Human type 1 diabetes and the insulin gene: Principles of mapping polygenes

被引:232
作者
Bennett, ST
Todd, JA
机构
[1] Wellcome Trust Ctr. for Hum. Genet., Nuffield Department of Surgery, University of Oxford
基金
英国惠康基金;
关键词
multifactorial disease; human insulin gene; IDDM2; VNTR; minisatellite;
D O I
10.1146/annurev.genet.30.1.343
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We review the strategy used to identify a susceptibility locus (IDDM2) for type 1 (insulin dependent) diabetes mellitus. As type 1 diabetes is becoming the paradigm for dissecting multifactorial disease genetics, the approach described provides important general guidelines for positional cloning of human disease polygenes. Main topics include: (a) historical conspectus of the mapping and identification of IDDM2-a critical survey of the work leading up to the conclusion that IDDM2 most likely corresponds to allelic variation at the insulin gene minisatellite (VNTR) locus; (b) the nature of allelic (length and sequence) variation at the VNTR locus; (c) gene interactions and disease pathogenesis; (d) mechanism of action of the INS VNTR in type 1 diabetes-insulin gene expression, parent-of-origin effects (genomic imprinting); and (e) summary and future prospects-alleles of the insulin VNTR that are protective for type 1 diabetes appear to encode susceptibility to type 2 diabetes.
引用
收藏
页码:343 / 370
页数:28
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