Schwerk Johannes, Savan Ram
Department of Immunology, University of Washington, Seattle, WA 98109.
Department of Immunology, University of Washington, Seattle, WA 98109
J Immunol. 2015 Oct 1;195(7):2963-71. doi: 10.4049/jimmunol.1500756.
Gene expression programs undergo constant regulation to quickly adjust to environmental stimuli that alter the physiological status of the cell, like cellular stress or infection. Gene expression is tightly regulated by multilayered regulatory elements acting in both cis and trans. Posttranscriptional regulation of the 3' untranslated region (UTR) is a powerful regulatory process that determines the rate of protein translation from mRNA. Regulatory elements targeting the 3' UTR include microRNAs, RNA-binding proteins, and long noncoding RNAs, which dramatically alter the immune response. We provide an overview of our current understanding of posttranscriptional regulation of immune gene expression. The focus of this review is on regulatory elements that target the 3' UTR. We delineate how the synergistic or antagonistic interactions of posttranscriptional regulators determine gene expression levels and how dysregulation of 3' UTR-mediated posttranscriptional control associates with human diseases.
基因表达程序不断受到调控,以快速适应改变细胞生理状态的环境刺激,如细胞应激或感染。基因表达受到顺式和反式作用的多层调控元件的严格调控。3'非翻译区(UTR)的转录后调控是一个强大的调控过程,它决定了从mRNA翻译蛋白质的速率。靶向3'UTR的调控元件包括微小RNA、RNA结合蛋白和长链非编码RNA,它们会显著改变免疫反应。我们概述了目前对免疫基因表达转录后调控的理解。本综述的重点是靶向3'UTR的调控元件。我们阐述了转录后调节因子的协同或拮抗相互作用如何决定基因表达水平,以及3'UTR介导的转录后控制失调如何与人类疾病相关联。