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基于计算方法的剪接调控 RNA 结构发现

Computational approaches for the discovery of splicing regulatory RNA structures.

机构信息

Roy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, 2437 Pammel Drive, Ames, IA 50011, USA.

Roy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, 2437 Pammel Drive, Ames, IA 50011, USA.

出版信息

Biochim Biophys Acta Gene Regul Mech. 2019 Nov-Dec;1862(11-12):194380. doi: 10.1016/j.bbagrm.2019.04.007. Epub 2019 Apr 29.

Abstract

Global RNA structure and local functional motifs mediate interactions important in determining the rates and patterns of mRNA splicing. In this review, we overview approaches for the computational prediction of RNA secondary structure with a special emphasis on the discovery of motifs important to RNA splicing. The process of identifying and modeling potential splicing regulatory structures is illustrated using a recently-developed approach for RNA structural motif discovery, the ScanFold pipeline, which is applied to the identification of a known splicing regulatory structure in influenza virus.

摘要

全球 RNA 结构和局部功能基序介导了决定 mRNA 剪接速率和模式的重要相互作用。在这篇综述中,我们概述了计算预测 RNA 二级结构的方法,特别强调了发现对 RNA 剪接重要的基序。使用最近开发的 RNA 结构基序发现方法 ScanFold 管道来识别和建模潜在的剪接调节结构的过程,该方法应用于鉴定流感病毒中的已知剪接调节结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca2/6819252/fab724af28c6/nihms-1528821-f0001.jpg

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