Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis. Issue 10 (1st October 2000)

• Record Type: Journal Article
• Authors: Lindsey, J C; Lusher, M E; McDermott, C J; White, K D; Reid, E; Rubinsztein, D C; Bashir, R; Hazan, J; Shaw, P J; Bushby, K M D
• Is Part Of: Journal of medical genetics. Volume 37:Issue 10(2000)
• Page Start: 759
• Page End: 765
• Publication Date: 2000-10-01
• Subjects: spastin -- hereditary spastic paraparesis -- mutation -- recessive; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.37.10.759
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : BACKGROUND: Hereditary spastic paraparesis is a genetically heterogeneous condition. Recently, mutations in the spastin gene were reported in families linked to the common SPG4 locus on chromosome 2p21-22. OBJECTIVES: To study a population of patients with hereditary spastic paraparesis for mutations in the spastin gene ( SPG4 ) on chromosome 2p21-22. METHODS: DNA from 32 patients (12 from families known to be linked to SPG4 ) was analysed for mutations in the spastin gene by single strand conformational polymorphism analysis and sequencing. All patients were also examined clinically. RESULTS: Thirteen SPG4 mutations were identified, 11 of which are novel. These mutations include missense, nonsense, frameshift, and splice site mutations, the majority of which affect the AAA cassette. We also describe a nucleotide substitution outside this conserved region which appears to behave as a recessive mutation. CONCLUSIONS: Recurrent mutations in the spastin gene are uncommon. This reduces the ease of mutation detection as a part of the diagnostic work up of patients with hereditary spastic paraparesis. Our findings have important implications for the presumed function of spastin and schemes for mutation detection in HSP patients.