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果蝇的“狂舞”基因:一种氨肽酶的突变可导致癫痫、麻痹和神经元功能衰竭。

The Drosophila slamdance gene: a mutation in an aminopeptidase can cause seizure, paralysis and neuronal failure.

作者信息

Zhang HaiGuang, Tan Jeff, Reynolds Elaine, Kuebler Daniel, Faulhaber Sally, Tanouye Mark

机构信息

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

出版信息

Genetics. 2002 Nov;162(3):1283-99. doi: 10.1093/genetics/162.3.1283.

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.

摘要

我们在此报告对“霹雳舞”(sda)的特征描述,它是黑腹果蝇的一种“对敲击敏感”(BS)的麻痹突变体。该突变体在受到机械“敲击”或电击后会表现出多动行为和麻痹。电生理分析表明,此突变体比正常果蝇更容易发生癫痫发作,因为它的癫痫阈值大幅降低。通过基因定位、分子克隆和RNA干扰,我们已经证明sda表型可归因于人类氨肽酶N(APN)基因在果蝇中的同源基因突变。此外,利用mRNA原位杂交和LacZ染色,我们发现sda基因在特定发育阶段在中枢神经系统中特异性表达。这些结果共同表明,sda突变体中的敲击敏感性是由有缺陷的APN基因引起的,该基因以某种方式增加了癫痫易感性。最后,通过将sda突变作为敏感背景,我们已经能够鉴定出丰富多样的sda增强子和其他独立的BS突变。

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