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编辑转录组:检测核苷酸脱氨酶的新型高通量方法。

The edited transcriptome: novel high throughput approaches to detect nucleotide deamination.

机构信息

Department of Molecular Biology & Functional Genomics, Stockholm University, SE-106 91 Stockholm, Sweden.

出版信息

Curr Opin Genet Dev. 2011 Aug;21(4):401-6. doi: 10.1016/j.gde.2011.04.009. Epub 2011 May 14.

Abstract

RNA editing is emerging as a wide-spread phenomenon both in coding and non-coding RNA regions. While the mechanisms underlying many of these post-transcriptional modifications have not been elucidated, RNA editing by nucleotide deamination has been known for over two decades as a mechanism to generate base substitutions. With the recently growing use of high throughput sequencing technologies, knowledge about the frequency and diversity of RNA nucleotide substitutions has vastly increased. In this review we will highlight recent findings within this field, and illustrate how novel technologies have made it possible to detect and measure the efficiency of editing in an unprecedented accuracy and robustness. Future prospects for the detection of important transcriptome variations will also be discussed.

摘要

RNA 编辑在编码和非编码 RNA 区域都呈现出广泛存在的现象。虽然许多这些转录后修饰的机制尚未阐明,但核苷酸脱氨酶介导的 RNA 编辑作为一种产生碱基替换的机制已被人们熟知超过二十年。随着高通量测序技术的广泛应用,关于 RNA 核苷酸替换的频率和多样性的知识已经大大增加。在这篇综述中,我们将重点介绍该领域的最新发现,并说明新技术如何以前所未有的准确性和稳健性来检测和衡量编辑效率。我们还将讨论检测重要转录组变异的未来前景。

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