Back to Search Start Over

Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33.

Authors :
Marron MP
Zeidler A
Raffel LJ
Eckenrode SE
Yang JJ
Hopkins DI
Garchon HJ
Jacob CO
Serrano-Rios M
Martinez Larrad MT
Park Y
Bach JF
Rotter JI
Yang MC
She JX
Source :
Diabetes [Diabetes] 2000 Mar; Vol. 49 (3), pp. 492-9.
Publication Year :
2000

Abstract

Polymorphic markers within the CTLA4 gene on chromosome 2q33 have been shown to be associated with type 1 diabetes. Therefore, a gene responsible for the disease (IDDM12) most likely lies within a region of <1-2 cM of CTLA4. To define more precisely the IDDM12 interval, we genotyped a multiethnic (U.S. Caucasian, Mexican-American, French, Spanish, Korean, and Chinese) collection of 178 simplex and 350 multiplex families for 10 polymorphic markers within a genomic interval of approximately 300 kb, which contains the candidate genes CTLA4 and CD28. The order of these markers (D2S346, CD28, GGAA19E07, D2S307, D2S72, CTLA4, D2S105, and GATA52A04) was determined by sequence tagged site content mapping of bacterial artificial chromosome (BAC) and yeast artificial chromosome (YAC) clones. The transmission disequilibrium test (TDT) analyses of our data revealed significant association/linkage with three markers within CTLA4 and two immediate flanking markers (D2S72 and D2S105) on each side of CTLA4 but not with more distant markers including the candidate gene CD28. Tsp analyses revealed significant association only with the three polymorphic markers within the CTLA4 gene. The markers linked and associated with type 1 diabetes are contained within a phagemid artificial chromosome clone of 100 kb, suggesting that the IDDM12 locus is either CTLA4 or an unknown gene in very close proximity.

Details

Language :
English
ISSN :
0012-1797
Volume :
49
Issue :
3
Database :
MEDLINE
Journal :
Diabetes
Publication Type :
Academic Journal
Accession number :
10868973
Full Text :
https://doi.org/10.2337/diabetes.49.3.492