| Literature DB >> 26093037 |
Jason R Kroll1, Arunesh Saras2, Mark A Tanouye3.
Abstract
This paper reviews Drosophila voltage-gated Na(+) channel mutations encoded by the para (paralytic) gene and their contributions to seizure disorders in the fly. Numerous mutations cause seizure-sensitivity, for example, para(bss1), with phenotypes that resemble human intractable epilepsy in some aspects. Seizure phenotypes are also seen with human GEFS+ spectrum mutations that have been knocked into the Drosophila para gene, para(GEFS+) and para(DS) alleles. Other para mutations, para(ST76) and para(JS) act as seizure-suppressor mutations reverting seizure phenotypes in other mutants. Seizure-like phenotypes are observed from mutations and other conditions that cause a persistent Na(+) current through either changes in mRNA splicing or protein structure.Entities:
Keywords: Drosophila; Epilepsy; Intractable epilepsy; Seizure-suppressor genes; Sodium channel
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Year: 2015 PMID: 26093037 PMCID: PMC4644469 DOI: 10.1016/j.expneurol.2015.06.018
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330