Aire's Partners in the Molecular Control of Immunological Tolerance

被引:242
作者
Abramson, Jakub [1 ]
Giraud, Matthieu [1 ]
Benoist, Christophe [1 ,2 ]
Mathis, Diane [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] Broad Inst, Boston, MA 02115 USA
[3] Harvard Stem Cell Inst, Boston, MA 02115 USA
关键词
THYMIC EPITHELIAL-CELLS; TRANSCRIPTIONAL ELONGATION; GENE-EXPRESSION; II TRANSCRIPTION; T-CELLS; BINDING; PROTEIN; PHOSPHORYLATION; AUTOIMMUNITY; BREAKS;
D O I
10.1016/j.cell.2009.12.030
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
Aire induces the expression of a battery of peripheral-tissue self-antigens (PTAs) in thymic stromal cells, promoting the clonal deletion of differentiating T cells that recognize them. Just how Aire targets and induces PTA transcripts remains largely undefined. Screening via Aire-targeted coimmunoprecipitation followed by mass spectrometry, and validating by multiple RNAi-mediated knockdown approaches, we identified a large set of proteins that associate with Aire. They fall into four major functional classes: nuclear transport, chromatin binding/structure, transcription and pre-mRNA processing. One set of Aire interactions centered on DNA protein kinase and a group of proteins it partners with to resolve DNA double-stranded breaks or promote transcriptional elongation. Another set of interactions was focused on the pre-mRNA splicing and maturation machinery, potentially explaining the markedly more effective processing of PTA transcripts in the presence of Aire. These findings suggest a model to explain Aire's widespread targeting and induction of weakly transcribed chromatin regions.
引用
收藏
页码:123 / 135
页数:13
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