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PMID: 1871601 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genes for epilepsy mapped in the mouse.

Science (New York, N.Y.) ·Vol. 253 ·No. 5020 ·1991-08-09 ·Pages 669-73

Rise ML, Frankel WN, Coffin JM, Seyfried TN

Abstract

The neurological mutant mouse strain E1 is a model for complex partial seizures in humans. The inheritance of epileptic seizures with seven conventional chromosomal markers and over 60 endogenous proviral markers was studied by means of back-crosses of E1 with two seizure-resistant strains, DBA/2J and ABP/LeJ. The major gene responsible for this epileptic phenotype (El-1) was localized to a region distal with respect to the centromere on chromosome 9. At least one other gene, El-2, linked to proviral markers on chromosome 2, also influences the seizure phenotype. In addition, a potential modifier of seizures was detected in the DBA/2J background. The location of El-1 on distal chromosome 9 may allow identification of an epilepsy candidate gene in humans on the basis of conserved synteny with human chromosome 3.

MeSH Terms
Animals Chromosome Mapping Crosses, Genetic Epilepsy/genetics Female Genetic Predisposition to Disease Male Mice Mice, Inbred Strains Mice, Neurologic Mutants/genetics Recombination, Genetic Seizures/genetics Software
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rise M L
Department of Biology, Boston College, Chestnut Hill 02167.
Frankel W N
Coffin J M
Seyfried T N
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1991-08-09
Pages
669-73
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NINDS NIH HHS · NS 23355 · United States
NCI NIH HHS · R35CA44385 · United States
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