recessive disorder characterized by generalized dystonia with some patients exhibiting parkinsonism. The disease gene, DYT3, is located between DXS453 (DXS993) and DXS559, and strongest linkage disequilibrium is found distal to DXS7117 and proximal to DXS559. We have isolated and analyzed four novel polymorphic markers between DXS7117 and DXS559 and, by haplotype analysis, have narrowed the candidate interval to <350 kb. A sequence-ready contig of 700 kb has been constructed spanning DXS7117 to DXS559 and is composed of 35 PACs, BACs, and cosmids. Nine genes and novel ESTs have been mapped into this contig, and mutations in the coding regions and intron-exon borders of two genes have been excluded as the cause of XDP. Several of the other genes and ESTs located within the contig code for proteins implicated in normal brain development and function and are candidates for DYT3.
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