Localization of two insulin-dependent diabetes (Idd) genes to the Idd10 region on mouse Chromosome 3

被引:103
作者
Podolin, PL
Denny, P
Armitage, N
Lord, CJ
Hill, NJ
Levy, ER
Peterson, LB
Todd, JA
Wicker, LS
Lyons, PA
机构
[1] Merck Res Labs, Dept Autoimmune Dis Res, Rahway, NJ 07065 USA
[2] MRC, Mouse Genome Ctr, Harwell OX11 0RD, Oxon, England
[3] Univ Oxford, Nuffield Dept Surg, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[4] Univ Oxford, Mol Cytogenet Unit, Oxford OX3 7BN, England
[5] Merck Res Labs, Dept Pharmacol, Rahway, NJ 07065 USA
基金
英国惠康基金;
关键词
D O I
10.1007/s003359900749
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multiple genes control the development of autoimmune diabetes both in humans and in the nonobese diabetic (NOD) strain of mouse. Previously, three insulin-dependent diabetes (Idd) genes, Idd3, Idd10, and Idd17, were localized to mouse Chromosome (Chr) 3. The B10- or B6-derived resistance alleles at Idd10 and Idd3 together provide the NOD mouse with nearly complete protection from diabetes. In the present study, the 10.2-cM region encoding Idd10 was defined further with newly developed congenic strains. A locus, located in the centromeric 2.1 cM of the 10.2 cM region, contributed to the Idd10 trait. However, this locus did not account for the full effect of Idd10, suggesting the presence of a second gene in the distal portion of the 10.2-cM region. This second gene is designated as Idd18 and is localized to a 5.1-cM region. The resolution of the originally defined Idd3 locus into at least four separate loci, Idd3, Idd10, Idd17, and Idd18, illustrates the complex polygenic nature of diabetes.
引用
收藏
页码:283 / 286
页数:4
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