DOI: 10.2337/db06-0402 © 2007 by the American Diabetes Association
Evaluation of Polymorphic Splicing in the Mechanism of the Association of the Insulin Gene With DiabetesFrom the Endocrine Genetics Laboratory, McGill University Health Center Research Institute, Montréal, Québec, Canada Address correspondence and reprint requests to Constantin Polychronakos, MD, McGill University Health Center, Montreal Childrens Hospital, 2300 Tupper St., Ste. C244, Montreal, Quebec, Canada H3H 1P3. E-mail: constantin.polychronakos{at}mcgill.ca
Abbreviations:
LD, linkage disequilibrium; SNP, single nucleotide polymorphism; UTR, untranslated region; VNTR, variable number of tandem repeats
The association of type 1 diabetes with the insulin gene (IDDM2 locus) has been mapped to a short haplotype encompassing two single nucleotide polymorphisms (SNPs) in perfect linkage disequilibrium (r2 = 1) with each other and with the two allele classes at the variable number of tandem repeats (VNTR) polymorphism upstream of the transcription site. Although it is believed that the genetic effect is mediated through transcriptional effects of the VNTR, an alternative mechanism has been recently proposed: In transfected cells, the common A allele at one of the SNPs (–23A
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