Logo image
eae36, a locus on mouse chromosome 4, controls susceptibility to experimental allergic encephalomyelitis in older mice and mice immunized in the winter
Journal article   Open access   Peer reviewed

eae36, a locus on mouse chromosome 4, controls susceptibility to experimental allergic encephalomyelitis in older mice and mice immunized in the winter

Cory Teuscher, R W Doerge, Parley D Fillmore and Elizabeth P Blankenhorn
Genetics (Austin), v 172(2), pp 1147-1153
Feb 2006
PMID: 16299394
url
https://doi.org/10.1534/genetics.105.049049View
Published, Version of Record (VoR) Open

Abstract

Genetic Predisposition to Disease - genetics Immunization Mice, Inbred C57BL Encephalomyelitis, Autoimmune, Experimental - immunology Genetic Markers Mice, Inbred Strains Animals Aging - genetics Encephalomyelitis, Autoimmune, Experimental - chemically induced Mice Polymorphism, Single Nucleotide Encephalomyelitis, Autoimmune, Experimental - genetics Seasons Microsatellite Repeats Crosses, Genetic
Genetic factors are believed to contribute to multiple sclerosis (MS) susceptibility; however, strong evidence implicating intrinsic and environmental factors in the etiopathogenesis of MS also exists. Susceptibility to experimental allergic encephalomyelitis (EAE), the principal animal model of MS, is also influenced by nongenetic factors, including age and season at immunization. This suggests that age- and season-by-gene interactions exist and that different susceptibility loci may influence disease as a function of the two parameters. In this study, linkage analysis based on genome exclusion mapping was carried out using age and season at immunization restricted cohorts of (B10.S x SJL/J) F2 intercross mice in an effort to identify such linkages. Significant linkage of EAE to eae4 and eae5 was detected with 6- to 12-week-old and summer cohorts. In contrast, significant linkage of EAE to eae4 and eae5 was not detected with the >12-week-old and winter/spring populations. Rather, significant linkage to D4Mit203 at 128.50 Mb on chromosome 4 was detected with animals that were >12 weeks old at the time of immunization or were immunized in the winter. This previously unidentified locus has been designated eae36. These results support the existence of age- and season-by-gene-specific interactions in the genetic control of susceptibility to autoimmune inflammatory disease of the central nervous system and suggest that late-onset MS may be immunogenetically distinct.

Metrics

7 Record Views
20 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Collaboration types
Domestic collaboration
Web of Science research areas
Genetics & Heredity
Logo image