Department of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, building 1130, 8000 Aarhus C, Denmark.
Department of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, building 1130, 8000 Aarhus C, Denmark
Philos Trans R Soc Lond B Biol Sci. 2018 Nov 5;373(1762):20180169. doi: 10.1098/rstb.2018.0169.
A polyA (pA) tail is an essential modification added to the 3' ends of a wide range of RNAs at different stages of their metabolism. Here, we describe the main sources of polyadenylation and outline their underlying biochemical interactions within the nuclei of budding yeast , human cells and, when relevant, the fission yeast Polyadenylation mediated by the Trf4/5 enzymes, and their human homologues PAPD5/7, typically leads to the 3'-end trimming or complete decay of non-coding RNAs. By contrast, the primary function of canonical pA polymerases (PAPs) is to produce stable and nuclear export-competent mRNAs. However, this dichotomy is becoming increasingly blurred, at least in and human cells, where polyadenylation mediated by canonical PAPs may also result in transcript decay.This article is part of the theme issue '5' and 3' modifications controlling RNA degradation'.
多聚腺苷酸化 (pA) 尾是在各种 RNA 代谢的不同阶段添加到其 3' 末端的一种必需修饰。在这里,我们描述了多聚腺苷酸化的主要来源,并概述了它们在芽殖酵母、人类细胞核内的基本生化相互作用,以及在相关情况下,裂殖酵母中的生化相互作用。由 Trf4/5 酶及其人类同源物 PAPD5/7 介导的多聚腺苷酸化通常导致非编码 RNA 的 3' 末端修剪或完全降解。相比之下,典型的核内 poly(A) 聚合酶 (PAPs) 的主要功能是产生稳定的和具有核输出能力的 mRNAs。然而,这种二分法在至少在 和人类细胞中变得越来越模糊,其中由典型的 PAP 介导的多聚腺苷酸化也可能导致转录物的降解。本文是主题问题“5' 和 3' 修饰控制 RNA 降解”的一部分。