Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, RI, United States of America.
Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, RI, United States of America; Center for Computational Molecular Biology, Brown University, Providence, RI, United States of America.
Biochim Biophys Acta Gene Regul Mech. 2019 Nov-Dec;1862(11-12):194439. doi: 10.1016/j.bbagrm.2019.194439. Epub 2019 Nov 1.
RNA splicing, the process through which intervening segments of noncoding RNA (introns) are excised from pre-mRNAs to allow for the formation of a mature mRNA product, has long been appreciated for its capacity to add complexity to eukaryotic proteomes. However, evidence suggests that the utility of this process extends beyond protein output and provides cells with a dynamic tool for gene regulation. In this review, we aim to highlight the role that intronic RNA plays in mediating specific splicing outcomes in pre-mRNA processing, as well as explore an emerging class of stable intronic sequences that have been observed to act in gene expression control. Building from underlying flexibility in both sequence and structure, intronic RNA provides mechanisms for post-transcriptional gene regulation that are amenable to the tissue and condition specific needs of eukaryotic cells. This article is part of a Special Issue entitled: RNA structure and splicing regulation edited by Francisco Baralle, Ravindra Singh and Stefan Stamm.
RNA 剪接是一种将非编码 RNA(内含子)的中间片段从前体 mRNA 中切除,从而形成成熟 mRNA 产物的过程,长期以来一直因其能够为真核生物蛋白质组增加复杂性而受到重视。然而,有证据表明,这一过程的用途不仅限于蛋白质输出,还为细胞提供了一种用于基因调控的动态工具。在这篇综述中,我们旨在强调内含子 RNA 在介导前体 mRNA 加工过程中特定剪接结果方面的作用,并探索一类新兴的稳定内含子序列,这些序列被观察到在基因表达调控中发挥作用。基于序列和结构的内在灵活性,内含子 RNA 提供了适用于真核细胞组织和条件特异性需求的转录后基因调控机制。本文是由 Francisco Baralle、Ravindra Singh 和 Stefan Stamm 编辑的题为“RNA 结构和剪接调控”的特刊的一部分。