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一个用于高通量分析 RNA 序列和通过质谱法进行修饰的计算平台。

A computational platform for high-throughput analysis of RNA sequences and modifications by mass spectrometry.

机构信息

Epigenetics Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Center for Bioinformatics Tübingen, University of Tübingen, Tübingen, Germany.

出版信息

Nat Commun. 2020 Feb 17;11(1):926. doi: 10.1038/s41467-020-14665-7.

Abstract

The field of epitranscriptomics continues to reveal how post-transcriptional modification of RNA affects a wide variety of biological phenomena. A pivotal challenge in this area is the identification of modified RNA residues within their sequence contexts. Mass spectrometry (MS) offers a comprehensive solution by using analogous approaches to shotgun proteomics. However, software support for the analysis of RNA MS data is inadequate at present and does not allow high-throughput processing. Existing software solutions lack the raw performance and statistical grounding to efficiently handle the numerous modifications found on RNA. We present a free and open-source database search engine for RNA MS data, called NucleicAcidSearchEngine (NASE), that addresses these shortcomings. We demonstrate the capability of NASE to reliably identify a wide range of modified RNA sequences in four original datasets of varying complexity. In human tRNA, we characterize over 20 different modification types simultaneously and find many cases of incomplete modification.

摘要

表观转录组学领域不断揭示 RNA 的转录后修饰如何影响广泛的生物学现象。该领域的一个关键挑战是在其序列背景中鉴定修饰 RNA 残基。质谱 (MS) 通过采用类似的方法对蛋白质组进行分析,提供了一个全面的解决方案。然而,目前用于 RNA MS 数据分析的软件支持不足,无法进行高通量处理。现有的软件解决方案缺乏原始性能和统计学基础,无法有效地处理 RNA 上发现的众多修饰。我们提出了一种用于 RNA MS 数据的免费开源数据库搜索引擎,称为 NucleicAcidSearchEngine (NASE),它解决了这些缺点。我们证明了 NASE 能够可靠地鉴定四个不同复杂程度的原始数据集的广泛修饰 RNA 序列。在人 tRNA 中,我们同时表征了 20 多种不同的修饰类型,并发现了许多修饰不完全的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a6/7026122/9df710e10ffe/41467_2020_14665_Fig1_HTML.jpg

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