Mayya Vinay K, Duchaine Thomas F
Goodman Cancer Research Centre and Department of Biochemistry, McGill University, Montreal, QC, Canada.
Front Genet. 2019 Jan 24;10:6. doi: 10.3389/fgene.2019.00006. eCollection 2019.
The sequences and structures of 3'-untranslated regions (3'UTRs) of messenger RNAs govern their stability, localization, and expression. 3'UTR regulatory elements are recognized by a wide variety of -acting factors that include microRNAs (miRNAs), their associated machinery, and RNA-binding proteins (RBPs). In turn, these factors instigate common mechanistic strategies to execute the regulatory programs encoded by 3'UTRs. Here, we review classes of factors that recognize 3'UTR regulatory elements and the effector machineries they guide toward mRNAs to dictate their expression and fate. We outline illustrative examples of competitive, cooperative, and coordinated interplay such as mRNA localization and localized translation. We further review the recent advances in the study of mRNP granules and phase transition, and their possible significance for the functions of 3'UTRs. Finally, we highlight some of the most recent strategies aimed at deciphering the complexity of the regulatory codes of 3'UTRs, and identify some of the important remaining challenges.
信使核糖核酸(mRNA)3'非翻译区(3'UTR)的序列和结构决定了其稳定性、定位和表达。3'UTR调控元件可被多种反式作用因子识别,这些因子包括微小RNA(miRNA)、其相关机制以及RNA结合蛋白(RBP)。反过来,这些因子会启动常见的机制策略来执行由3'UTR编码的调控程序。在此,我们综述了识别3'UTR调控元件的各类因子以及它们导向mRNA以决定其表达和命运的效应机制。我们概述了竞争性、协同性和协调性相互作用的示例,如mRNA定位和局部翻译。我们还进一步综述了mRNP颗粒和相变研究的最新进展及其对3'UTR功能的潜在意义。最后,我们重点介绍了一些旨在破解3'UTR调控密码复杂性的最新策略,并指出了一些尚存的重要挑战。