ANALYSIS OF THE CD3 GENE REGION AND TYPE-1 DIABETES - APPLICATION OF FLUORESCENCE-BASED TECHNOLOGY TO LINKAGE DISEQUILIBRIUM MAPPING

Citation
Le. Pritchard et al., ANALYSIS OF THE CD3 GENE REGION AND TYPE-1 DIABETES - APPLICATION OF FLUORESCENCE-BASED TECHNOLOGY TO LINKAGE DISEQUILIBRIUM MAPPING, Human molecular genetics, 4(2), 1995, pp. 197-202
Citations number
40
Categorie Soggetti
Genetics & Heredity",Biology
Journal title
ISSN journal
09646906
Volume
4
Issue
2
Year of publication
1995
Pages
197 - 202
Database
ISI
SICI code
0964-6906(1995)4:2<197:AOTCGR>2.0.ZU;2-Q
Abstract
The CD3 gene region on chromosome 11q23 has been implicated in suscept ibility to type 1 (insulin-dependent) diabetes mellitus. Using semi-au tomated fluorescence-based technology, we have undertaken association and linkage analysis of a dinucleotide microsatellite in the CD3 delta (CD3D) gene. We have also performed a large case-control analysis of a restriction fragment length polymorphism (RFLP) in the CD3 epsilon ( CD3E) gene, 26 kb from CD3D. We found no evidence for the previously r eported association between the 8 kb allele of the RFLP and disease in a UK dataset of 403 diabetic patients and 446 nondiabetic controls. F urthermore, the use of the transmission/disequilibrium test (TDT) show ed no evidence of linkage or association to type 1 diabetes at either marker locus. We conclude that the CD3 gene region does not contribute significantly to IDDM susceptibility. We have successfully applied se mi-automated, fluorescence-based technology to undertake association a nalysis on the CD3D microsatellite. Moreover, by analysing 94 other di nucleotide repeat markers, we conclude that fluorescence-based methodo logy can generally be applied to large-scale, semi-automated associati on studies with most microsatellite markers.