Positional cloning of the APECED gene

被引:992
作者
Nagamine, K
Peterson, P
Scott, HS
Kudoh, J
Minoshima, S
Heino, M
Krohn, KJE
Lalioti, MD
Mullis, PE
Antonarakis, SE
Kawasaki, K
Asakawa, S
Ito, F
Shimizu, N
机构
[1] KEIO UNIV,SCH MED,DEPT MOL BIOL,SHINJUKU KU,TOKYO 160,JAPAN
[2] SETSUNAN UNIV,FAC PHARMACEUT SCI,DEPT BIOCHEM,HIRAKATA,OSAKA 57301,JAPAN
[3] TAMPERE UNIV HOSP,TAMPERE 33101,FINLAND
[4] INST MED TECHNOL,TAMPERE 33101,FINLAND
[5] UNIV GENEVA,SCH MED,DEPT GENET & MICROBIOL,LAB HUMAN MOL GENET,CH-1211 GENEVA 4,SWITZERLAND
[6] CANTONAL HOSP GENEVA,DIV MED GENET,CH-1211 GENEVA 4,SWITZERLAND
[7] UNIV BERN,DEPT PAEDIAT,BERN,SWITZERLAND
关键词
D O I
10.1038/ng1297-393
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autoimmune polyglandular syndrome type I (APS 1, also called APECED) is an autosomal-recessive disorder that maps to human chromosome 21q22.3 between markers D21S49 and D21S171 by linkage studies. We have isolated a novel gene from this region, AIRE (autoimmune regulator), which encodes a protein containing motifs suggestive of a transcription factor including two zinc-finger (PHD-finger) motifs, a proline-rich region and three LXXLL motifs. Two mutations, a C-->T substitution that changes the Arg 257 (CGA) to a stop codon (TGA) and an A-->G substitution that changes the Lys 83 (AAG) to a Glu codon (GAG), were found in this novel gene in Swiss and Finnish APECED patients. The Arg257stop (R257X) is the predominant mutation in Finnish APECED patients, accounting for 10/12 alleles studied. These results indicate that this gene is responsible for the pathogenesis of APECED. The identification of the gene defective in APECED should facilitate the genetic diagnosis and potential treatment of the disease and further enhance our general understanding of the mechanisms underlying autoimmune diseases.
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收藏
页码:393 / 398
页数:6
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