Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes

被引:26
作者
Bassuny, WM
Ihara, K [1 ]
Matsuura, N
Ahmed, S
Kohno, H
Kuromaru, R
Miyako, K
Hara, T
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Fukuoka 812, Japan
[2] Kitasato Univ, Sch Med, Dept Pediat, Sagamihara, Kanagawa 228, Japan
[3] Fukuoka Childrens Hosp, Dept Endocrinol & Metab, Fukuoka, Japan
[4] Kyushu Univ, Dept Pediat, Higashi Ku, Fukuoka 8128582, Japan
关键词
NRAMP1; CTLA-4; polymorphism; type; 1; diabetes;
D O I
10.1007/s00251-002-0459-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Natural resistance-associated macrophage protein 1 (NRAMP1) has an important role in regulating macrophage functions that affect innate resistance as well as immune responses. We analyzed the microsatellite polymorphism in the promoter region of the human NRAMP1 gene in 206 type 1 diabetes patients and 200 normal children to determine whether this polymorphism might be associated with type 1 diabetes in the Japanese population. The frequency of allele 2 (180 bp) of the promoter microsatellite polymorphism of the NRAMP1 gene was slightly lower in the early-onset population (2-10 years of age) of type 1 diabetes patients than in controls, although the difference did not reach statistical significance. The association study of the cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) gene, located near the NRAMP1 gene, and type 1 diabetes showed that the CTLA-4 gene significantly contributed to the development of type 1 diabetes, whereas NRAMP1 had an additional effect on the onset of type 1 diabetes in the young population.
引用
收藏
页码:282 / 285
页数:4
相关论文
共 26 条
[1]   Association of CTLA-4 but not CD28 gene polymorphisms with systemic lupus erythematosus in the Japanese population [J].
Ahmed, S ;
Ihara, K ;
Kanemitsu, S ;
Nakashima, H ;
Otsuka, T ;
Tsuzaka, K ;
Takeuchi, T ;
Hara, T .
RHEUMATOLOGY, 2001, 40 (06) :662-667
[2]   Genetic regulation of macrophage activation:: understanding the function of Nramp1 (= Ity/Lsh/Bcg) [J].
Blackwell, JM ;
Searle, S .
IMMUNOLOGY LETTERS, 1999, 65 (1-2) :73-80
[3]   HUMAN NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN - CDNA CLONING, CHROMOSOMAL MAPPING, GENOMIC ORGANIZATION, AND TISSUE-SPECIFIC EXPRESSION [J].
CELLIER, M ;
GOVONI, G ;
VIDAL, S ;
KWAN, T ;
GROULX, N ;
LIU, J ;
SANCHEZ, F ;
SKAMENE, E ;
SCHURR, E ;
GROS, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (05) :1741-1752
[4]   Genetic analysis of chromosome 2 in type 1 diabetes -: Analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster [J].
Esposito, L ;
Hill, NJ ;
Pritchard, LE ;
Cucca, F ;
Muxworthy, C ;
Merriman, ME ;
Wilson, A ;
Julier, C ;
Delepine, M ;
Tuomilehto, J ;
Tuomilehto-Wolf, E ;
Ionesco-Tirgoviste, C ;
Nistico', L ;
Buzzetti, R ;
Pozzilli, P ;
Ferrari, M ;
Bosi, E ;
Pociot, F ;
Nerup, J ;
Bain, SC ;
Todd, JA .
DIABETES, 1998, 47 (11) :1797-1799
[5]   Genetic linkage and association studies of Type I diabetes: challenges and rewards [J].
Field, LL .
DIABETOLOGIA, 2002, 45 (01) :21-35
[6]  
Gavin JR, 1997, DIABETES CARE, V20, P1183
[7]   Identification of novel alleles at a polymorphic microsatellite repeat region in the human NRAMP1 gene promoter:: analysis of allele frequencies in primary biliary cirrhosis [J].
Graham, AM ;
Dollinger, MM ;
Howie, SEM ;
Harrison, DJ .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (02) :150-152
[8]   Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family [J].
Greenwood, CMT ;
Fujiwara, TM ;
Boothroyd, LJ ;
Miller, MA ;
Frappier, D ;
Fanning, EA ;
Schurr, E ;
Morgan, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) :405-416
[9]   NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans [J].
Hill, NJ ;
Lyons, PA ;
Armitage, N ;
Todd, JA ;
Wicker, LS ;
Peterson, LB .
DIABETES, 2000, 49 (10) :1744-1747
[10]   The HLA-E locus is associated with age at onset and susceptibility to type 1 diabetes mellitus [J].
Hodgkinson, AD ;
Millward, BA ;
Demaine, AG .
HUMAN IMMUNOLOGY, 2000, 61 (03) :290-295