Soles Lindsey V, Shi Yongsheng
Department of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, United States.
Front Genet. 2021 Feb 4;12:637705. doi: 10.3389/fgene.2021.637705. eCollection 2021.
The majority of eukaryotic genes produce multiple mRNA isoforms by using alternative poly(A) sites in a process called alternative polyadenylation (APA). APA is a dynamic process that is highly regulated in development and in response to extrinsic or intrinsic stimuli. Mis-regulation of APA has been linked to a wide variety of diseases, including cancer, neurological and immunological disorders. Since the first example of APA was described 40 years ago, the regulatory mechanisms of APA have been actively investigated. Conventionally, research in this area has focused primarily on the roles of regulatory cis-elements and trans-acting RNA-binding proteins. Recent studies, however, have revealed important functions for epigenetic mechanisms, including DNA and histone modifications and higher-order chromatin structures, in APA regulation. Here we will discuss these recent findings and their implications for our understanding of the crosstalk between epigenetics and mRNA 3'-end processing.
大多数真核基因通过在一个称为可变聚腺苷酸化(APA)的过程中使用可变聚(A)位点来产生多种mRNA异构体。APA是一个动态过程,在发育过程以及对外源或内在刺激的反应中受到高度调控。APA的失调与多种疾病有关,包括癌症、神经和免疫紊乱。自从40年前首次描述APA的例子以来,人们一直在积极研究APA的调控机制。传统上,该领域的研究主要集中在调控顺式元件和反式作用RNA结合蛋白的作用上。然而,最近的研究揭示了表观遗传机制在APA调控中的重要功能,包括DNA和组蛋白修饰以及高阶染色质结构。在这里,我们将讨论这些最新发现及其对我们理解表观遗传学与mRNA 3'末端加工之间相互作用的意义。