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
相关论文
共 100 条
[1]   POLYMORPHISM IN THE 5'-FLANKING REGION OF THE INSULIN GENE AND ITS POTENTIAL RELATION TO CARDIOVASCULAR-DISEASE RISK - OBSERVATIONS IN A BIRACIAL COMMUNITY - THE BOGALUSA HEART-STUDY [J].
AMOS, CI ;
COHEN, JC ;
SRINIVASAN, SR ;
FREEDMAN, DS ;
ELSTON, RC ;
BERENSON, GS .
ATHEROSCLEROSIS, 1989, 79 (01) :51-57
[2]   MAZ-DEPENDENT TERMINATION BETWEEN CLOSELY SPACED HUMAN-COMPLEMENT GENES [J].
ASHFIELD, R ;
PATEL, AJ ;
BOSSONE, SA ;
BROWN, H ;
CAMPBELL, RD ;
MARCU, KB ;
PROUDFOOT, NJ .
EMBO JOURNAL, 1994, 13 (23) :5656-5667
[3]   INSULIN GENE REGION-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES IS NOT RESTRICTED TO HLA-DR4-POSITIVE INDIVIDUALS [J].
BAIN, SC ;
PRINS, JB ;
HEARNE, CM ;
RODRIGUES, NR ;
ROWE, BR ;
PRITCHARD, LE ;
RITCHIE, RJ ;
HALL, JRS ;
UNDLIEN, DE ;
RONNINGEN, KS ;
DUNGER, DB ;
BARNETT, AH ;
TODD, JA .
NATURE GENETICS, 1992, 2 (03) :212-215
[4]   GAMETIC IMPRINTING IN MAMMALS [J].
BARLOW, DP .
SCIENCE, 1995, 270 (5242) :1610-1613
[5]   DIABETES IN IDENTICAL-TWINS - A STUDY OF 200 PAIRS [J].
BARNETT, AH ;
EFF, C ;
LESLIE, RDG ;
PYKE, DA .
DIABETOLOGIA, 1981, 20 (02) :87-93
[6]  
BELL GI, 1980, NATURE, V284, P26, DOI 10.1038/284026a0
[7]   THE HIGHLY POLYMORPHIC REGION NEAR THE HUMAN INSULIN GENE IS COMPOSED OF SIMPLE TANDEMLY REPEATING SEQUENCES [J].
BELL, GI ;
SELBY, MJ ;
RUTTER, WJ .
NATURE, 1982, 295 (5844) :31-35
[8]   A POLYMORPHIC LOCUS NEAR THE HUMAN INSULIN GENE IS ASSOCIATED WITH INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BELL, GI ;
HORITA, S ;
KARAM, JH .
DIABETES, 1984, 33 (02) :176-183
[9]   POLYMORPHIC DNA REGION ADJACENT TO THE 5'-END OF THE HUMAN INSULIN GENE [J].
BELL, GI ;
KARAM, JH ;
RUTTER, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09) :5759-5763
[10]   IDDM2-VNTR-encoded susceptibility to type 1 diabetes: Dominant protection and parental transmission of alleles of the insulin gene-linked minisatellite locus [J].
Bennett, ST ;
Wilson, AJ ;
Cucca, F ;
Nerup, J ;
Pociot, F ;
McKinney, PA ;
Barnett, AH ;
Bain, SC ;
Todd, JA .
JOURNAL OF AUTOIMMUNITY, 1996, 9 (03) :415-421