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大规模预测 ADAR 介导的有效的人类 A-to-I RNA 编辑。

Large-scale prediction of ADAR-mediated effective human A-to-I RNA editing.

机构信息

Department of Gastroenterology, Zhongshan Hospital of Fudan University, Shanghai, China.

College of Life Science, Northeast Forestry University, Harbin, China.

出版信息

Brief Bioinform. 2019 Jan 18;20(1):102-109. doi: 10.1093/bib/bbx092.

Abstract

Adenosine-to-inosine (A-to-I) editing by adenosine deaminase acting on the RNA (ADAR) proteins is one of the most frequent modifications during post- and co-transcription. To facilitate the assignment of biological functions to specific editing sites, we designed an automatic online platform to annotate A-to-I RNA editing sites in pre-mRNA splicing signals, microRNAs (miRNAs) and miRNA target untranslated regions (3' UTRs) from human (Homo sapiens) high-throughput sequencing data and predict their effects based on large-scale bioinformatic analysis. After analysing plenty of previously reported RNA editing events and human normal tissues RNA high-seq data, >60 000 potentially effective RNA editing events on functional genes were found. The RNA Editing Plus platform is available for free at https://www.rnaeditplus.org/, and we believe our platform governing multiple optimized methods will improve further studies of A-to-I-induced editing post-transcriptional regulation.

摘要

腺苷到肌苷(A 到 I)编辑由 RNA 上的腺苷脱氨酶作用(ADAR)蛋白在转录后和共转录过程中是最常见的修饰之一。为了将生物学功能分配给特定的编辑位点,我们设计了一个自动在线平台,用于注释人类(Homo sapiens)高通量测序数据中前体 mRNA 剪接信号、微小 RNA(miRNA)和 miRNA 靶标非翻译区(3'UTR)中的 A 到 I RNA 编辑位点,并基于大规模生物信息学分析预测其影响。在分析了大量先前报道的 RNA 编辑事件和人类正常组织 RNA 高测序数据后,在功能基因上发现了 >60000 个潜在有效的 RNA 编辑事件。RNA Editing Plus 平台可在 https://www.rnaeditplus.org/ 免费使用,我们相信我们的平台管理多种优化方法将进一步改善 A 到 I 诱导的编辑转录后调控的研究。

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