Transcription factors T-bet and Runx3 cooperate to activate lfng and silence ll4 in T helper type 1 cells

被引:399
作者
Djuretic, Ivana M.
Levanon, Ditsa
Negreanu, Varda
Groner, Yoram
Rao, Anjana
Ansel, K. Mark [1 ]
机构
[1] Harvard Univ, Sch Med, Boston, MA 02115 USA
[2] CBR, Biomed Res Inst, Boston, MA 02115 USA
[3] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
关键词
D O I
10.1038/ni1424
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell differentiation involves activation and silencing of lineage-specific genes. Here we show that the transcription factor Runx3 is induced in T helper type 1 (T(H)1) cells in a T-bet-dependent manner, and that both transcription factors T-bet and Runx3 are required for maximal production of interferon-gamma (IFN-gamma) and silencing of the gene encoding interleukin 4 (Il4) in T(H)1 cells. T-bet does not repress Il4 in Runx3- deficient T(H)2 cells, but coexpression of Runx3 and T-bet induces potent repression in those cells. Both T-bet and Runx3 bind to the Ifng promoter and the Il4 silencer, and deletion of the silencer decreases the sensitivity of Il4 to repression by either factor. Our data indicate that cytokine gene expression in TH1 cells may be controlled by a feed-forward regulatory circuit in which T-bet induces Runx3 and then 'partners' with Runx3 to direct lineage-specific gene activation and silencing.
引用
收藏
页码:145 / 153
页数:9
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