IDDM2-VNTR-encoded susceptibility to type 1 diabetes: Dominant protection and parental transmission of alleles of the insulin gene-linked minisatellite locus

被引:137
作者
Bennett, ST
Wilson, AJ
Cucca, F
Nerup, J
Pociot, F
McKinney, PA
Barnett, AH
Bain, SC
Todd, JA
机构
[1] UNIV LEEDS,RES SCH MED,PAEDIAT EPIDEMIOL GRP,LEEDS LS2 9LN,W YORKSHIRE,ENGLAND
[2] STENO DIABET CTR,DK-2820 GENTOFTE,DENMARK
[3] UNIV BIRMINGHAM,BIRMINGHAM HEARTLANDS HOSP,DEPT MED DIABET ENDOCRINOL,BIRMINGHAM B9 5SS,W MIDLANDS,ENGLAND
基金
英国惠康基金;
关键词
insulin gene expression; genomic imprinting; IDDM2;
D O I
10.1006/jaut.1996.0057
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IDDM2-encoded predisposition to type 1 diabetes has recently been mapped to the minisatellite or variable number of tandem repeat (VNTR) locus upstream of the insulin and insulin-like growth factor II genes on human chromosome 11p15.5. In a UK case-control study (n=228 sporadic diabetics; n=441 healthy controls), we show here that the genotype homozygous for VNTR class I alleles is predisposing to disease (RR=2.68), and VNTR class III alleles are dominantly protective (RR=0.37). In 722 diabetic families from the UK (n=356), USA (n=173), Denmark (n=55) and Sardinia (n=138), we have analysed the transmission of class I alleles to diabetic offspring from class I/III heterozygous parents. We confirm that in families from the USA, class I alleles are transmitted preferentially from fathers. However, in family data sets from the UK, Denmark and Sardinia, the reverse is true and maternal transmission is stronger. Furthermore, in the UK family data set, the difference between maternal and paternal transmissions is significant (P<0.05). It is therefore unlikely that 'maternal imprinting' alone explains the parent-of-origin effects in IDDM2-encoded predisposition to type 1 diabetes, at least not in the UK. There is a relationship between VNTR class (allele length) and insulin gene expression, though some results from different studies are conflicting. In the human adult cadaveric pancreas, we confirm our preliminary results that class III alleles are associated with lower levels of insulin mRNA in vivo. Similar results have been obtained independently in human foetal pancreas samples. It is difficult to explain how these marginally lower levels of insulin expression could account for the observed VNTR class III-encoded protective effect, Perhaps the site of action of IDDM2, mediated by VNTR allelic variation, is not the pancreas but some other organ such as the thymus. (C) 1996 Academic Press Limited
引用
收藏
页码:415 / 421
页数:7
相关论文
共 33 条
  • [1] INSULIN GENE REGION-ENCODED SUSCEPTIBILITY TO TYPE-1 DIABETES IS NOT RESTRICTED TO HLA-DR4-POSITIVE INDIVIDUALS
    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
    [J]. NATURE GENETICS, 1992, 2 (03) : 212 - 215
  • [2] THE HIGHLY POLYMORPHIC REGION NEAR THE HUMAN INSULIN GENE IS COMPOSED OF SIMPLE TANDEMLY REPEATING SEQUENCES
    BELL, GI
    SELBY, MJ
    RUTTER, WJ
    [J]. NATURE, 1982, 295 (5844) : 31 - 35
  • [3] A POLYMORPHIC LOCUS NEAR THE HUMAN INSULIN GENE IS ASSOCIATED WITH INSULIN-DEPENDENT DIABETES-MELLITUS
    BELL, GI
    HORITA, S
    KARAM, JH
    [J]. DIABETES, 1984, 33 (02) : 176 - 183
  • [4] SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS
    BENNETT, ST
    LUCASSEN, AM
    GOUGH, SCL
    POWELL, EE
    UNDLIEN, DE
    PRITCHARD, LE
    MERRIMAN, ME
    KAWAGUCHI, Y
    DRONSFIELD, MJ
    POCIOT, F
    NERUP, J
    BOUZEKRI, N
    CAMBONTHOMSEN, A
    RONNINGEN, KS
    BARNETT, AH
    BAIN, SC
    TODD, JA
    [J]. NATURE GENETICS, 1995, 9 (03) : 284 - 292
  • [5] INSULIN EXPRESSION - IS VNTR ALLELE-698 REALLY ANOMALOUS - REPLY
    BENNETT, ST
    LUCASSEN, AM
    GOUGH, SCL
    POWELL, EE
    PRITCHARD, LE
    MERRIMAN, ME
    KAWAGUCHI, Y
    TODD, JA
    UNDLIEN, DE
    RONNINGEN, KS
    POCIOT, F
    NERUP, J
    BOUZEKRI, N
    CAMBONTHOMSEN, A
    DRONSFIELD, MJ
    BARNETT, AH
    BAIN, SC
    [J]. NATURE GENETICS, 1995, 10 (04) : 379 - 380
  • [6] BENNETT ST, 1996, IN PRESS PCR ESSENTI
  • [7] LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33
    COPEMAN, JB
    CUCCA, F
    HEARNE, CM
    CORNALL, RJ
    REED, PW
    RONNINGEN, KS
    UNDLIEN, DE
    NISTICO, L
    BUZZETTI, R
    TOSI, R
    POCIOT, F
    NERUP, J
    CORNELIS, F
    BARNETT, AH
    BAIN, SC
    TODD, JA
    [J]. NATURE GENETICS, 1995, 9 (01) : 80 - 85
  • [8] CUCCA F, 1996, HLA MHC GENES MOL FU
  • [9] A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES
    DAVIES, JL
    KAWAGUCHI, Y
    BENNETT, ST
    COPEMAN, JB
    CORDELL, HJ
    PRITCHARD, LE
    REED, PW
    GOUGH, SCL
    JENKINS, SC
    PALMER, SM
    BALFOUR, KM
    ROWE, BR
    FARRALL, M
    BARNETT, AH
    BAIN, SC
    TODD, JA
    [J]. NATURE, 1994, 371 (6493) : 130 - 136
  • [10] A LOCUS ON CHROMOSOME 15Q26 (IDDM3) PRODUCES SUSCEPTIBILITY TO INSULIN-DEPENDENT DIABETES-MELLITUS
    FIELD, LL
    TOBIAS, R
    MAGNUS, T
    [J]. NATURE GENETICS, 1994, 8 (02) : 189 - 194