A second susceptibility gene for developing rheumatoid arthritis in the human MHC is localized within a 70-kb interval telomeric of the TNF genes in the HLA class III region

被引:90
作者
Ota, M
Katsuyama, Y
Kimura, A
Tsuchiya, K
Kondo, M
Naruse, T
Mizuki, N
Itoh, K
Sasazuki, T
Inoko, H [1 ]
机构
[1] Tokai Univ, Sch Med, Dept Genet Informat, Div Mol Life Sci, Isehara, Kanagawa 2591193, Japan
[2] Yokohama City Univ, Sch Med, Dept Ophthalmol, Yokohama, Kanagawa 232, Japan
[3] Kurume Univ, Sch Med, Dept Immunol, Kurume, Fukuoka 830, Japan
[4] Fukuoka Chuo Hosp, Div Orthopaed Surg, Fukuoka, Japan
[5] Kyushu Univ, Sch Med, Dept Orthoped Surg, Fukuoka 812, Japan
[6] Kyushu Univ, Sch Med, Med Inst Bioregulat, Dept Genet, Fukuoka 812, Japan
[7] Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Pathogenesis, Div Adult Dis, Tokyo, Japan
[8] Shinshu Univ Hosp, Dept Pharm, Matsumoto, Nagano, Japan
[9] Shinshu Univ, Sch Med, Dept Legal Med, Matsumoto, Nagano 390, Japan
[10] Shinshu Univ, Sch Med, Inst Organ Transplants Reconstruct Med & Tissue E, Matsumoto, Nagano 390, Japan
关键词
D O I
10.1006/geno.2000.6371
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Rheumatoid arthritis (RA) is a chronic inflammatory joint disease with a multifactorial genetic basis. However, pathogenic genes for RA other than the human leukocyte antigen (HLA)-DRB1 gene have yet to be identified. Here, we investigated whether there is a second susceptibility locus for RA within the human major histocompatibility complex using 18 microsatellite markers distributed from the centromeric (HSET) to the telomeric end (P5-15) of the 3.6-Mb HLA region. Statistical studies of associated alleles on each microsatellite locus showed that one pathogenic gene far RA in the HLA region is localized in the DRB1 gene, as expected. Further, a second susceptibility gene of RA was suggested to be present in the HLA class III region, narrowed to 70 kb, that is just telomeric of the TNF gene cluster (TNFA and LTA) and that is located between the microsatellites TNFa and C1-2-A. In this critical segment, four expressed genes have been thus far identified, NFKBIL1 (I kappa BL), ATP6G, BAT1, and MICB, all of which are candidate genes for determining susceptibility to RA. These results exclude the possibility of involvement of the TNFA genes (TNF-alpha) in the development of RA, which was suggested previously to be a strong candidate for RA in the class III region. (C) 2001 Academic Press.
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页码:263 / 270
页数:8
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