Restriction fragment length polymorphism in the major histocompability complex of the non-obese diabetic mouse

Article


Lund, T., Simpson, E. and Cooke, A. 1990. Restriction fragment length polymorphism in the major histocompability complex of the non-obese diabetic mouse. Journal of Autoimmunity. 3 (3), pp. 289-298.
TypeArticle
TitleRestriction fragment length polymorphism in the major histocompability complex of the non-obese diabetic mouse
AuthorsLund, T., Simpson, E. and Cooke, A.
Abstract

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.

PublisherElsevier
JournalJournal of Autoimmunity
ISSN0896-8411
Publication dates
Print1990
Publication process dates
Deposited02 Feb 2010
Output statusPublished
Web address (URL)http://www.sciencedirect.com/science/article/pii/089684119090147K
LanguageEnglish
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