Localization of Idd11 using NOD congenic mouse strains:: elimination of Slc9a1 as a candidate gene
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Brodnicki, TC
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机构:Post Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
Brodnicki, TC
McClive, P
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机构:Post Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
McClive, P
Couper, S
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机构:Post Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
Couper, S
Morahan, G
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Post Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, AustraliaPost Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
Morahan, G
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[1] Post Off Royal Melbourne Hosp, Genet & Bioinformat Grp, Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[2] Cooperat Res Ctr Discovery Genes Common Human Dis, Melbourne, Vic, Australia
Type 1 diabetes is a multigenic autoimmune disease, the genetic basis for which is perhaps best characterized in the nonobese diabetic (NOD) mouse model. We previously located a NOD diabetes susceptibility locus, designated Idd11, on mouse Chromosome (Chr) 4 by analyzing diabetic backcross mice produced after crossing NOD/Lt with the nondiabetic resistant strain C57BL/6 (B6) strain. In order to confirm Idd11 and further refine its location, three NOD congenic mouse strains with different B6 derived intervals within Chr 4 were generated. Two of the congenic strains had a significant decrease in the cumulative incidence of diabetes compared with NOD/Lt control mice. The third NOD congenic strain, containing a B6 interval surrounding the Slc9a1 locus, was not protected against diabetes. These results define a new distal boundary for Idd11 and eliminate the Slc9a1 gene as a candidate. The Idd11 locus has now been definitively mapped to a 13cM interval on mouse Chr 4.