AIRE functions as an E3 ubiquitin ligase

被引:107
作者
Uchida, D
Hatakeyama, S
Matsushima, A
Han, HW
Ishido, S
Hotta, H
Kudoh, J
Shimizu, N
Doucas, V
Nakayama, KI
Kuroda, N
Matsumoto, M
机构
[1] Univ Tokushima, Inst Enzyme Res, Div Mol Immunol, Tokushima 7708503, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Dept Mol & Cellular Biol, Fukuoka 8128582, Japan
[3] Kobe Univ, Grad Sch Med, Dept Genome Sci, Div Microbiol, Kobe, Hyogo 6500017, Japan
[4] Keio Univ, Sch Med, Dept Mol Biol, Tokyo 1608582, Japan
[5] Inst Jacques Monod, Dept Biol Genomes, F-75251 Paris, France
关键词
APECED; self-tolerance; transcriptional regulator; ubiquitylation; PHD domain;
D O I
10.1084/jem.20031291
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune regulator (AIRE) gene mutation is responsible for the development of autoimmune-polyendocrinopathy-candidiasis ectodermal dystrophy, an organ-specific autoimmune disease with monogenic autosomal recessive inheritance. AIRE is predominantly expressed in medullary epithelial cells of the thymus and is considered to play important roles in the establishment of self-tolerance. AIRE contains two plant homeodomain (PHD) domains, and the novel role of PHD as in E3 ubiquitin (Ub) ligase has just emerged. Here we show that the first PHD (PHD1) of AIRE mediates E3 ligase activity. The significance of this finding was underscored by the fact that disease-causing missense mutations in the PHD 1 (C311Y and P326Q) abolished its E3 ligase activity. These results add a novel enzymatic function for AIRE and suggest an indispensable role of the Ub proteasome pathway in the establishment of self-tolerance, in which AIRE is involved.
引用
收藏
页码:167 / 172
页数:6
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