Open AccessGenetic and environmental interactions determine seizure susceptibility in epileptic EL mice
Author(s) -
Todorova M. T.,
Mantis J. G.,
Le M.,
Kim C. Y.,
Seyfried T. N.
Publication year - 2006
Publication title -
genes, brain and behavior
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.315
H-Index - 91
eISSN - 1601-183X
pISSN - 1601-1848
DOI - 10.1111/j.1601-183x.2006.00204.x
Subject(s) - quantitative trait locus , offspring , epilepsy , genetic architecture , biology , heritability , genetics , genetic predisposition , inheritance (genetic algorithm) , gene , neuroscience , pregnancy
Gene identification has progressed rapidly for monogenic epilepsies, but complex gene–environmental interactions have hindered progress in gene identification for multifactorial epilepsies. We analyzed the role of environmental risk factors in the inheritance of multifactorial idiopathic generalized epilepsy in the EL mouse. Seizure susceptibility was evaluated in the EL (E) and seizure‐resistant ABP/LeJ (A) parental mouse strains and in their AEF 1 and AEF 2 hybrid offspring using a handling‐induced seizure test. The seizure test was administered in three environments (environments I, II and III) that differed with respect to the number of seizure tests administered (one test or four tests) and the age of the mice when tested (young or old). The inheritance of seizure susceptibility appeared dominant after repetitive seizure testing in young or old mice, but recessive after a single test in old mice. Heritability was high (0.67–0.77) in each environment. Significant quantitative trait loci (QTL) that were associated with environments I and III (repetitive testing) were found on chromosomes 2 and 9 and colocalized with previously mapped El2 and El4 , respectively. The El2 QTL found in environment I associated only with female susceptibility. A novel QTL, El‐N , for age‐dependent predisposition to seizures was found on proximal chromosome 9 only in environment II. The findings indicate that environmental risk factors determine the genetic architecture of seizure susceptibility in EL mice and suggest that QTL for complex epilepsies should be defined in terms of the environment in which they are expressed.