Laboratory of Host Defense, WPI Immunology Frontier Research Center (IFReC), Osaka University, Osaka 565-0874, Japan.
Department of Host Defense, Division of Host Defense, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka 565-0874, Japan; email:
Annu Rev Immunol. 2021 Apr 26;39:481-509. doi: 10.1146/annurev-immunol-101819-075147. Epub 2021 Feb 12.
Posttranscriptional control of mRNA regulates various biological processes, including inflammatory and immune responses. RNA-binding proteins (RBPs) bind regulatory elements in the 3' untranslated regions (UTRs) of mRNA and regulate mRNA turnover and translation. In particular, eight RBPs (TTP, AUF1, KSRP, TIA-1/TIAR, Roquin, Regnase, HuR, and Arid5a) have been extensively studied and are key posttranscriptional regulators of inflammation and immune responses. These RBPs sometimes collaboratively or competitively bind the same target mRNA to enhance or dampen regulatory activities. These RBPs can also bind their own 3' UTRs to negatively or positively regulate their expression. Both upstream signaling pathways and microRNA regulation shape the interactions between RBPs and target RNA. Dysregulation of RBPs results in chronic inflammation and autoimmunity. Here, we summarize the functional roles of these eight RBPs in immunity and their associated diseases.
mRNA 的转录后调控控制着各种生物过程,包括炎症和免疫反应。RNA 结合蛋白 (RBP) 结合 mRNA 3' 非翻译区 (UTR) 中的调节元件,调节 mRNA 的周转和翻译。特别是,有八种 RBP(TTP、AUF1、KSRP、TIA-1/TIAR、Roquin、Regnase、HuR 和 Arid5a)已经得到了广泛的研究,是炎症和免疫反应的关键转录后调节因子。这些 RBP 有时会协同或竞争地结合相同的靶 mRNA,以增强或抑制调节活性。这些 RBP 还可以结合自身的 3'UTR,从而负向或正向调节自身的表达。上游信号通路和 microRNA 调节都影响 RBP 和靶 RNA 之间的相互作用。RBP 的失调会导致慢性炎症和自身免疫。在这里,我们总结了这八种 RBP 在免疫中的功能作用及其相关疾病。