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Use of chromosome substitution strains to identify seizure susceptibility loci in mice.

Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Research Abstract Details 

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  • Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Abstract Text:

    melodie r winawerMelodie R Winawer,rachel kupermanRachel Kuperman,martin niethammerMartin Niethammer,steven shermanSteven Sherman,daniel rabinowitzDaniel Rabinowitz,irene plana guellIrene Plana Guell,christine a ponderChristine A Ponder,abraham a palmerAbraham A Palmer,

    Seizure susceptibility varies among inbred mouse strains. Chromosome substitution strains (CSS), in which a single chromosome from one inbred strain (donor) has been transferred onto a second strain (host) by repeated backcrossing, may be used to identify quantitative trait loci (QTLs) that contribute to seizure susceptibility. QTLs for susceptibility to pilocarpine-induced seizures, a model of temporal lobe epilepsy, have not been reported, and CSS have not previously been used to localize seizure susceptibility genes. We report QTLs identified using a B6 (host) x A/J (donor) CSS panel to localize genes involved in susceptibility to pilocarpine-induced seizures. Three hundred fifty-five adult male CSS mice, 58 B6, and 39 A/J were tested for susceptibility to pilocarpine-induced seizures. Highest stage reached and latency to each stage were recorded for all mice. B6 mice were resistant to seizures and slower to reach stages compared to A/J mice. The CSS for Chromosomes 10 and 18 progressed to the most severe stages, diverging dramatically from the B6 phenotype. Latencies to stages were also significantly shorter for CSS10 and CSS18 mice. CSS mapping suggests seizure susceptibility loci on mouse Chromosomes 10 and 18. This approach provides a framework for identifying potentially novel homologous candidate genes for human temporal lobe epilepsy.

    Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Publishing Authors By Initials

    mr winawerMR Winawer,r kupermanR Kuperman,m niethammerM Niethammer,s shermanS Sherman,d rabinowitzD Rabinowitz,ip guellIP Guell,ca ponderCA Ponder,aa palmerAA Palmer,

    For similar biological phenomena, cell phenomena, and immunity: immunity: antibody specificity: species specificity research abstracts see: biological phenomena, cell phenomena, and immunity: immunity: antibody specificity: species specificity research

    PUBMED ID PMID:

    MEDLINE DATE:

    Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Mammalian genome : official journal of the Interna

    VOLUME: 18

    Page Numbers: 23-31

    Journal Abbreviation: Mamm. Genome

    ISSN: 0938-8990

    DAY: 22

    MONTH: 01

    YEAR: 2007

    Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9100916

    Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Keywords Mesh Terms:

    KEYWORDS: Species Specificity

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Use of chromosome substitution strains to identify seizure susceptibility loci in mice. Information

    Substance Name: Pilocarpine

    Registry Number: 92-13-7

    Grant and Affiliation Information for Use of chromosome substitution strains to identify seizure susceptibility loci in mice.

    AFFILIATION: Department of Neurology, Columbia University, New York, NY 10032, USA. mw211@columbia.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIMH

    GRANT: MH70933

    ACRONYM: MH

    MEDLINETA: Mamm Genome

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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