Post-transcriptional regulatory networks in immunity

被引:92
作者
Ivanov, Pavel [1 ,2 ]
Anderson, Paul [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
post-transcriptional regulation; RNA-binding proteins; mRNA decay; microRNAs; translational control; inflammation; RNA-BINDING-PROTEIN; TUMOR-NECROSIS-FACTOR; AU-RICH-ELEMENT; FACTOR MESSENGER-RNA; NF-KAPPA-B; PLASMACYTOID DENDRITIC CELLS; 3' UNTRANSLATED REGION; 60S RIBOSOMAL-SUBUNIT; IL-2; GENE-EXPRESSION; INTERFERON-BETA GENE;
D O I
10.1111/imr.12051
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Post-transcriptional mechanisms that modulate global and/or transcript-specific mRNA stability and translation contribute to the rapid and flexible control of gene expression in immune effector cells. These mechanisms rely on RNA-binding proteins (RBPs) that direct regulatory complexes (e.g. exosomes, deadenylases, decapping complexes, RNA-induced silencing complexes) to the 3-untranslated regions of specific immune transcripts. Here, we review the surprising variety of post-transcriptional control mechanisms that contribute to gene expression in the immune system and discuss how defects in these pathways can contribute to autoimmune disease.
引用
收藏
页码:253 / 272
页数:20
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