AIRE encodes a nuclear protein co-localizing with cytoskeletal filaments:: altered sub-cellular distribution of mutants lacking the PHD zinc fingers

被引:80
作者
Rinderle, C [1 ]
Christensen, HM [1 ]
Schweiger, S [1 ]
Lehrach, H [1 ]
Yaspo, ML [1 ]
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
关键词
D O I
10.1093/hmg/8.2.277
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene responsible for autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) recently has been positionally cloned to 21q22.3, This novel gene, AIRE, encodes for a predicted 57.7 kDa protein featuring two PHD-type zinc fingers shared by other proteins involved in chromatin-mediated transcriptional regulation. APECED is an autosomal recessive condition characterized by multiple polyendocrinopathies, and the typical triad of APECED symptoms includes hypoparathyroidism, primary adrenocortical failure and chronic mucocutaneous candidiasis, The aetiology of APECED is linked directly to mutations within the coding region of AIRE. These mutations are predicted to lead to truncated forms of the protein lacking at least one of the PHD zinc fingers. In this study, we have investigated the sub-cellular localization of AIRE expressed transiently in COS cells and fibroblasts. We found that AIRE has a dual nuclear and cytoplasmic localization. The wild-type protein is directed to speckled domains in the nucleus and also shows co-localization with cytoskeletal filaments, N-terminal AIRE fragments deleted for the PHD domain show altered nuclear localization, suggesting that the APECED mutations may elicit their primary effects in the nucleus.
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页码:277 / 290
页数:14
相关论文
共 42 条
[1]   An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains [J].
Aaltonen, J ;
Bjorses, P ;
Perheentupa, J ;
HorelliKuitunen, N ;
Palotie, A ;
Peltonen, L ;
Lee, YS ;
Francis, F ;
Hennig, S ;
Thiel, C ;
Lehrach, H ;
Yaspo, ML .
NATURE GENETICS, 1997, 17 (04) :399-403
[2]   AN AUTOSOMAL LOCUS CAUSING AUTOIMMUNE-DISEASE - AUTOIMMUNE POLYGLANDULAR DISEASE TYPE-I ASSIGNED TO CHROMOSOME-21 [J].
AALTONEN, J ;
BJORSES, P ;
SANDKUIJL, L ;
PERHEENTUPA, J ;
PELTONEN, L .
NATURE GENETICS, 1994, 8 (01) :83-87
[3]   THE PHD FINGER - IMPLICATIONS FOR CHROMATIN-MEDIATED TRANSCRIPTIONAL REGULATION [J].
AASLAND, R ;
GIBSON, TJ ;
STEWART, AF .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (02) :56-59
[4]  
AHONEN P, 1985, CLIN GENET, V27, P535, DOI 10.1111/j.1399-0004.1985.tb02037.x
[5]   CLINICAL VARIATION OF AUTOIMMUNE POLYENDOCRINOPATHY CANDIDIASIS ECTODERMAL DYSTROPHY (APECED) IN A SERIES OF 68 PATIENTS [J].
AHONEN, P ;
MYLLARNIEMI, S ;
SIPILA, I ;
PERHEENTUPA, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (26) :1829-1836
[6]   Proteolysis that is inhibited by Hedgehog targets Cubitus interruptus protein to the nucleus and converts it to a repressor [J].
AzaBlanc, P ;
RamirezWeber, FA ;
Laget, MP ;
Schwartz, C ;
Kornberg, TB .
CELL, 1997, 89 (07) :1043-1053
[7]   Going mobile: Microtubule motors and chromosome segregation [J].
Barton, NR ;
Goldstein, LSB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (05) :1735-1742
[8]  
Biesecker L, 1998, NAT GENET, V18, P88, DOI 10.1038/ng0198-88a
[9]   Strike three for GLI3 [J].
Biesecker, LG .
NATURE GENETICS, 1997, 17 (03) :259-260
[10]   Localization of the APECED protein in distinct nuclear structures [J].
Björses, P ;
Pelto-Huikko, M ;
Kaukonen, J ;
Aaltonen, J ;
Peltonen, L ;
Ulmanen, I .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :259-266