Mapping by genetic interaction -: High-resolution congenic mapping of the type 1 diabetes loci Idd10 and Idd18 in the NOD mouse

被引:40
作者
Lyons, PA
Armitage, N
Lord, CJ
Phillips, MS
Todd, JA
Peterson, LB
Wicker, LS
机构
[1] Univ Cambridge, WT Diabet & Inflammat Lab, Juvenille Diabet Res Fdn, Cambridge CB2 2XY, England
[2] Merck Res Labs, Dept Human Genet, W Point, PA USA
[3] Merck Res Labs, Dept Pharmacol, Rahway, NJ USA
[4] Merck Res Labs, Dept Immunol, Rahway, NJ USA
[5] Merck Res Labs, Dept Rheumatol, Rahway, NJ USA
[6] Inst Canc Res, Chester Beatty Labs, London SW3 6JB, England
关键词
D O I
10.2337/diabetes.50.11.2633
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As many of the linked chromosome regions that predispose to type I diabetes in the NOD mouse have been dissected, it has become apparent that the initially observed effect is in fact attributable to several loci. One such cluster of loci on distal chromosome 3, originally described as Idd10, is now known to comprise three separate loci, Idd10, Idd17, and Idd18. Although these loci have a significant combined effect on diabetes development, their individual effects are barely detectable when diabetes is used as a read-out, which makes fine-mapping them by use of a conventional congenic approach impractical. In this study, we demonstrate that it is possible to map loci, with modest effects, to regions small enough for systematic gene identification by capitalizing on the fact that the combined loci provide more profound, measurable protection. We have mapped the Idd10 and Idd18 loci to 1.3- and 2.0-cM intervals, respectively, by holding the Idd3 allele constant. In addition, we have excluded Csf1 and Nras as candidates for both loci.
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收藏
页码:2633 / 2637
页数:5
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