The Drosophila slamdance Gene: A Mutation in an Aminopeptidase Can Cause Seizure, Paralysis and Neuronal Failure

Author:

Zhang HaiGuang1,Tan Jeff1,Reynolds Elaine2,Kuebler Daniel1,Faulhaber Sally1,Tanouye Mark13

Affiliation:

1. Department of Molecular and Cell Biology, Division of Neurobiology, University of California, Berkeley, California 94720

2. Department of Biology, Lafayette College, Easton, Pennsylvania 18042

3. Department of Environmental Science, Policy, and Management, Division of Insect Biology, University of California, Berkeley, California 94720

Abstract

Abstract We report here the characterization of slamdance (sda), a Drosophila melanogaster “bang-sensitive” (BS) paralytic mutant. This mutant exhibits hyperactive behavior and paralysis following a mechanical “bang” or electrical shock. Electrophysiological analyses have shown that this mutant is much more prone to seizure episodes than normal flies because it has a drastically lowered seizure threshold. Through genetic mapping, molecular cloning, and RNA interference, we have demonstrated that the sda phenotype can be attributed to a mutation in the Drosophila homolog of the human aminopeptidase N (APN) gene. Furthermore, using mRNA in situ hybridization and LacZ staining, we have found that the sda gene is expressed specifically in the central nervous system at particular developmental stages. Together, these results suggest that the bang sensitivity in sda mutants is caused by a defective APN gene that somehow increases seizure susceptibility. Finally, by using the sda mutation as a sensitized background, we have been able to identify a rich variety of sda enhancers and other independent BS mutations.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference64 articles.

1. Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice;Aigner;Cell,1995

2. Surface aminopeptidase activity of human lymphocytes. I. Biochemical and biologic properties of intact cells;Amoscato;J. Immunol.,1989

3. Knock-out mice reveal a critical antiepileptic role for neuropeptide Y;Barban;J. Neurosci.,1997

4. From the gene to behavior;Benzer;J. Am. Med. Assoc.,1971

5. Mutation of the Ca2+ channel β-subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse;Burgess;Cell,1997

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