BRG1 is indispensable for IFN-γ-induced TRIM22 expression, which is dependent on the recruitment of IRF-1

被引:6
|
作者
Wang, Yaxin [1 ,2 ]
Gao, Bo [1 ,2 ]
Xu, Wei [1 ,2 ]
Xiong, Sidong [1 ,2 ,3 ]
机构
[1] Soochow Univ, Inst Biol, Jiangsu Key Lab Infect & Immun Inst, Suzhou 215006, Peoples R China
[2] Soochow Univ, Inst Med Sci, Jiangsu Key Lab Infect & Immun Inst, Suzhou 215006, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Immunol, Inst Immunobiol, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
TRIM22; IFN-gamma; BRG1; IRF-1; Recruitment; REGULATORY FACTOR-I; E3 UBIQUITIN LIGASE; B-VIRUS INFECTION; INTERFERON-GAMMA; HIV-1; INFECTION; FAMILY PROTEINS; CHROMATIN; PROMOTER; ACTIVATION; MECHANISMS;
D O I
10.1016/j.bbrc.2011.06.022
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 modification of chromatin structure is increasingly recognized to be an important facet of transcriptional regulation. Here, we report that Brahma-related gene 1 (BRG1), a chromatin remodeling enzyme, plays a crucial role in IFN-gamma-induced TRIM22 expression. Our results showed that IFN-gamma failed to induce TRIM22 expression in BRG1-deficient SW-13 cells, and reconstitution of BRG1 in this cell line could restore IFN-gamma induction of TRIM22. Furthermore, it was revealed that BRG1 absence, per se, did not impair IFN-gamma-induced IRF-1 expression, but blocked its access to TRIM22 promoter, and BRG1-dependent induction of TRIM22 perfectly correlated with BRG1-dependent recruitment of IRF-1 to TRIM22 promoter. We also found that the DNA-dependent ATPase domain of BRG1 was required for TRIM22 expression and IRF-1 recruitment in response to IFN-gamma stimulation, suggesting that BRG1-mediated chromatin remodeling is critical for the IFN-gamma-inducibility of TRIM22 gene. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:549 / 554
页数:6
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