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检测 mRNA 修饰的错配掺入特征:并不像听起来那么简单。

Misincorporation signatures for detecting modifications in mRNA: Not as simple as it sounds.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Methods. 2019 Mar 1;156:53-59. doi: 10.1016/j.ymeth.2018.10.011. Epub 2018 Oct 23.

Abstract

Post-transcriptional modification on mRNA has become a field of intense interest in recent years, and next-generation sequencing based technologies are constantly emerging to detect an increasing number of modifications at a transcriptome-wide level. Some of these approaches are based on identification of misincorporation events induced by reverse transcriptase at modified sites. Although conceptually trivial, sensitive and specific identification of such events is a challenge prone to a surprising number of artifacts, which can lead to substantially inflated estimates of the abundance of diverse modifications. Here we discuss the sources of some of these artifacts and delineate approaches to overcome them.

摘要

近年来,mRNA 的转录后修饰已成为一个研究热点,基于下一代测序的技术不断涌现,以在转录组范围内检测越来越多的修饰。其中一些方法基于识别逆转录酶在修饰位点引起的错配事件。尽管从概念上讲微不足道,但此类事件的灵敏和特异性识别具有挑战性,容易产生大量的假象,这可能导致对各种修饰丰度的估计大大膨胀。在这里,我们讨论了其中一些假象的来源,并阐明了克服这些假象的方法。

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