Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/30158
Title: The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy
Authors: Martin, Melinda S.
Tang, Bin
Papale, Ligia Assumpção [UNIFESP]
Yu, Frank H.
Catterall, William A.
Escayg, Andrew
Emory Univ
Universidade Federal de São Paulo (UNIFESP)
Univ Washington
Issue Date: 1-Dec-2007
Publisher: Oxford Univ Press
Citation: Human Molecular Genetics. Oxford: Oxford Univ Press, v. 16, n. 23, p. 2892-2899, 2007.
Abstract: The mammalian genome contains four voltage-gated sodium channel genes that are primarily expressed in the central nervous system: SCN1A, SCN2A, SCN3A and SCN8A. Mutations in SCN1A and SCN2A are responsible for several dominant idiopathic epilepsy disorders, including generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy of infancy (SMEI). Mutations in SCN8A are associated with cognitive deficits and neuropsychiatric illness in humans and movement disorders in mice; however, a role for SCN8A (Na(v)1.6) in epilepsy has not been investigated. To determine the relationship between Nav1.6 dysfunction and seizure susceptibility, we examined the thresholds of two Scn8a mouse mutants, Scn8a(med) and Scn8a (med-jo), to flurothyl- and kainic acid (KA)-induced seizures. Both mutants were more seizure resistant than wild-type littermates, suggesting that altered Nav1.6 function reduces neuronal excitability. To determine whether impaired Nav1.6 function could ameliorate seizure severity in a mouse model of SMEI, we generated Scn1a(+/-); Scn8a (med-jo/+) double heterozygous mice. Unlike Scn1a(+/-) mice that are more susceptible to flurothyl- induced seizures, Scn1a(+/-); Scn8a(med-jo/+) mice displayed thresholds that were comparable to wildtype littermates. the Scn8a(med-jo) allele was also able to rescue the premature lethality of Scn1a(+/-) mice and extend the lifespan of Scn1a(-/-) mutants. These results demonstrate that genetic interactions can alter seizure severity and support the hypothesis that genetic modifiers contribute to the clinical variability observed in SMEI and GEFS+.
URI: http://repositorio.unifesp.br/handle/11600/30158
ISSN: 0964-6906
Other Identifiers: http://dx.doi.org/10.1093/hmg/ddm248
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