Cooperation of RNA-Binding Proteins - a Focus on Roquin Function in T Cells

被引:6
作者
Behrens, Gesine [1 ]
Heissmeyer, Vigo [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Fac Med, Biomed Ctr BMC, Inst Immunol, Planegg Martinsried, Germany
[2] Helmholtz Zentrum Munchen, Res Unit Mol Immune Regulat, Munich, Germany
关键词
RNA-binding proteins; Roquin; Regnase-1; post-transcriptional gene regulation; cooperativity; autoimmunity; tumor immunity; CONSTITUTIVE-DECAY ELEMENT; MESSENGER-RNA; TRANSCRIPTION FACTOR; REGNASE-1; DIFFERENTIATION; NFAT; AUTOIMMUNITY; RECOGNITION; SUPPRESSES; ACTIVATION;
D O I
10.3389/fimmu.2022.839762
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Post-transcriptional gene regulation by RNA-binding proteins (RBPs) is important in the prevention of inflammatory and autoimmune diseases. With respect to T cell activation and differentiation, the RBPs Roquin-1/2 and Regnase-1 play pivotal roles by inducing degradation and/or translational silencing of target mRNAs. These targets encode important proinflammatory mediators and thus Roquin and Regnase-1 functions dampen cellular programs that can lead to inflammation and autoimmune disease. Recent findings demonstrate direct physical interaction of both RBPs. Here, we propose that cooperativity of trans-acting factors may be more generally used to reinforce the regulatory impact on selected targets and promote specific cell fate decisions. We develop this concept for Roquin and Regnase-1 function in resting and activated T cells and discuss the involvement in autoimmunity as well as how the therapeutic potential can be used in anti-tumor therapies.
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页数:8
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