A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Lee, Y., Paik, D., Bang, S., Kang, J., Chun, B., Lee, S., Bae, E., Chung, J., Kim, J. (2008). Loss of spastic paraplegia gene atlastin induces age-dependent death of dopaminergic neurons in Drosophila.  Neurobiol. Aging 29(1): 84--94. (Export to RIS)
FlyBase ID FBrf0202816
Publication Type Research paper
PubMed ID 17030474
PubMed Abstract Hereditary spastic paraplegias (HSPs) are human genetic disorders causing increased stiffness and overactive muscle reflexes in the lower extremities. atlastin (atl) is one of the major genes in which mutations result in HSP. We generated a Drosophila model of HSP that has a null mutation in atl. As they aged, atl null flies were paralyzed by mechanical shock such as bumping or vortexing. Furthermore, the flies showed age-dependent degeneration of dopaminergic neurons. These phenotypes were rescued by targeted expression of atl in dopaminergic neurons or feeding L-DOPA or SK&F 38393, an agonist of dopamine receptor. Our data raised the possibility that one of the causes of HSP disease symptoms in human patients with alt mutations is malfunction or degeneration of dopaminergic neurons.
DOI
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Supplementary material Appendix A. Supplementary data. [FBrf0209819]

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Secondary IDs FBrf0193044
Language of Publication English
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Publication Type Journal
Abbreviation Neurobiol. Aging
Title Neurobiology of Aging
Publication Year 1980-
ISBN/ISSN 0197-4580
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