FOXP3型
转录因子
生物
细胞生物学
基因
转录调控
基因表达调控
遗传学
免疫系统
作者
Dipayan Rudra,Paul deRoos,Ashutosh Chaudhry,Rachel Niec,Aaron Arvey,Robert Samstein,Christina S. Leslie,Scott A. Shaffer,David R. Goodlett,Alexander Y. Rudensky
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2012-08-26
卷期号:13 (10): 1010-1019
被引量:430
摘要
The transcription factor Foxp3 is indispensible for the differentiation and function of regulatory T cells (T(reg) cells). To gain insights into the molecular mechanisms of Foxp3-mediated gene expression, we purified Foxp3 complexes and explored their composition. Biochemical and mass-spectrometric analyses revealed that Foxp3 forms multiprotein complexes of 400-800 kDa or larger and identified 361 associated proteins, ∼30% of which were transcription related. Foxp3 directly regulated expression of a large proportion of the genes encoding its cofactors. Some transcription factor partners of Foxp3 facilitated its expression. Functional analysis of the cooperation of Foxp3 with one such partner, GATA-3, provided additional evidence for a network of transcriptional regulation afforded by Foxp3 and its associates to control distinct aspects of T(reg) cell biology.
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