Cooperative activation of transcription by autoimmune regulator AIRE and CBP

被引:53
|
作者
Pitkänen, J
Rebane, A
Rowell, J
Murumägi, A
Ströbel, P
Möll, K
Saare, M
Heikkilä, J
Doucas, V
Marx, A
Peterson, P [1 ]
机构
[1] Tampere Univ, Inst Med Technol, FIN-33101 Tampere, Finland
[2] Tampere Univ Hosp, Tampere, Finland
[3] Univ Tartu, IGMP, EE-50090 Tartu, Estonia
[4] Univ Wurzburg, Inst Pathol, D-8700 Wurzburg, Germany
[5] Coll France, Inst Biol, F-75231 Paris, France
基金
英国惠康基金;
关键词
APECED; PML; nuclear bodies;
D O I
10.1016/j.bbrc.2005.05.187
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
Autoimmune regulator (AIRE) is a transcriptional regulator that is believed to control the expression of tissue-specific genes in the thymus. Mutated AIRE is responsible for onset of the hereditary autoimmune disease APECED. AIRE is able to form nuclear bodies (NBs) and interacts with the ubiquitous transcriptional coactivator CBP. In this paper, we show that CBP and AIRE synergistically activate transcription on different promoter reporters whereas AIRE gene mutation R257X, found in APECED patients, interferes with this coactivation effect. Furthermore, the overexpression of AIRE and CBP collaboratively enhance endogenous IFN beta mRNA expression. The immunohistochemical studies suggest that CBP, depending on the balance of nuclear proteins, is a component of AIRE NBs. We also show that AIRE NBs are devoid of active chromatin and, therefore, not sites of transcription. In addition, we demonstrate by 3D analyses that AIRE and CBP, when colocalizing, are located spatially differently within AIRE NBs. In conclusion, our data suggest that AIRE activates transcription of the target genes, i.e., autoantigens in collaboration with CBP and that this activation occurs outside of AIRE NBs. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:944 / 953
页数:10
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