RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS IN THE MAJOR HISTOCOMPATIBILITY COMPLEX OF THE NONOBESE DIABETIC MOUSE

被引:15
|
作者
LUND, T
SIMPSON, E
COOKE, A
机构
[1] UNIV COLL & MIDDLESEX SCH MED,MED MICROBIOL UNIT,LONDON W1P 9PG,ENGLAND
[2] CLIN RES CTR,TRANSPLANTAT BIOL SECT,HARROW HA1 3UJ,MIDDX,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0896-8411(90)90147-K
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inbred non-obese diabetic (NOD) mouse is a spontaneous model for insulin-dependent diabetes mellitus (IDDM). As in man and BB rats, IDDM in the NOD mouse has an autoimmune aetiology. The disease is controlled by several genes, one of which, Idd-1, has been mapped to the major histocompatibility complex (MHC) on chromosome 17. However, Idd-1 has not yet been identified. To facilitate the identification of Idd-1 we have further analysed the MHC region for restriction fragment length polymorphisms and we find that the NOD mouse has a distinct haplotype: H-2K1nod Kd Aβnod Aαd Eβnod Eαnod TNF-αb. In addition, the NOD mouse shows some similarities with the H-2b haplotype in the Q region, in that either the Q7 or the Q9 gene seems to be like that in the b-haplotype and that the Qa2 antigen is expressed, while other parts of this region are distinct from the b- as well as the d-haplotype. In contrast, the sister strain, the non-obese normal (NON) mouse, derived from the same cataract-prone line of mice as the NOD mouse, has an MHC Class I region indistinguishable from the b-haplotype, but the MHC Class II region is distinct from the NOD mouse as well as the b-, d- and k-haplotype. © 1990.
引用
收藏
页码:289 / 298
页数:10
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