Nagamine K, Peterson P, Scott H S, Kudoh J, Minoshima S, Heino M, Krohn K J, Lalioti M D, Mullis P E, Antonarakis S E, Kawasaki K, Asakawa S, Ito F, Shimizu N
Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan.
Nat Genet. 1997 Dec;17(4):393-8. doi: 10.1038/ng1297-393.
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.
自身免疫性多内分泌腺病I型(APS 1,也称为自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良综合征)是一种常染色体隐性疾病,通过连锁研究定位于人类21号染色体21q22.3区域,位于标记D21S49和D21S171之间。我们从该区域分离出一个新基因,AIRE(自身免疫调节因子),它编码一种蛋白质,该蛋白质含有提示转录因子的基序,包括两个锌指(PHD指)基序、一个富含脯氨酸的区域和三个LXXLL基序。在瑞士和芬兰的自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良综合征患者的这个新基因中发现了两个突变,一个是C→T替换,将Arg 257(CGA)变为终止密码子(TGA),另一个是A→G替换,将Lys 83(AAG)变为Glu密码子(GAG)。Arg257stop(R257X)是芬兰自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良综合征患者中的主要突变,在所研究的12个等位基因中占10个。这些结果表明该基因是自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良综合征发病机制的原因。鉴定自身免疫性多内分泌腺病-念珠菌病-外胚层营养不良综合征中缺陷的基因应有助于该疾病的基因诊断和潜在治疗,并进一步加深我们对自身免疫性疾病潜在机制的总体理解。