Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00427-003-0340-x
Title: Identification of the Drosophila melanogaster homolog of the human spastin gene
Authors: Kammermeier, L.
Spring, J.
Stierwald, M.
Burgunder, J.-M. 
Reichert, H.
Keywords: AAA domain
Drosophila melanogaster
Embryonic CNS
Spastin
Issue Date: 1-Aug-2003
Citation: Kammermeier, L., Spring, J., Stierwald, M., Burgunder, J.-M., Reichert, H. (2003-08-01). Identification of the Drosophila melanogaster homolog of the human spastin gene. Development Genes and Evolution 213 (8) : 412-415. ScholarBank@NUS Repository. https://doi.org/10.1007/s00427-003-0340-x
Abstract: The human SPG4 locus encodes the spastin gene, which is responsible for the most prevalent form of autosomal dominant hereditary spastic paraplegia (AD-HSP), a neurodegenerative disorder. Here we identify the predicted gene product CG5977 as the Drosophila homolog of the human spastin gene, with much higher sequence similarities than any other related AAA domain protein in the fly. Furthermore we report a new potential transmembrane domain in the N-terminus of the two homologous proteins. During embryogenesis, the expression pattern of Drosophila spastin becomes restricted primarily to the central nervous system, in contrast to the ubiquitous expression of the vertebrate spastin genes. Given this nervous system-specific expression, it will be important to determine if Drosophila spastin loss-of-function mutations also lead to neurodegeneration.
Source Title: Development Genes and Evolution
URI: http://scholarbank.nus.edu.sg/handle/10635/132536
ISSN: 0949944X
DOI: 10.1007/s00427-003-0340-x
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