Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33

被引:92
作者
Marron, MP
Zeidler, A
Raffel, LJ
Eckenrode, SE
Yang, JJ
Hopkins, DI
Garchon, HJ
Jacob, CO
Serrano-Rios, M
Larrad, MTM
Park, Y
Bach, JF
Rotter, JI
Yang, MCK
She, JX
机构
[1] Univ Florida, Coll Med, Dept Pathol Immunol & Lab Med, Gainesville, FL 32610 USA
[2] Univ Florida, Ctr Mammalian Genet, Gainesville, FL 32610 USA
[3] Univ Florida, Diabet Ctr Excellence, Gainesville, FL 32610 USA
[4] Univ Florida, Dept Stat, Gainesville, FL 32610 USA
[5] Univ So Calif, Sch Med, Dept Med, Los Angeles, CA 90033 USA
[6] Cedars Sinai Med Ctr, Dept Pediat, Los Angeles, CA 90048 USA
[7] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
[8] Univ Calif Los Angeles, Los Angeles, CA USA
[9] Ctr Assoc Claude Bernard, INSERM, U25, Unite Rech, Paris, France
[10] Univ Complutense Madrid, Fac Med, E-28040 Madrid, Spain
[11] Hanyang Univ, Seoul 133791, South Korea
关键词
D O I
10.2337/diabetes.49.3.492
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Polymorphic markers within the CTLA4 gene on chromosome 2q33 have been shown to be associated with type 1 diabetes. Therefore, a gene responsible for the disease (IDDM12) most likely lies within a region of <1-2 cM of CTLA4. To define more precisely the IDDM12 interval, we genotyped a multiethnic (U.S. Caucasian, Mexican-American, French, Spanish, Korean, and Chinese) collection of 178 simplex and 350 multiplex families for 10 polymorphic markers within a genomic interval of similar to 300 kb, which contains the candidate genes CTLA4 and CD28. The order of these markers (D2S346, CD28, GGAA19E07, D2S307, D2S72, CTLA4, D2S105, and GATA52A04) was determined by sequence tagged site content mapping of bacterial artificial chromosome (BAC) and yeast artificial chromosome (YAC) clones. The transmission disequilibrium test (TDT) analyses of our data revealed significant association/linkage with three markers within CTLA4 and two immediate flanking markers (D2S72 and D2S105) on each side of CTLA4 but not with more distant markers including the candidate gene CD28. Tsp analyses revealed significant association only with the three polymorphic markers within the CTLA4 gene. The markers linked and associated with type 1 diabetes are contained within a phagemid artificial chromosome clone of 100 kb, suggesting that the IDDM12 locus is either CTLA4 or an unknown gene in very close proximity.
引用
收藏
页码:492 / 499
页数:8
相关论文
共 70 条
[1]   CD28-B7 INTERACTIONS IN T-CELL ACTIVATION [J].
ALLISON, JP .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (03) :414-419
[2]  
[Anonymous], 1990, GENETIC DATA ANAL
[3]  
ATKINSON MA, 1994, NEW ENGL J MED, V331, P1428
[4]   Association of CTLA-4 gene A-G polymorphism (IDDM12 locus) with acute-onset and insulin-depleted IDDM as well as autoimmune thyroid disease (Graves disease and Hashimoto's thyroiditis) in the Japanese population [J].
Awata, T ;
Kurihara, S ;
Iitaka, M ;
Takei, S ;
Inoue, I ;
Ishii, C ;
Negishi, K ;
Izumida, T ;
Yoshida, Y ;
Hagura, R ;
Kuzuya, N ;
Kanazawa, Y ;
Katayama, S .
DIABETES, 1998, 47 (01) :128-129
[5]   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
[6]   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
[7]   SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS [J].
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 .
NATURE GENETICS, 1995, 9 (03) :284-292
[8]   Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele [J].
Bennett, ST ;
Wilson, AJ ;
Esposito, L ;
Bouzekri, N ;
Undlien, DE ;
Cucca, F ;
Nistico, L ;
Buzzetti, R ;
Bosi, E ;
Pociot, F ;
Nerup, J ;
CambonThomsen, A ;
Pugliese, A ;
Shield, JPH ;
McKinney, PA ;
Bain, SC ;
Polychronakos, C ;
Todd, JA ;
Pozzilli, P ;
Visalli, N ;
Baroni, M ;
Fioriti, E ;
Mesturino, C ;
Signore, A ;
Cavallo, M ;
Lucentini, L ;
Matteoli, M ;
Crino, A ;
Teodonio, C ;
Amoretti, R ;
Tombesi, A ;
Ruggeri, M ;
Pisano, L ;
Suraci, C ;
Pennafina, M ;
Boscherini, B ;
Stoduto, S ;
Fonte, M ;
Mancabitti, M ;
Multari, G ;
Suppa, M ;
DeMattia, G ;
Faldetta, MC ;
Laurenti, O ;
Marietti, G ;
Pitocco, D ;
Ferrazzoli, F ;
Bizzarri, C ;
Ghirlanda, G .
NATURE GENETICS, 1997, 17 (03) :350-352
[9]   Paternally transmitted IDDM2 influences diabetes susceptibility despite biallelic expression of the insulin gene in human pancreas [J].
Bui, MM ;
Luo, DF ;
She, JY ;
Maclaren, NK ;
Muir, A ;
Thomson, G ;
She, JX .
JOURNAL OF AUTOIMMUNITY, 1996, 9 (01) :97-103
[10]   MOLECULAR LINKAGE OF THE HUMAN CTLA4 AND CD28 IG-SUPERFAMILY GENES IN YEAST ARTIFICIAL CHROMOSOMES [J].
BUONAVISTA, N ;
BALZANO, C ;
PONTAROTTI, P ;
LEPASLIER, D ;
GOLSTEIN, P .
GENOMICS, 1992, 13 (03) :856-861